US20120130532A1 - Medicine dispensing system and medicine dispensing device - Google Patents
Medicine dispensing system and medicine dispensing device Download PDFInfo
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- US20120130532A1 US20120130532A1 US13/364,210 US201213364210A US2012130532A1 US 20120130532 A1 US20120130532 A1 US 20120130532A1 US 201213364210 A US201213364210 A US 201213364210A US 2012130532 A1 US2012130532 A1 US 2012130532A1
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- Prior art keywords
- medicine
- container
- medicine feeding
- medicines
- feeding container
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
- A61J7/00—Devices for administering medicines orally, e.g. spoons; Pill counting devices; Arrangements for time indication or reminder for taking medicine
- A61J7/0076—Medicament distribution means
- A61J7/0084—Medicament distribution means for multiple medicaments
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65B—MACHINES, APPARATUS OR DEVICES FOR, OR METHODS OF, PACKAGING ARTICLES OR MATERIALS; UNPACKING
- B65B37/00—Supplying or feeding fluent-solid, plastic, or liquid material, or loose masses of small articles, to be packaged
- B65B37/16—Separating measured quantities from supply
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
- A61J3/00—Devices or methods specially adapted for bringing pharmaceutical products into particular physical or administering forms
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65B—MACHINES, APPARATUS OR DEVICES FOR, OR METHODS OF, PACKAGING ARTICLES OR MATERIALS; UNPACKING
- B65B1/00—Packaging fluent solid material, e.g. powders, granular or loose fibrous material, loose masses of small articles, in individual containers or receptacles, e.g. bags, sacks, boxes, cartons, cans, or jars
- B65B1/04—Methods of, or means for, filling the material into the containers or receptacles
- B65B1/16—Methods of, or means for, filling the material into the containers or receptacles by pneumatic means, e.g. by suction
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65B—MACHINES, APPARATUS OR DEVICES FOR, OR METHODS OF, PACKAGING ARTICLES OR MATERIALS; UNPACKING
- B65B5/00—Packaging individual articles in containers or receptacles, e.g. bags, sacks, boxes, cartons, cans, jars
- B65B5/10—Filling containers or receptacles progressively or in stages by introducing successive articles, or layers of articles
- B65B5/101—Filling containers or receptacles progressively or in stages by introducing successive articles, or layers of articles by gravity
- B65B5/103—Filling containers or receptacles progressively or in stages by introducing successive articles, or layers of articles by gravity for packaging pills or tablets
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65B—MACHINES, APPARATUS OR DEVICES FOR, OR METHODS OF, PACKAGING ARTICLES OR MATERIALS; UNPACKING
- B65B57/00—Automatic control, checking, warning, or safety devices
- B65B57/10—Automatic control, checking, warning, or safety devices responsive to absence, presence, abnormal feed, or misplacement of articles or materials to be packaged
- B65B57/14—Automatic control, checking, warning, or safety devices responsive to absence, presence, abnormal feed, or misplacement of articles or materials to be packaged and operating to control, or stop, the feed of articles or material to be packaged
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65B—MACHINES, APPARATUS OR DEVICES FOR, OR METHODS OF, PACKAGING ARTICLES OR MATERIALS; UNPACKING
- B65B61/00—Auxiliary devices, not otherwise provided for, for operating on sheets, blanks, webs, binding material, containers or packages
- B65B61/02—Auxiliary devices, not otherwise provided for, for operating on sheets, blanks, webs, binding material, containers or packages for perforating, scoring, slitting, or applying code or date marks on material prior to packaging
- B65B61/025—Auxiliary devices, not otherwise provided for, for operating on sheets, blanks, webs, binding material, containers or packages for perforating, scoring, slitting, or applying code or date marks on material prior to packaging for applying, e.g. printing, code or date marks on material prior to packaging
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- G—PHYSICS
- G07—CHECKING-DEVICES
- G07F—COIN-FREED OR LIKE APPARATUS
- G07F11/00—Coin-freed apparatus for dispensing, or the like, discrete articles
- G07F11/02—Coin-freed apparatus for dispensing, or the like, discrete articles from non-movable magazines
- G07F11/04—Coin-freed apparatus for dispensing, or the like, discrete articles from non-movable magazines in which magazines the articles are stored one vertically above the other
- G07F11/16—Delivery means
- G07F11/165—Delivery means using xyz-picker or multi-dimensional article picking arrangements
-
- G—PHYSICS
- G07—CHECKING-DEVICES
- G07F—COIN-FREED OR LIKE APPARATUS
- G07F11/00—Coin-freed apparatus for dispensing, or the like, discrete articles
- G07F11/02—Coin-freed apparatus for dispensing, or the like, discrete articles from non-movable magazines
- G07F11/04—Coin-freed apparatus for dispensing, or the like, discrete articles from non-movable magazines in which magazines the articles are stored one vertically above the other
- G07F11/16—Delivery means
- G07F11/165—Delivery means using xyz-picker or multi-dimensional article picking arrangements
- G07F11/1657—Delivery means using xyz-picker or multi-dimensional article picking arrangements the picking arrangements using suction
-
- G—PHYSICS
- G07—CHECKING-DEVICES
- G07F—COIN-FREED OR LIKE APPARATUS
- G07F11/00—Coin-freed apparatus for dispensing, or the like, discrete articles
- G07F11/46—Coin-freed apparatus for dispensing, or the like, discrete articles from movable storage containers or supports
- G07F11/50—Coin-freed apparatus for dispensing, or the like, discrete articles from movable storage containers or supports the storage containers or supports being rotatably mounted
- G07F11/54—Coin-freed apparatus for dispensing, or the like, discrete articles from movable storage containers or supports the storage containers or supports being rotatably mounted about vertical axes
-
- G—PHYSICS
- G07—CHECKING-DEVICES
- G07F—COIN-FREED OR LIKE APPARATUS
- G07F17/00—Coin-freed apparatus for hiring articles; Coin-freed facilities or services
- G07F17/0092—Coin-freed apparatus for hiring articles; Coin-freed facilities or services for assembling and dispensing of pharmaceutical articles
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
- G16H10/00—ICT specially adapted for the handling or processing of patient-related medical or healthcare data
- G16H10/60—ICT specially adapted for the handling or processing of patient-related medical or healthcare data for patient-specific data, e.g. for electronic patient records
-
- G—PHYSICS
- G16—INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR SPECIFIC APPLICATION FIELDS
- G16H—HEALTHCARE INFORMATICS, i.e. INFORMATION AND COMMUNICATION TECHNOLOGY [ICT] SPECIALLY ADAPTED FOR THE HANDLING OR PROCESSING OF MEDICAL OR HEALTHCARE DATA
- G16H20/00—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance
- G16H20/10—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients
- G16H20/13—ICT specially adapted for therapies or health-improving plans, e.g. for handling prescriptions, for steering therapy or for monitoring patient compliance relating to drugs or medications, e.g. for ensuring correct administration to patients delivered from dispensers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
- A61J7/00—Devices for administering medicines orally, e.g. spoons; Pill counting devices; Arrangements for time indication or reminder for taking medicine
- A61J7/0069—Trays for holding or distributing medicines
Abstract
There is provided a medicine dispensing system configured such that a medicine dispensing device includes a sub unit having a function to dispense medicine that is connected to a medicine dispensing device that includes a main unit having a function of packing medicines. There is also provided a medicine dispensing device that can be appropriately integrated with such a medicine dispensing system. The medicine dispensing system includes, in some embodiments a main unit, a sub unit and a transfer device connecting the main unit and the sub unit. The medicine dispensing system transfers the medicine dispensed in the sub unit to the main unit by means of a transfer device and dispenses the medicine at a medicine packing part together with the medicine dispensed from a main storage part in the main unit.
Description
- This application is a continuation of U.S. application Ser. No. 12/765,741, filed Apr. 22, 2010, which is a continuation-in-part under 35 U.S.C. §§120 and 365(c) of International Patent Application No. PCT/JP2008/069208, filed Oct. 23, 2008, the entire contents of both of which are incorporated by reference herein, which claims the benefit of the following applications, the entire contents of each of which are incorporated by reference herein:
- Japanese Patent Application No. 2007-274931, filed Oct. 23, 2007,
- Japanese Patent Application No. 2007-274932, filed Oct. 23, 2007,
- Japanese Patent Application No. 2007-274933, filed Oct. 23, 2007,
- Japanese Patent Application No. 2007-274934, filed Oct. 23, 2007,
- Japanese Patent Application No. 2008-190195, filed Jul. 23, 2008,
- Japanese Patent Application No. 2008-240590, filed Sep. 19, 2008, and
- Japanese Patent Application No. 2008-264662, filed Oct. 10, 2008.
- The present invention relates to a medicine dispensing system constructed by adding a sub unit to a main unit. Further, the present invention relates to a medicine dispensing device for such a sub unit.
- There exists in the art a medicine dispensing device as disclosed in the below-mentioned
reference Patent Document 1. A prior art medicine dispensing device has a storage part for storing a plurality kinds of medicines. Such a prior art medicine dispensing device is constructed to pack medicines removed from the storage part according to prescriptions and dispense the same. - Patent Document 1: Japanese Laid-Open Patent Application No. 2001-276183
- In a prior art medicine dispensing device, the storage part is configured to accommodate a plurality kinds of medicines. However, with an increase in the kinds of medicines to be dealt with, more kinds of medicines than those accommodated by the storage part must be dealt with. Installing a plurality of prior art medicine dispensing devices can address such a need. However, there is a problem with such solution in that each medicine dispensing device packs medicines in a different manner. Further, installing a plurality of medicine dispensing devices has another problem in that it needs a larger installation area resulting in higher maintenance costs.
- In one embodiment, a medicine dispensing system is configured such that a medicine dispensing device includes a sub unit having a function of dispensing medicines that is connected to a medicine dispensing device that includes a main unit having a function of packing medicines. The present invention also seeks to provide a medicine dispensing device that can be appropriately employed to such a medicine dispensing system.
- In another embodiment, a medicine dispensing system includes a main unit; one or more sub units; and a transfer device configured to connect the main unit and the sub units. The main unit includes: a main storage part configured to store and dispense a plurality kinds of medicines; and a packing part configured to pack the medicine dispensed from the main storage part. The sub unit includes a sub storage part configured to store and dispense a plurality kinds of medicines. The transfer device transfers the medicine dispensed from the sub storage part toward the main unit. The packing part of the main unit packs and dispenses the medicine.
- The medicine dispensing system of the present invention includes the main unit and the sub unit and can transfer the medicine dispensed from the sub storage part provided in the sub unit toward the main unit using the transfer device. Further, in the medicine dispensing system of the present invention, the main unit has the packing part. The main unit can pack not only the medicine dispensed from the main storage part of the main unit, but also the medicine from the sub storage part of the sub unit at the pack part. Thus, the medicine dispensing system of the present invention can deal with many kinds of medicines and a large quantity of medicine through use of the sub unit when compared to utilizing the main unit alone.
- Further, the packing part of the main unit is capable of packing the medicine dispensed in the sub unit. Thus, the medicines dispensed from both the main unit and the sub unit can be packed into equal medicine packs or containers. Further, the medicine dispensing system of the present invention does not need a packing part to be included in the sub unit. Thus, not providing a packing part to the sub unit allows the sub unit to be compact or to be configured to accommodate more kinds of medicines and a larger quantity of medicine. Moreover, this can minimally decrease the installation area of the medicine dispensing system as well as the maintenance task thereof.
- Further, the transfer device of the medicine dispensing system may have the pipe line connecting the main unit and the sub unit and the transfer means configured to suck or pressure-send the medicine staying in the pipe line from the sub unit toward the main unit.
- According to such configuration, the medicines dispensed from the sub storage part in the sub unit may be easily transferred to the main unit.
- The transfer device, which the medicine dispensing system of some embodiments includes, is configured to suck or pressure-send medicines existing in the pipe line by means of the medicine transfer means. Thus, according to the above-described transfer device, medicines can be rapidly transferred from the sub unit toward the main unit. Further, the above-described transfer device is capable of a transfer path of the medicines by appropriately adjusting the shape of the pipe line. Thus, the medicine dispensing system of in an embodiment has a higher degree of freedom in arrangement on the main unit and the sub unit.
- Further, the transfer path of the transfer means can be set by appropriately adjusting the pipe line. Thus, it is possible to appropriately set the dispensing position of the medicine transferred by the transfer device in the main unit and the delivery position of delivering the medicine to be transferred to the transfer device. Accordingly, layout and configuration of members or components making up the main unit and the sub unit can be adjusted independently and respectively. Specifically, in the medicine dispensing system of one embodiment, the layout and configuration of the sub storage part of the sub unit can be adjusted to be adapted to the medicine storage or the medicine dispensing independently of the layout and configuration of the main storage part, a medicine awaiting part, the packing part, etc. Thus, in the medicine dispensing system of the present invention, it is possible to optimize the layout and configuration of the main unit and the sub unit.
- Further, the transfer device may have a medicine delivering part configured to receive and dispense a medicine. The medicine delivering part may be configured to turn about a turning shaft and expand and contract in a direction orthogonal to the turning shaft.
- The transfer device, in some embodiments, has the medicine delivering part configured to receive and dispense a medicine. The medicine delivering part is configured to turn about the turning shaft and expand and contract in the direction orthogonal to the turning shaft. Thus, the medicine dispensing system in some embodiments is capable of receiving the medicine dispensed in the sub unit and delivering the same to the main unit by appropriately turning the medicine delivering part or expanding and contracting the medicine delivering part according to the arrangement of the main unit and the sub unit.
- The medicine dispensing system of the present invention can appropriately adjust the arrangement of the main unit and the sub unit within a range wherein the medicine can be delivered by the transfer means. Thus, the medicine dispensing system of the present invention has a higher degree of freedom in the arrangement of the main unit and the sub unit. Further, the medicine delivering part is capable of turning and expanding and contracting in the direction orthogonal to the turning shaft. Thus, the medicine delivering part can turn as contracted and therefore a space necessary for turning of the medicine delivering part can be minimized. Accordingly, the present invention can contribute saving space in the medicine dispensing system.
- Further, the transfer device may include a medicine delivery container configured to receive and dispense a medicine; and a drive mechanism configured to move the medicine delivery container between the main unit and the sub unit. The drive mechanism may include a conveying part configured to reciprocate the medicine delivering part; a direction adjusting means configured to adjust a direction of the conveying means relative to the main unit and the sub unit by turning the conveying means.
- The transfer device, which is employed in the present invention, is configured to reciprocate the medicine delivery container for receiving and dispensing a medicine in the conveying part and to adjust the direction thereof relative to the main unit and the sub unit by turning the conveying part. Thus, in the medicine dispensing system of the present invention, the medicine dispensed in the sub unit can be received into the medicine delivering part by adjusting the inclined direction of the delivering part such that the medicine dispensed from the sub storage part of the sub unit is situated in a position where the medicine can be received. Further, the medicine dispensed in the sub unit can be delivered to the main unit by adjusting an inclination of a conveyance path such that the medicine delivery container reaches a position where the medicine is delivered in the main storage part after the medicine is received in the medicine delivering part, and then by moving the medicine delivering part to the main unit.
- The medicine dispensing system in some embodiments can appropriately adjust the arrangement of the main unit and the sub unit within a range wherein the medicine can be delivered by the transfer means. Thus, the medicine dispensing system can appropriately adjust the arrangement of the main unit and the sub unit.
- Further, the transfer device may include a forward pipe line connecting the main storage part and the sub storage part; an airflow producing means producing airflow from the sub unit toward the main unit within the forward pipe line; an exhaust pipe line connected to the main storage part; a suction and exhaust means sucking and exhausting through the exhaust pipe line from an inside portion of the main storage part to an outside portion thereof; and a shutter disposed between the forward pipe line and the exhaust pipe line and the main storage part. The transfer device may be configured to perform the following: a medicine transferring operation for moving a medicine to the main storage part by operating the airflow producing means in a closed state where the forward pipe line is closed by the shutter; and a medicine introducing operation for introducing a medicine from the forward pipe line to the main storage part by operating the airflow producing means in a communication state where the shutter is opened and the forward pipe line, the exhaust pipe line and the main storage part are in communication with one another.
- The medicine dispensing system can transfer medicine from the sub storage part toward the main storage part through the medicine transferring operation and thereafter can introduce the medicine transferred in such a manner to the main storage part through the medicine introducing operation. Thus, the medicine dispensing system of the present invention can deliver the medicine from the sub storage part to the main storage part by repeating the above-described medicine transferring operation and medicine introducing operations.
- Further, in the medicine dispensing system of the present invention, since the operation for transferring the medicine between the main unit and the sub unit and the operation for introducing the medicine in the main unit are separately performed, the velocity of the airflow flowing within the forward pipe line during transfer of the medicine may be not so fast. Thus, in the medicine dispensing system of on embodiment, the medicines transferred from the main unit to the sub unit can be prevented from severely colliding with each other, breaking or chipping during their transfer.
- In the above-described medicine dispensing system, the shutter may include a forward obstruction portion for obstructing a space between the forward pipe line and the main storage part; and a buffer means provided at the forward obstruction portion and configured to buffer an impact caused by a collision of the medicines proceeding within the forward pipe line.
- With the above-described construction, the buffer means buffers the impact caused by a collision of the medicines with the shutter in the medicine transferring operation. Thus, the medicine dispensing system of the present invention can surely prevent the medicines from breaking or chipping due to collisions with the shutter in the medicine transferring operation.
- The above-described medicine dispensing system may include a partitioning means configured to partition an internal space of the main storage part. Further, the medicine dispensing system may be configured such that when the shutter becomes opened, both the exhaust pipe line and the forward pipe line become in communication with a space, which is formed according to a division caused by the partitioning means.
- The above-described medicine dispensing system can decrease the volume of the space, with which, when the shutter becomes opened, both the exhaust pipe line and the forward pipe line become in communication with each other, by partitioning the internal space of the main storage part through the partitioning means. Thus, the above-described medicine dispensing system does not need to excessively enlarge the exhaust capacity of the suction and exhaust means in order to introduce the medicine from the forward pipe line to the main storage part in the medicine introducing operation. Further, according to the above-described configuration, the exhaust capacity of the suction and exhaust means can be restricted. Thus, when the medicines are introduced to the main storage part, it is possible to prevent the medicines from colliding into one another and colliding with an inner peripheral surface of the main storage part or to buffer the impact resulting from such collision. Further, it is possible to more certainly prevent occurrence of the breakage or chipping of the medicines along with the medicine transfer.
- In the above-described medicine dispensing system, it is preferred that the velocity of airflow flowing to transfer the medicine toward the main unit in the medicine transferring operation is slower than that of the airflow flowing to introduce the medicine to the main unit in the medicine introducing operation.
- According to such configuration, it is possible to certainly prevent the medicine transferred from the sub unit through the medicine transferring operation from colliding with the shutter to thereby break.
- In the above-described medicine dispensing system, the exhaust pipe line may connect the main storage part and the sub storage part.
- The above-described medicine dispensing system may include a filter provided at a halfway portion of a flow line wherein airflow is produced concomitantly with transferring the medicine between the sub storage part and the main storage part; an airflow amount detecting means configured to detect an airflow amount in the flow line concomitantly with transferring the medicine from the main storage part to the sub storage part; and a clogging judging means configured to judge a clogging of the filter based on the airflow amount detected by the airflow amount detecting means.
- According to such configuration, the clogging of the filter can be easily and certainly detected and thus maintenance of the filter can be performed at an appropriate time.
- In case of employing such configuration, when it is doubtful whether the filter is clogged due to a decrease in the airflow amount detected by the airflow amount detecting means, the clogging judging means may judge the clogging of the filter and then the operation for transferring the medicine may be immediately stopped. If so, the medicine stops in the middle of the forward pipe line, thereby leading to troubles in the dispensing operation. Therefore, although the filter could be possibly clogged, it is preferred that the medicine dispensing system is configured to transfer the medicine to the main storage part.
- Further, it is more preferable that the medicine dispensing system is configured to transfer the medicine to the main storage part by increasing the output of the airflow producing means and/or the suction and exhaust means when there is a decrease in the airflow amount detected by the airflow amount detecting means, and to judge the clogging of the filter by the clogging detecting means upon when there is an increase in the output of the airflow producing means and/or the suction and exhaust means.
- When the medicine dispensing system is configured as indicated above, it is possible in some embodiments to transfer the medicine to the main storage part prior to judging the clogging of the filter by increasing the output of the airflow producing means or the suction and exhaust means. Thus, according to such configuration, it is possible to prevent problems during the dispensing operation, which may occur because the medicines stop in the middle of the forward pipe line due to the clogging of the filter.
- The above-described medicine dispensing system may include a filter provided at a halfway portion of a flow line wherein airflow is produced concomitantly with transferring the medicine between the sub storage part and the main storage part; an airflow amount detecting means configured to detect an airflow amount in the flow line concomitantly with transferring the medicine from the main storage part to the sub storage part; and a notifying means. The medicine dispensing system may be configured to transfer the medicine to the main storage part by increasing the output of the airflow producing means and/or the suction and exhaust means upon a condition of decrease in the airflow amount detected by the airflow amount detecting means, and to notify the clogging of the filter by the notifying means.
- Where the medicine dispensing system is configured as indicated above, when it is assumed that the filter is clogged due to a decrease in the airflow amount detected by the airflow amount detecting means, the medicine under the transferring operation is transferred, in some embodiments, to the main storage part and at the same time, the clogging of the filter is immediately notified, thereby urging users to take suitable measures.
- Further, according to the present invention, the transfer device may include a forward pipe line connecting the main storage part and the sub storage part; an airflow producing means configured to produce an air flow within the forward pipe line from the sub unit toward the main unit; and a delivery part connected to the forward pipe line and configured to receive and dispense the medicine transferred from the sub unit through the forward pipe line in the main unit. The delivery part may include a delivery container, to which the forward pipe line is connected, and a shutter. The delivery container may include an internal space, which is configured such that the medicine transferred through the forward pipe line freely falls therein, and a dispensing opening disposed at a bottom portion of the delivery container to dispense the medicine. The shutter may be configured to be changed between a dispensing-allowed state where the medicine is allowed to be dispensed from the dispensing opening, and a dispensing-unallowed state.
- In the medicine dispensing system of another embodiment, the medicine dispensed from the sub storage part may be transferred to the main storage part and may be received in the delivering part in advance, by having the shutter being in the dispensing-unallowed state where the medicine is not dispensed from the dispensing opening formed at the bottom of the delivering part and by operating the airflow producing means. Thereafter, the medicine received in the delivering part may be dispensed for a purpose of packing it by operating the shutter and converting it in the dispensing-unallowed state where the medicine is dispensed from the dispensing opening. Thus, the medicine dispensing system of the present invention may pack the medicine dispensed from the main storage part as well as the medicine dispensed from the sub storage part at the packing part provided in the main unit.
- Meanwhile, in case the forward pipe line is connected to the delivering part as described above, since the medicine transferred from the sub unit is moved within the delivery container due to the airflow flowing from the forward pipe line into the delivery container, there could be a possibility that the medicine does not freely drop toward the bottom of the delivery container formed with the dispensing opening.
- Accordingly, according to the present invention provided considering such knowledge, the delivery container may include an exhaust hole for exhausting an airflow flowing in through the forward pipe line and the exhaust hole may be positioned downwardly of a connection position between the delivery container and the forward pipe line.
- In the medicine dispensing system of the present invention, since the exhaust hole is positioned downwardly of the connection position between the delivery container and the forward pipe line, the airflow flowing into the delivery container through the forward pipe line is allowed to flow downwardly. Thus, the medicine introduced into the delivery container through the forward pipe line also drops smoothly along with the airflow flowing downwardly within the delivery container.
- In the above-described medicine dispensing system, the delivery container may include a side portion (A) connected to the forward pipe line; and a pair of opposed side portions (B, C) crossing to the side portions. The exhaust hole may be provided at each of the pair of the side portions (B, C).
- Where the medicine dispensing system is configured as such, the airflow flowing into the delivery container through the forward pipe line is allowed to bifurcately flow to the exhaust holes provided at the side portions (B, C) and thus the medicine smoothly drops within the delivery container.
- When the medicine is introduced into the delivering part along with the airflow flowing through the forward pipe line as described above, there could be a possibility that the medicine collides against an inner wall surface of the delivery container from the force of the airflow. Thus, the above-described medicine dispensing system is configured to minimize the impact on the medicine caused by its collision.
- Accordingly, considering such knowledge, a buffer means configured to buffer an impact caused by collision of the medicine may be provided within the delivery container. The forward pipe line may be connected to a side portion of the delivery container, and the buffer means may be disposed opposite to the side portion to which the forward pipe line is connected.
- In the medicine dispensing system of the present invention, the buffer means is disposed within the delivery container opposite to the side portion to which the forward pipe line is connected. Thus, when the medicine introduced into the delivery container from the forward pipe line flows on the force of the airflow and collides against the buffer means, the impact caused thereby is buffered and the possibility of breakage or chipping of the medicine is reduced.
- Further, the shutter may be configured to change an inclination thereof in the delivery container. The shutter may go into the dispensing-unallowed state where the medicine is not dispensed from the dispensing opening when the shutter is situated to obliquely traverse the internal space of the delivery container. And, the shutter may go into the dispensing-allowed state where the medicine is dispensed from the dispensing opening by changing the inclination of the shutter from the dispensing-unallowed state.
- In the dispensing-unallowed state where the medicine is not dispensed from the dispensing opening, the shutter is inclined within the delivery container. Thus, according to such configuration, a dropping distance of the medicine within the delivery container can be shortened and the medicine dropping down toward the shutter can be guided to the bottom side along the shutter, thereby minimizing the impact exerted on the medicine.
- In the above-described medicine dispensing system, the delivery container may be configured to be divided into two or more sub container bodies.
- According to such configuration, since the delivery container is divided into each sub container body, cleaning the inside of the delivery container and the maintenance thereof can be easily performed.
- If the airflow is produced to flow toward the delivering part to transfer the medicine from the sub unit to the main unit as described above, it is preferable to devise some means so that dust cannot blow in undesired locations due to the airflow exhausted from the delivering part.
- Accordingly, the delivery part may further include an outer container, in which the delivery container may be disposed. The delivery container may include an exhaust part for exhausting an airflow exhausted from the delivery container into the outer container outwardly of the outer container.
- In some embodiments, the delivery container is disposed in the outer container and the airflow exhausted from the delivery part can be exhausted through the exhausting part into an internal space of the outer container. Thus, it is possible to prevent the dusts from blowing under the influence caused by the exhausted airflow.
- Further, in other embodiments, the exhausting part may include a primary filter; and a secondary filter disposed downstream of the primary filter in an exhaust flow direction, the secondary filter having meshes finer than the primary filter.
- In the medicine dispensing system of the present invention, since the primary filter and the secondary filter are provided at the exhausting part, when dusts is contained in the airflow exhausted from the delivering part to the outer container, such dust can be prevented from leaking outwardly of the outer container. Further, in the medicine dispensing system of the present invention, the primary filter with sparse meshes is disposed upstream of the secondary filter having fine meshes in the exhaust flow direction, thereby enlarging a service life of the secondary filter with fine meshes.
- Further, in the above-described medicine dispensing system, a piping constituting the forward pipe line may preferably comprise a hard material in order to prevent jamming caused by the medicine in the middle thereof. Meanwhile, when the forward pipe line comprising a piping of a hard material is directly connected to the delivering part, a joint portion between the forward pipe line and the delivering part can be broken due to some stress acting thereon. Thus, in the above-described medicine dispensing system, it is preferable to devise some means to cope with such a problem.
- Accordingly, the delivery container and the forward pipe line may be connected to each other via a flexible joint pipe.
- According to such configuration, when some stress acts on the forward pipe line, such stress is absorbed or mitigated through the joint pipe constituting the joint portion between the delivering part and the forward pipe line, thereby preventing the joint portion between the delivering part and the forward pipe line from being broken.
- In the above-described medicine dispensing, while a transfer operation of medicine from the sub unit to the main unit is completed and thereafter a next transfer operation is done, the shutter may go into the dispensing-allowed state and the airflow producing means may operate, thereby performing a sweeping operation for sweeping a medicine transfer passage formed in the transfer device.
- According to such configuration, the medicine transfer passage formed in the transfer device can be maintained cleanly with ease.
- According to another embodiment, a medicine dispensing device for a sub unit for constructing a medicine dispensing system includes a main unit and one or more sub units, the main unit and the sub unit being configured to dispense a predetermined medicine by a predetermined quantity; and a transfer device, wherein a medicine dispensed in the sub unit is transferred by the transfer device to the main unit and is dispensed in the main unit. The medicine dispensing device may include a sub storage part configured to store and dispense a plurality kinds of medicines; and a transfer device configured to transfer a medicine dispensed from the sub storage part toward the main unit.
- The medicine dispensing device includes the transfer device and is configured to dispense medicine from the sub storage part toward the main storage part by means of the transfer device. Thus, a medicine dispensing system may be constructed, wherein the medicine stored in the sub storage part can be dispensed in the main unit, by employing the medicine dispensing device of the present invention as the sub unit and combining such a sub unit with the main unit.
- Further, in the medicine dispensing device of the present invention, the transfer device may have the pipe line connecting the main unit and the sub unit and the transfer means configured to suck or pressure-send the medicine staying in the pipe line from the sub unit toward the main unit.
- The medicine dispensing device can be a part of a medicine dispensing system, wherein the medicine dispensed from the sub storage part is fed to the main unit and can be dispensed in the main unit, by connecting the pipe line to the main unit.
- Further, since the above-described medicine dispensing device transfers the medicine by sucking or pressure-sending the medicine, a transfer path of the medicines can be appropriately set by appropriately arranging the pipe line. Thus, the medicine dispensing device may in some embodiments have a higher degree of freedom in arrangement on the main unit.
- Further, the transfer device may have a medicine delivering part configured to receive and dispense a medicine dispensed from the sub storage part. The medicine delivering part may be configured to turn about a turning shaft and expand and contract in a direction orthogonal to the turning shaft.
- The medicine dispensing device is configured such that the medicine delivering part turns about the turning shaft or expands and contracts in the direction orthogonal to the turning shaft. Thus, in case of combining the medicine dispensing device of the present invention with the main unit to construct a medicine dispensing system, the medicine delivering part can obtain its movable range and the medicine dispensed from the sub storage part to the medicine delivering part can be transferred to the main unit and be dispensed therefrom.
- Further, the medicine delivering part is capable of expanding and contracting in the direction orthogonal to the turning shaft. Thus, the medicine dispensing device of the present invention can turn the medicine delivering part as contracted. Therefore a space necessary for turning of the medicine delivering part can be minimized.
- Further, the transfer device may include a medicine delivery container configured to receive a medicine dispensed from the sub storage part and to dispense the medicine to a medicine preparing part for the medicine; and a drive mechanism configured to move the medicine delivery container between itself and the main unit. The drive mechanism may include a conveying part configured to reciprocate the medicine delivering part; a direction adjusting means configured to adjust a direction of the conveying means relative to the main unit by turning the conveying part.
- The transfer device, which is employed in the medicine dispensing device, has the drive mechanism and is configured to reciprocate the medicine delivery container between the main unit and itself and to adjust the direction of the conveying part relative to the main unit. Thus, the medicine dispensing device appropriately operates the transfer device to place the medicine delivery container in a position suitable for receiving the medicine dispensed in the sub unit and in a position where the medicine must be dispensed in the main unit.
- Further, the transfer device includes a forward pipe line in communication with the sub storage part and configured to be connected to the main storage part provided in the main unit; an airflow producing means producing airflow from the sub unit toward the main unit within the forward pipe line; an exhaust pipe line configured to be connected to the main storage part; a suction and exhaust means configured to suck and exhaust through the exhaust pipe line from inside the main storage part to an outside portion thereof; and a shutter configured to close at least one of the forward pipe line and the exhaust pipe line. The transfer device may be configured to perform the following: a medicine transferring operation for moving a medicine to the main storage part by operating the airflow producing means in a closed state where the forward pipe line is closed by the shutter; and a medicine introducing operation for introducing medicine from the forward pipe line to the main storage part by operating the suction and exhaust means in a communication state where the shutter is opened and the forward pipe line, the exhaust pipe line and the main storage part are in communication with one another.
- The medicine dispensing device can transfer a medicine by means of airflow flowing from the sub storage part toward the main storage part through the medicine transferring operation and thereafter can introduce the medicine into the main storage part through the medicine introducing operation. Thus, the medicine dispensing system of the present invention can deliver the medicine from the sub storage part to the main storage part by repeating the medicine transferring operation and medicine introducing operation.
- Further, in the medicine dispensing device, the medicine transferring operation for transferring the medicine by means of the airflow and the medicine introducing operation for introducing the medicine into the main storage part can be separately performed. Thus, in the medicine transferring operation, the airflow may flow within the forward pipe line at a velocity sufficient enough to transfer the medicine in the vicinity of the main storage part. The velocity of the airflow flowing within the forward pipe line in the medicine transferring operation does not need to become excessively fast. Thus, in the medicine dispensing system, the medicines transferred from the main unit to the sub unit can be prevented from severely colliding with each other, breaking or chipping during their transfer operation.
- In the above-described medicine dispensing device, the shutter may include a forward obstruction portion for obstructing the forward pipe line; and a buffer means provided at the forward obstruction portion and configured to buffer an impact caused by collision of the medicines proceeding within the forward pipe line.
- In case of providing the buffer means as described above, the impact caused by the collision between the shutter and the medicines transferred through the medicine transferring operation can be buffered. Thus, according to the above-described embodiment, the medicine dispensing device can surely prevent the medicines from breaking or chipping due to collision between the medicine and the shutter concomitantly with the medicine transferring operation.
- The above-described medicine dispensing device may include a partitioning means configured to partition an internal space of the main storage part. Further, the medicine dispensing device may be configured such that when the shutter becomes opened, both the exhaust pipe line and the forward pipe line become in communication with a space, which is formed according to a division caused by the partitioning means.
- According to such configuration, by partitioning the internal space of the main storage part through the partitioning means, the volume of the space, with which, when the shutter becomes opened, both the exhaust pipe line and the forward pipe line become in communication, can be decreased. Thus, although the suction and exhaust means does not have an excessively high exhaust capacity, the above-described medicine dispensing device can introduce the medicine transferred through the forward pipe line into the main storage part in the medicine introducing operation. Further, according to the above-described embodiment, the exhaust capacity of the suction and exhaust means can be minimized. Thus, when the medicines are introduced into the main storage part, it is possible to prevent the medicines from colliding into one another and to prevent occurrence of the breakage or chipping of the medicines.
- In the above-described medicine dispensing system, a velocity of the airflow flowing within the forward pipe line by operation of the airflow producing means may be slower than that of the exhaust concomitantly with operation of the suction and exhaust means.
- According to such configuration, it is possible to certainly prevent the medicine transferred from the sub unit through the medicine transferring operation from colliding with the shutter to thereby break.
- In the above-described medicine dispensing device, the exhaust pipe line may be connected to the sub storage part.
- The above-described medicine dispensing device may include a filter provided at a halfway portion of a flow line wherein an airflow is produced concomitantly with transferring the medicine between the sub storage part and the main storage part; an airflow amount detecting means configured to detect an airflow amount in the flow line concomitantly with transferring the medicine from the main storage part to the sub storage part; and a clogging judging means configured to judge a clogging of the filter based on the airflow amount detected by the airflow amount detecting means.
- According to such configuration, the clogging of the filter can be easily and certainly detected and thus maintenance of the filter can be performed at an appropriate timing.
- Further, it is preferred that the above-described medicine dispensing device is configured to transfer the medicine to the main storage part by increasing the output of the airflow producing means and/or the suction and exhaust means upon a condition of decrease in the airflow amount detected by the airflow amount detecting means, and to judge the clogging of the filter by the clogging detecting means upon a condition of increase in the output of the airflow producing means and/or the suction and exhaust means.
- Where the medicine dispensing system is configured as such, it is possible to avoid that the medicine under transfer is transferred to the main storage part and stays in the medicine transfer path by increasing the output of the airflow producing means or the suction and exhaust means prior to judging the clogging of the filter. Thus, according to such configuration, it is possible to prevent the troubles in the dispensing operation, which may occur because the medicine is completely transferred to the main storage part in the clogging of the filter.
- The above-described medicine dispensing device may include a filter provided at a halfway portion of a flow line wherein an airflow is produced concomitantly with transferring the medicine between the sub storage part and the main storage part; an airflow amount detecting means configured to detect an airflow amount in the flow line concomitantly with transferring the medicine from the main storage part to the sub storage part; and a notifying means. The medicine dispensing device may be configured to transfer the medicine to the main storage part by increasing the output of the airflow producing means and/or the suction and exhaust means upon a condition of decrease in the airflow amount detected by the airflow amount detecting means, and to notify the clogging of the filter by the notifying means.
- According to such configuration, when it is assumed that the filter is clogged due to a decrease in the airflow amount detected by the airflow amount detecting means, the medicine under the transferring operation is certainly transferred to the main storage part and at the same time, the clogging of the filter is immediately notified, thereby urging users to take suitable measures.
- Further, according to the medicine dispensing device one embodiment, the transfer device may include a forward pipe line in communication with the sub storage part and configured to be connected to the main storage part; an airflow producing means configured to produce an air flow within the forward pipe line from the sub unit toward the main unit; and a delivery part connected to the forward pipe line and configured to receive and dispense the medicine transferred from the sub unit through the forward pipe line at the main unit. The delivery part may include a delivery container, to which the forward pipe line is connected, and a shutter. The delivery container may include an internal space, which is configured such that the medicine transferred through the forward pipe line freely falls therein, and a dispensing opening disposed at a bottom thereof to dispense the medicine. The shutter may be configured to be changed between a dispensing-allowed state where the medicine is allowed to be dispensed from the dispensing opening, and a dispensing-unallowed state.
- In the medicine dispensing device of the present invention, the medicine dispensed from the sub storage part is transferred to the main storage part by having the shutter be in the dispensing-unallowed state where the medicine is not dispensed and by operating the airflow producing means. Thereby, the medicine transferred to the main unit is first received in the delivering part, and thereafter the medicine can be dispensed from the delivering part by converting the shutter. Thus, a medicine dispensing system may be constructed, wherein the medicine stored in the sub storage part can be dispensed in the main unit, by employing the medicine dispensing device as the sub unit and combining such a sub unit with the main unit.
- In the above-described medicine dispensing device, it is preferred that the delivery container may include an exhaust hole for exhausting an airflow flowing in through the forward pipe line and the exhaust hole may be positioned downwardly of a connection position between the delivery container and the forward pipe line.
- According to such configuration, the airflow flowing into the delivery container through the forward pipe line is allowed to flow downwardly. Also, the medicine introduced into the delivery container through the forward pipe line can drop smoothly along with the airflow.
- In the above-described medicine dispensing device, the delivery container may include a side portion (A) connected to the forward pipe line; and a pair of opposed side portions (B, C) crossing to the side portions. The exhaust hole may be provided at each of the pair of the side portions (B, C).
- Where the medicine dispensing device is configured as such, the airflow flowing into the delivery container through the forward pipe line is allowed to bifurcately flow to the exhaust holes provided at the side portions (B, C). Thus, the medicine can drop more smoothly within the delivery container.
- In the above-described medicine dispensing device, it is preferred that a buffer means configured to buffer an impact caused by the collision of the medicine may be provided within the delivery container. It is preferred that the forward pipe line may be connected to a side portion of the delivery container, and that the buffer means may be disposed opposite to the side portion to which the forward pipe line is connected.
- Where the medicine dispensing device is configured as such, when the medicine is introduced into the delivery container from the forward pipe line to the extent that it collides against the buffer means, the impact exerted to the medicine due to collision can be decreased and the medicine can be prevented from breaking or chipping.
- In the medicine dispensing device of some embodiments, the shutter may be configured to change an inclination thereof within an internal space of the delivery container. The shutter may become into the dispensing-unallowed state where the medicine is not dispensed from the dispensing opening when the shutter is situated to obliquely traverse the internal space of the delivery container. And, the shutter may become into the dispensing-allowed state where the medicine is dispensed from the dispensing opening by changing the inclination of the shutter from the dispensing-unallowed state.
- Where the medicine dispensing device is configured as such, since the shutter is inclined within the delivery container in the dispensing-unallowed state where the medicine is not dispensed from the dispensing opening, a dropping distance of the medicine within the delivery container can be shortened. Further, the medicine can be guided to the bottom side along the shutter. Thus, according to such configuration, the impact exerted on the medicine due to dropping of the medicine within the delivery container can be minimized.
- The delivery container, which the medicine dispensing device of the present invention employs, may be configured to be divided into two or more sub container bodies.
- Where the medicine dispensing device is configured as such, since the delivery container is divided into each sub container body, cleaning the inside of the delivery container and maintenance thereof can be easily performed.
- In the above-described medicine dispensing device, the delivery part may further include an outer container, in which the delivery container may be disposed. The delivery container may include an exhausting part for exhausting an airflow exhausted from the delivery container into the outer container outwardly of the outer container.
- According to such configuration, the airflow exhausted from the delivery part into the outer container can be exhausted through the exhausting part outwardly of the outer container. Thus, according to such configuration, the airflow produced concomitantly with transferring the medicine can be exhausted through the exhausting part. Also, it is possible to prevent dust from blowing under the influence caused by the exhausted airflow.
- In the above-described medicine dispensing device, the exhausting part may preferably include a primary filter; and a secondary filter disposed downstream of the primary filter in an exhaust flow direction, the secondary filter having meshes finer than the primary filter.
- According to such configuration, when the dust is contained in the airflow exhausted from the delivering part to the outer container, such dust can be prevented from leaking outwardly of the outer container. Further, as described above, the primary filter with sparse meshes is disposed upstream of the secondary filter with fine meshes in the exhaust flow direction, thereby enlarging a service life of the secondary filter with fine meshes.
- In the above-described medicine dispensing device, the delivery container and the forward pipe line may be connected to each other via a flexible joint pipe.
- According to such configuration, when some stress acts on the forward pipe line, such stress is absorbed or mitigated through the joint pipe constituting a joint portion between the delivering part and the forward pipe line, thereby preventing the joint portion between the delivering part and the forward pipe line from being broken.
- In the above-described medicine dispensing device, it is preferred that the shutter may go into the dispensing-allowed state and the airflow producing means may be operated until a transfer operation of a medicine from the sub unit to the main unit is completed and a next transfer operation is done thereafter, thereby performing a sweeping operation for sweeping a medicine transfer passage formed in the transfer device.
- According to such configuration, the medicine transfer passage formed in the transfer device can be maintained cleanly with ease.
- Further, in an alternate embodiment a medicine dispensing device is provided, which is configured to rapidly and reliably detect abnormality in packing paper sheet transfer in a packing paper sheet conveying part, and a medicine dispensing system including the same. Further, a medicine dispensing device and a medicine dispensing system is provided, which are configured to obtain a packed medicine at a desired position in a packing part.
- In one embodiment a medicine dispensing device includes a storage part configured to store and dispense a medicine; a packing part configured to pack the medicine dispensed from the storage part into a packing paper sheet; and a packing paper sheet conveying part configured to convey a packing paper sheet into which the medicine is packed by the packing part. The packing paper sheet conveying part includes a packing paper sheet conveying means configured to convey the packing paper sheet along a predetermined conveyance path through contact with the packing paper sheet; and a detecting means configured to contact the packing paper sheet passing through the transfer path and operate independently of the packing paper sheet conveying means. It is detected upon a condition of not operating of the detecting means during operation of the packing paper sheet conveying means whether abnormality in transferring a packing paper sheet occurs.
- The medicine dispensing device of the second present invention includes, at the packing paper sheet conveying part, the detecting means contacting the packing paper sheet and operating independently of the packing paper sheet conveying means. The medicine dispensing device can detect whether or not the packing paper sheet transfer is normal by the detecting means. Further, the medicine dispensing device of the present invention can rapidly and precisely detect an abnormality in the packing paper sheet transfer. Thus, the medicine dispensing device can perform appropriate measures such as stopping the packing paper sheet transfer, or stopping to dispense medicines to the packing paper sheet. It is possible to minimize the amount of the packing paper sheet or the medicine, which become unnecessary when there is an abnormality in the packing paper sheet transfer.
- Further, another embodiment is configured to rapidly and precisely perform an analysis to prevent the occurrence of wasted packing paper sheets, and a medicine dispensing system including the same.
- Further the detecting means may include a roller independently rotatable of the packing paper sheet conveying means; and a rotation detecting means configured to detect a rotation of the roller.
- According to such configuration, there can be provided a medicine dispensing device which can detect an abnormality in packing paper sheet transfer based on whether the rotation of the roller is detected by the rotation detecting means.
- Further, the packing paper sheet conveying part may be configured to bend the conveyance path of the packing paper sheet.
- According to such configuration, there can be provided a medicine dispensing device, which can remove the medicine packed in the packing part at a desired position by appropriately bending the conveyance path in the packing paper sheet conveying part.
- In the medicine dispensing device according to the above-described embodiment, in order to rapidly detect the abnormality in packing paper sheet transfer, an abnormality in packing paper sheet transfer can be detected in a position as far upstream as possible in a conveyance direction of the packing paper sheet where the occurrence of the abnormality in packing paper sheet transfer can be accurately detected. Specifically, the abnormality in packing paper sheet transfer can be detected in a position as far upstream as possible in the conveyance direction of the packing paper sheet where a conveyance force acts on the packing paper sheet.
- Thus, the detecting means may be situated upstream in the conveyance direction of the packing paper sheet in the packing paper sheet conveying means.
- According to such configuration, there can be provided a medicine dispensing device, which can rapidly and accurately grasp an abnormality in packing paper sheet transfer when it occurs.
- Further, the packing paper sheet conveying part may include a packing part for packing medicine. The packing paper sheet conveying means may be provided downstream in the conveyance direction of the packing paper sheet relative to the packing part. The packing paper sheet conveying means may include a receiving part receiving a packing paper sheet conveyed from the packing part; and a conveying part downstream of the conveying of the packing paper sheet received in the receiving part. The detecting means may be disposed near a boundary between the receiving part and the conveying part.
- In the medicine dispensing device, the receiving part receiving the packing paper sheet is provided in the packing paper sheet conveying means. In the conveying part, a conveyance force acts on the packing paper sheet received in the receiving part to convey the packing paper sheet. Thus, where the detecting means is disposed near the boundary between the receiving part and the conveying part, similar to the medicine dispensing device of the present invention, an abnormality in packing paper sheet transfer can be rapidly and accurately detected.
- Further, there is provided a medicine dispensing system including a main unit; one or more sub units; and a transfer device configured to connect the main unit and the sub units. The main unit includes the above-described medicine dispensing device. The sub unit includes a sub storage part configured to store and dispense a plurality kinds of medicines. The transfer device transfers the medicine dispensed from the sub storage part toward the main unit. The packing part of the main unit packs and dispenses the medicine.
- The medicine dispensing system may include the main unit and the sub unit. It is configured such that the medicine dispensed from the sub storage part provided in the sub unit is transferred to the main unit through the transfer device and is packed and dispensed together with the medicine dispensed in the main unit. However, when the packing paper sheet conveying part provided in the main unit cannot rapidly and accurately detect an abnormality in packing paper sheet transfer, the medicine dispensed in the main unit as well as the medicine dispensed in the sub unit are not allowed to be properly packed. As a result, when the medicines dispensed from both the main unit and the sub unit are allowed to be packed together as described in the medicine dispensing system of the present invention, not detecting the abnormality in packing paper sheet transfer rapidly and accurately raises problems in that the wasted amount of the packing paper sheet and the medicine becomes excessive.
- Thus, a medicine dispensing device in some embodiments may be employed as the main unit. Thus, when an abnormality in packing paper sheet transfer is detected in the main unit, such abnormality can be rapidyl and accurately detected. Further, an abnormality in packing paper sheet transfer can be detected rapidly and accurately in some embodiments, the medicine dispensing device can perform appropriate measures such as stopping the packing paper sheet transfer, or stopping to dispense medicines to the packing paper sheet in case of the occurrence of an abnormality in packing paper sheet transfer. Thus, the wasted amount of the packing paper sheet and the medicine can be minimized.
- There can be provided in other embodiments, a medicine dispensing device, which is configured to rapidly and reliably detect an abnormality in packing paper sheet transfer in a packing paper sheet conveying part, and the medicine dispensing system including the same. Further, there can be provided a medicine dispensing device and a medicine dispensing system, which are configured to remove a medicine packed in the packing part at a desired position.
- Next, another embodiment will be explained hereinafter. There exists in the art a medicine dispensing device as disclosed in the below-mentioned
reference Patent Document 3. A prior art medicine dispensing device has a medicine dispensing means. Such a prior art medicine dispensing device is configured to pack medicines dispensed from the medicine dispensing means according to prescriptions into a packing paper sheet at a packing means. Further, as disclosed inPatent Document 3, the prior art medicine dispensing device includes a printing means and is configured to print necessary information such as contents of the packed medicine on the packing paper sheet through the printing means. (see Patent Document 3: Japanese Laid-Open Patent Application No. 2006-130307). - In a packing work performed by the prior art medicine dispensing device disclosed in the
Patent Document 3, pharmacists monitor whether medicines to be fed to the packing part and to be packed therein are accurately packed. The prior art medicine dispensing device disclosed in thePatent Document 3 is configured to assume that the medicines to be packed are fed to the packing part at a time when the medicines to be fed to the packing part and to be packed therein are ready and then to perform a printing operation to a packing paper sheet through the printing means. Thus, in the packing work performed by the prior art medicine dispensing device disclosed in thePatent Document 3, it cannot be judged by looking over the information printed on the packing paper sheet whether the medicines to be packed are accurately packed. Thus, it has a problem in that the examination work becomes complicated. Further, it has another problem in that the packing paper sheet, to which the printing operation is performed after the medicines are already packed, appears to be under a normally packed state. Further, in the prior art medicine dispensing device, even if the medicines to be packed are not ready due to an abnormality in feeding medicines to the packing part, the printing operation is performed to a packing paper sheet, thereby wasting the packing paper sheet. - Thus, in one embodiment a medicine dispensing device, which is configured to rapidly and precisely perform an examination work and to prevent the occurrence of wasted packing paper sheets, and a medicine dispensing system including the same.
- In one embodiment a medicine dispensing device includes a medicine dispensing means configured to dispense medicine according to a prescription; a medicine preparing means configured to receive a medicine dispensed from the medicine dispensing means and to dispense the same at a predetermined time; a packing means configured to pack medicine dispensed from the medicine preparing means into a packing paper sheet; a packing paper sheet feeding means configured to feed a packing paper sheet to the packing means; and a printing means configured to print predetermined information on a packing paper sheet fed from the packing paper sheet feeding means to the packing means. The printing means is disposed upstream of the packing means in a flow direction of the packing paper sheet fed by the packing paper sheet feeding means. The length of the path, through which a packing paper sheet passes between the printing means and the packing means, is n times the length of a packing paper sheet necessary for packing medicine for a single pack. The medicine preparing means includes a plurality of sections configured to gather the medicine dispensed from the medicine dispensing means for one pack respectively and is configured to dispense the medicines gathered in the plurality of sections in predetermined order. The printing means prints information corresponding to a section A of the plurality of sections on the packing paper sheet at a timing earlier, by a time period necessary for dispensing a medicine for a section n from the medicine preparing means, than a timing of dispensing a medicine gathered in the section A.
- In another embodiment, the length of the path, through which the packing paper sheet passes between the printing means and the packing means, is set n times of the length of the packing paper sheet necessary for packing a medicine for one pack. Further, the medicine preparing means, which the medicine dispensing device of the present invention includes, includes a plurality of sections and is configured to dispense the medicine gathered in each of the sections in a predetermined order. Thus, in the medicine dispensing device of one embodiment, the medicine dispensed from the section A is packed into the packing paper sheet, which the printing means prints at a timing earlier, by a time period necessary for dispensing a medicine for the section n (i.e., equal to n packs) from the medicine preparing means toward the packing means, than a timing of dispensing a medicine gathered in the section A. That is, in the medicine dispensing device of this embodiment, a medicine to be packed is supplied to the section A at a timing prior to performing the print operation corresponding to the section A to the packing paper sheet. Further, a timing when the medicine gathered in the section A is dispensed to the packing part and a timing when a section of a packing paper sheet with the information corresponding to the section A printed thereon reaches the packing part coincide. Thus, the medicine dispensing device in some embodiments performs printing to a packing paper sheet upon a condition that a medicine to be packed is supplied to the section A. Further, it can easily monitor whether or not a medicine to be packed is exactly supplied and resolve the problem of wasted packing paper sheets resulting from abnormality in feeding a medicine.
- Further, in the above-described medicine dispensing device, a printing operation to the packing paper sheet may be performed by the printing means upon a condition that the medicine is fed into section A up to a time earlier by the time period necessary for dispensing a medicine for the section n from the medicine preparing means than the time of dispensing a medicine gathered in the section A of the plurality of sections in the medicine preparing means.
- Further, in the above-described medicine dispensing device, the medicine is dispensed from the medicine dispensing means to section A at a time earlier by a time period more than the time period necessary for dispensing a medicine for the section n from the medicine preparing means than the time of dispensing a medicine gathered in section A in the medicine preparing means. Thus, the information corresponding to section A is printed on the packing paper sheet after the medicine is fed into section A. Thus, the medicine dispensing device can easily monitor whether or not a medicine to be packed is accurately packed and resolve the waste of a packing paper sheet resulting from an abnormality in feeding a medicine.
- Further a medicine dispensing device includes a medicine dispensing means configured to dispense a medicine according to a prescription; a medicine preparing means configured to receive a medicine dispensed from the medicine dispensing means and to dispense the same at a predetermined time; a packing means configured to pack a medicine dispensed from the medicine preparing means into a packing paper sheet; a packing paper sheet feeding means configured to feed a packing paper sheet to the packing means; and a printing means configured to print predetermined information on a packing paper sheet fed from the packing paper sheet feeding means to the packing means. The printing means is disposed upstream of the packing means in a flow direction of the packing paper sheet fed by the packing paper sheet feeding means. The medicine preparing means includes a plurality of sections configured to gather the medicine for one pack dispensed from the medicine dispensing means respectively. The medicine preparing means is configured to dispense the medicines gathered in the plurality of sections in a predetermined order. A medicine is dispensed from the medicine dispensing means into one section A of the plurality of sections at a time earlier by a timing Z as early as a time period Y when the packing paper sheet fed by the packing paper sheet feeding means moves from a position corresponding to the printing means to the packing means, than a timing X when the medicine in the section A is dispensed from the medicine dispensing means toward the packing means. Information corresponding to section A is printed on the packing paper sheet at the time Z by the printing means.
- In the above-described medicine dispensing device, medicine is fed into section A of the medicine preparing means at a time earlier than the time Z. Further, the information corresponding to section A is printed on the packing paper sheet by the printing means at the time Z as early as the time period Y when the packing paper sheet fed by the packing paper sheet feeding means moves from the position corresponding to the printing means to the packing means, from the timing X when the medicine in section A is dispensed from the medicine dispensing means toward the packing means. That is, the information corresponding to section A is printed on a portion of the packing paper sheet, which is used for packing the medicine in section A, at the same time as, or later than a time for feeding the medicine into section A. Thus, the medicine dispensing device can perform the printing operation to the medicine dispensing device after ascertaining that the medicine to be packed is exactly fed into the section. Further, the medicine dispensing device can easily monitor whether or not the medicine to be packed is exactly fed and resolve the waste of a packing paper sheet resulting from an abnormality in feeding a medicine.
- Further, the printing operation to the packing paper sheet may be performed upon a condition that the medicine is fed into section A at a time earlier than the time Z.
- With such configuration, if the printing operation to the packing paper sheet is not performed, it can be judged that the medicine is not fed exactly before the time Z. Thus, examining whether or not the medicine is exactly packed can become easy. Further, according to such configuration, if the medicine is not fed into the section A before the time Z, the printing operation to the packing paper sheet stops, thereby preventing the occurrence of the wasted packing paper sheet in advance.
- Further, a print purporting that the medicine to be packed runs short may be made on the packing paper sheet by the printing means upon a condition that the medicine to be packed is not inputted to section A until the time earlier than the time Z.
- According to such configuration, it is ascertained through only looking over the print made on the packing paper sheet that the medicine to be packed runs short. Thus, the examination work can be performed more easily and reliably.
- Further, in the above-described medicine dispensing device, the medicine preparing means may include a section forming body having a plurality of sections arranged circumferentially; and a dispensing opening. The section forming body may be configured to move relative to the dispensing opening. When the section reaches a position corresponding to the dispensing opening, the medicine gathered in the section may be disposed through the dispensing opening.
- Further, a medicine dispensing device comprises: a medicine dispensing means configured to dispense a medicine according to a prescription; a medicine preparing means configured to receive a medicine dispensed from the medicine dispensing means and to dispense the same at a predetermined time; a packing means configured to pack a medicine dispensed from the medicine preparing means into a packing paper sheet; a packing paper sheet feeding means configured to feed a packing paper sheet to the packing means; and a printing means configured to print a predetermined information on a packing paper sheet fed from the packing paper sheet feeding means to the packing means. The printing means is disposed upstream of the packing means in a flow direction of the packing paper sheet fed by the packing paper sheet feeding means. The medicine preparing means comprises: a rotatable section forming body; an opening for dispensing a medicine from the medicine preparing means; and a hole to which the medicine dispensed from the medicine dispensing means is inputted. The section forming body includes a plurality of sections in a circumferential direction. The section is configured to gather a medicine for one pack. When the section forming body rotates and each of the sections reaches a position corresponding to the hole, the medicine is inputted to the section through the hole. When the section forming body rotates and each of the sections reaches a position corresponding to the opening, the medicine in the section is dispensed. The hole is formed in a position upstream of the opening in a rotating direction of the section forming body.
- In the above-described medicine dispensing device, a length of a path, through which a packing paper sheet passes between the printing means and the packing means, is n times of a length of a packing paper sheet necessary for packing a medicine for one pack. The hole is formed in a position upstream of the opening by more than n sections in the rotating direction of the section forming body.
- Further, the medicine dispensing means capable of dispensing a medicine according to a prescription includes: a main storage part; a manual distributing unit; a collecting hopper for feeding a medicine dispensed from the main storage part; and a manual distributing hopper for feeding a medicine dispensed from the manual distributing unit. The hole to which the medicine dispensed from the medicine dispensing means is inputted comprises: a hole for connection to the collecting hopper and a hole for connection to the manual distributing hopper. The hole for connection to the collecting hopper and the hole for connection to the manual distributing hopper are apart from each other in the circumferential direction. The hole for connection to the collecting hopper and the hole for connection to the manual distributing hopper are formed in a position upstream of the opening for dispensing a medicine from the medicine preparing means by more than n sections in the rotating direction of the section forming body.
- Further, the medicine preparing means comprises: a shutter provided in each of the sections of the medicine preparing means; a dispensing opening for dispensing a medicine from the medicine dispensing means; and a contactor provided near the opening. When each of the sections reaches a position corresponding to the dispensing opening, the shutter provided in each of the sections is pressed by contact to the contactor and then opened, thereby dispensing the medicine in each of the sections.
- Further, the above-described medicine dispensing device further comprises a medicine standby part provided between the medicine preparing means and the medicine dispensing means. The medicine standby part includes: a funnel-shaped standby hopper; a movable lid; and a lid moving mechanism. The movable lid moves upward and downward by an operation of the lid moving mechanism to open and close a discharging opening formed in the standby hopper.
- Further, there is provided a medicine dispensing system that includes a main unit; one or more sub units; and a transfer device configured to connect the main unit and the sub units. The main unit includes the above-described medicine dispensing device. The sub unit includes a sub storage part configured to store and dispense a plurality kinds of medicines. The transfer device transfers the medicine dispensed from the sub storage part toward the main unit and feeds the medicine into the section provided in the medicine preparing means. The packing means of the main unit packs and dispenses the medicine.
- The medicine dispensing system includes the main unit and the sub unit. It is configured such that the medicine dispensed in the sub unit is transferred to the medicine preparing means provided in the main unit and is packed and dispensed together with the medicine dispensed in the main unit by the packing means. However, in the medicine dispensing system, there is a possibility that an abnormality in dispensing medicine to the medicine preparing means occurs in the main unit. In addition, there is another possibility that an abnormality in dispensing medicine occurs in the sub unit, and that troubles take place during transferring a medicine to the medicine preparing means through the transfer device. As such, where the main unit is provided, the medicine dispensing system may have many factors associated with the abnormality in dispensing medicine to the medicine preparing means. Accordingly, similar to the above-described medicine dispensing device of the present invention, it is preferred that the above-described medicine dispensing system may have some means so that it can easily monitor whether a packing operation is accurately performed and prevent the packing paper sheet from wasting concomitantly with the abnormality in dispensing a medicine to the medicine preparing means.
- Thus, the medicine dispensing system, which is provided based on such knowledge, employs the above-described medicine dispensing device as the main unit. Thus, the medicine dispensing system can prevent the packing paper sheet from being wasting in conjunction with an abnormality in dispensing a medicine to the medicine preparing means.
- According to another embodiment, there can be provided a medicine dispensing device, which is configured to easily and accurately perform the examination work regarding whether or not packing medicine is accurately performed and to prevent the packing paper sheet from wasting even if the medicine to be dispensed becomes unready due to an abnormality in feeding a medicine to the packing part. Further, there can be provided a medicine dispensing system that includes such a medicine dispensing device.
- Further, in the above-described medicine dispensing system, the medicine preparing means of the main unit includes: a rotatable section forming body; an opening for dispensing a medicine from the medicine preparing means; and a hole to which the medicine dispensed from the medicine dispensing means is inputted. The section forming body includes a plurality of sections in a circumferential direction, the section being configured to gather a medicine for one pack. When the section forming body rotates and each of the sections reaches a position corresponding to the hole, the medicine is inputted to the section through the hole. When the section forming body rotates and each of the sections reaches a position corresponding to the opening, the medicine in the section is dispensed. The main unit has a main storage part and a manual distributing unit as the medicine dispensing means configured to dispense a medicine according to a prescription and the main unit comprises a collecting hopper for feeding a medicine dispensed from the main storage part and a sub collecting hopper for feeding a medicine dispensed from the sub storage part. The medicine preparing means comprises a hole for connection to the collecting hopper and a hole for connection to the sub collecting hopper at a position corresponding to each of the sections of the section forming body, the hole for connection to the collecting hopper and the hole for connection to the sub collecting hopper being apart from each other in the circumferential direction. The medicines fed by the collecting hopper and the sub collecting hopper are inputted to each of the sections through the holes. The hole for connection to the collecting hopper and the hole for connection to the sub collecting hopper are formed in a position upstream of the opening for dispensing a medicine from the medicine preparing means in the rotating direction of the section forming body.
- Further, a length of a path, through which a packing paper sheet passes between the printing means and the packing means provided in the main unit, is n times of a length of a packing paper sheet necessary for packing a medicine for one pack. The hole is formed in a position upstream of the opening by more than n sections in the rotating direction of the section forming body.
- Next, another embodiment will be explained hereinafter. There exists in the art a medicine dispensing device as disclosed in the below-mentioned
reference Patent Document 4. A prior art medicine dispensing device includes a plurality of medicine feeding containers configured to store medicine in a storage part and dispense the medicine. Such a prior art medicine dispensing device is configured to dispense the medicine from each of the medicine feeding container by the amount corresponding to a prescription and pack the same. (see Patent Document 4: Japanese Laid-Open Patent Application No. 2001-276183). - The prior art medicine dispensing device is used in such a manner that each of the medicine feeding containers accommodates different kinds of medicines. However, the prior art medicine dispensing device is not configured to simply and accurately grasp characteristic data of each medicine feeding container, such as a date and time when the medicine feeding container is filled with medicines, a user filling the medicine feeding container, data related to medicines accommodated in the medicine feeding container, etc. Further, as the number of the medicine feeding containers increases with an increase in the kinds of medicines to be dealt with, such a tendency becomes strong. Thus, the relevant art requires a medicine dispensing device configured to simply and accurately grasp characteristic data of each medicine feeding container. Similarly, a medicine dispensing system, which is constructed by combining a plurality of medicine dispensing devices, is required to be configured to simply and accurately grasp characteristic data of each medicine feeding container.
- Thus, to satisfy the aforementioned demand, it is an object of the present invention to provide a medicine dispensing device and a medicine dispensing system, which are configured to simply and accurately grasp characteristic data of each medicine feeding container.
- In order to accomplish the above objects, there is provided a medicine dispensing device, which includes a medicine feeding container configured to store a medicine, the medicine feeding container including an information recordable medium; a container mounting part configured to mount the medicine feeding container; and a control means. The medicine is allowed to be dispensed by mounting the medicine feeding container to the container mounting part. The control means is configured to perform a data communication for a characteristic data of the medicine feeding container with the information recordable medium of the medicine feeding container.
- According to such configuration, there is provided the medicine dispensing device, which can perform the data communication for the characteristic data between the control means and the medicine feeding container having the information recordable medium and can simply and accurately grasp the characteristic data.
- Further, a medicine dispensing device, which is provided based on the same knowledge, may include a storage means configured to store and dispense medicine; and a control means configured to data-communicate with an information recordable medium. The storage means may include a plurality of attachable/detachable medicine feeding containers configured to store and dispense the medicine. The information recordable medium may be provided in some or all of the medicine feeding containers. A data communication for the characteristic data of the medicine feeding container may be performed between the information recordable medium of the medicine feeding container and the control means.
- The above-described medicine dispensing device includes a storage means configured to store and dispense medicine; and a control means configured to data-communicate with the information recordable medium. Herein, the storage means includes a shelf or drum, in which a plurality of medicine feeding container are removably provided (for example, this may be referred to as a main storage part or a sub storage part in embodiments described below). Further, in the medicine dispensing device, a plurality of medicine feeding containers configured to store and dispense a medicine are removably provided in the storage means, which includes a shelf or drum. Herein, the medicine feeding container corresponds to a feeder container in the below-described embodiments and a container capable of dispensing the medicine accommodated therein. The above-described storage means, which includes the medicine feeding container, can dispense the medicine dispensed from the medicine feeding container for the purpose of packing the same.
- With the above-described constitution, there can be provided a medicine dispensing device, which can data communicate with the control means with respect to the characteristic data of each of the medicine feeding containers with the information recordable medium and thus can simply and accurately grasp the characteristic data.
- Further, the control means may be configured to data communicate with an operator information recordable medium recording an operator information specifying an operator. The operator information read from the operator information recordable medium through the data communication may be recorded into the information recordable medium.
- According to such constitution, information on an operator, who performs tasks relevant to the medicine feeding container, such as filling the medicine feeding container with medicines, may be recorded into the information recordable medium of each of the medicine feeding containers.
- Further, the medicine dispensing device may be configured to operate in a plurality of operation modes. The operation mode may change in a predetermined operation mode selected from a plurality of operation modes upon a condition that the data communication is allowed between the control means and the information recordable medium of the medicine feeding container removed from a container mounting part.
- In the medicine dispensing device, the operation mode changes upon a condition that the data communication is allowed between the control means and the information recordable medium of the medicine feeding container. That is, it can be used as a trigger for changing the operation modes that the information recordable medium provided in each of medicine feeding container is allowed to data communicate with the control means. Thus, efforts required to change the operation modes can be minimized and misoperation can be prevented.
- Further, the medicine dispensing device may include a mark reading means for reading an identification mark assigned to each of the kinds of medicine. The kinds of medicine may be specified by the control means based on the identification mark read by the mark reading means. Information on the kinds of medicine may be recorded into the information recordable medium through data communication between the control means and the information recordable medium of the medicine feeding container removed from the container mounting part.
- According to such configuration, if the mark reading means reads the identification mark assigned to each of the kinds of medicine when filling the medicine feeding container removed from the container mounting part with a medicine, the information on the kind of such a medicine can be recorded into the information recordable medium of the medicine feeding container through data communication. Thus, according to the medicine dispensing device of one embodiment, when the medicine feeding container is filled with a medicine, the information on the kinds of medicine can be easily and reliably recorded into the information recordable medium.
- The medicine dispensing device according to this embodiment may further include a cassette placing part configured to place the medicine feeding container removed from the container mounting part; and an interface means wiredly or wirelessly connected to the control means. When the medicine feeding container is placed on the cassette placing part, the data communication between the information recordable medium of the medicine feeding container and the control means may be allowed via the interface means.
- According to such configuration, efforts required to enable the data communication between the information recordable medium and the control means after removing the medicine feeding container from the container mounting part can be minimally saved.
- Further, the medicine dispensing device may further include an interface means wiredly or wirelessly connected to the control means. The interface means may be configured to read and record data as not in contact with the information recordable medium.
- According to such configuration, efforts required to enable the data communication between the information recordable medium and the control means after removing the medicine feeding container from the container mounting part can be saved.
- The above-described medicine dispensing device can data-communicate with the information recordable medium of each of the medicine feeding containers with respect to the characteristic data of the medicine feeding container. Thus, the medicine dispensing device can be configured to dispense medicines for purposes of packing the same even if the medicine feeding container accommodating a predetermined medicine is situated at any location in the storage means. However, some medicine of the plurality kinds of medicines is prone to bound, roll over, break or chip due to drop impact at a dispensing portion while dispensed from the medicine feeding container. In case of dealing with such a medicine, it must be dealt with in a different manner from those for other medicines (for example, adjustment in dispensing timing regarding bound or roll, means for mitigating drop impact, etc.) so as not to cause an abnormality in dispensing medicine. Accordingly, the medicine feeding container accommodating medicine having such a particular characteristics is attached to a location capable of resolving the foregoing matter.
- Further, medicines may be sequentially dispensed based on prescription data inputted to the control means and a plurality of the container mounting parts configured to mount the medicine feeding container may be provided. The control means may include: a correspondence relationship storing part regulating and storing a correspondence relationship between the plurality of the container mounting parts and the medicine feeding container to be attached to the plurality of container mounting parts; and a judging part. The judging part may be configured to perform an error judgment operation for judging the following states, by comparing the correspondence relation storing part and the characteristic data of the medicine feeding container obtained from the data communication with the information recordable medium of the medicine feeding container mounted on the container mounting part: a right mount state where the medicine feeding container is properly mounted on the container mount part coinciding with the correspondence relationship regulated in the correspondence relationship storing part; and a erroneous mount state where the medicine feeding container is erroneously mounted on the container mounting part against the correspondence relationship regulated in the correspondence relationship storing part. Dispensing the medicines may continue from other medicine feeding containers excluding an erroneously-mounted medicine feeding container upon a condition that it is judged by the error judgment operation that there is the erroneously mounted medicine feeding container, and that a medicine accommodated in the erroneously mounted medicine feeding container is not a medicine to be dispensed according to the prescription data. Dispensing the medicines may stop upon a condition that it is judged by the error judgment operation that there is the erroneously mounted medicine feeding container, and that a medicine accommodated in the erroneously mounted medicine feeding container is a medicine to be dispensed according to the prescription data.
- In the medicine dispensing device configured as such, the judging part of the control means performs the error judgment operation. Based on the correspondence relationship between the container mounting part and the medicine feeding container, which is regulated in the correspondence relationship storing part, it can be judged whether the medicine feeding container is properly mounted or erroneously mounted on the container mounting part dedicated for said medicine feeding container. Further, in the medicine dispensing device of the present invention, where the medicine feeding container is erroneously mounted and such a medicine feeding container does not accommodate a medicine to be dispensed, even if dispensing a medicine does not stop in other medicine feeding containers, problems such as bound, roll, breakage, chipping, etc. of medicines do not occur. And, stopping to dispense a medicine leads to loss of work efficiency. Accordingly, in the medicine dispensing device of some embodiments, where the erroneously mounted medicine feeding container does not accommodate a medicine to be dispensed, dispensing a medicine continues and the erroneously mounted medicine feeding container can be dismounted without stopping to dispense a medicine. Accordingly, even if the erroneously mounted medicine feeding container exists, the loss of work efficiency resulting therefrom can be minimized.
- By contrast, where the erroneously mounted medicine feeding container exists and such a medicine feeding container accommodates a medicine to be dispensed, continuing to dispense a medicine causes the aforementioned problems such as bound, roll, breakage, chipping, etc. of medicines. Accordingly, in such a case, the medicine dispensing device of in some embodiments is configured to stop to dispense a medicine. Thus, according to the medicine dispensing device in some embodiments, it is possible to prevent medicines from being dispensed from the erroneously mounted medicine feeding container.
- Further, it is preferred that medicines prone to bound, roll over, break or chip due to drop impact at the dispensing portion are dispensed at a side as low as possible.
- Thus, in the above-described medicine dispensing device provided based on such knowledge, the storage means may include a plurality of the container mounting parts configured to mount the medicine feeding container. The container mounting parts may be vertically arranged. It may be judged through the error judgment operation whether a medicine feeding container to be mounted on a container mounting part provided below a predetermined height is erroneously mounted on a container mounting part provided in a position above the predetermined height.
- According to such configuration, it can be prevented that the medicine feeding container accommodating the medicine to be dispensed at a side as low as possible (i.e. the aforementioned medicine causing problems such as bound, roll, breakage or chipping concomitantly with drop) is erroneously mounted on the container mounting part situated in a position above the predetermined height.
- Further, the above-described medicine dispensing device provided based on the same knowledge, the container mounting part configured to mount the medicine feeding container may be disposed in each of a plurality of container mounting regions defined along a height direction. The correspondence relationship storing part may regulate the correspondence relationship between the container mounting part and the medicine feeding container to be attached to the container mounting part as a relationship relative to the container mounting region located at a height corresponding to an upper attachment limit of a medicine feeding container that is determined according to a kind of medicine. The erroneous mount state may be judged through the error judgment operation when a medicine feeding container is mounted on a container mounting part of a container mounting region locating beyond a container mounting region located at a height corresponding to the upper attachment limit. The right mount state may be judged through the error judgment operation when a medicine feeding container is mounted on a container mounting part of a container mounting region located at a height below the upper attachment limit.
- In the medicine dispensing device, the correspondence relationship storing part can regulate the correspondence relationship between the container mounting regions and the height corresponding to the upper attachment limit of the medicine feeding container at a plurality of steps in view of that bound, roll, breakage or chipping occurs at what level concomitantly with drop. Further, the erroneous mount state can be judged through the error judgment operation based on such a regulation, when a medicine feeding container is mounted on a container mounting part of a container mounting region located upward beyond a container mounting region located at a height corresponding to the upper attachment limit. Thus, it is possible to prevent the occurrence of trouble such as an abnormality in dispensing a medicine resulting from the erroneous mount state.
- Further, the control means may be configured to perform a search operation for searching and selecting a container mounting part, on which the medicine feeding container judged to be in the erroneous mount state through the error judgment operation must be mounted.
- According to such configuration, it can be easily determined through the search operation on which container mounting part the erroneously mounted medicine feeding container must be mounted.
- Further, a search condition may be determined based on the characteristic data of the medicine feeding container obtained by the data communication with the information recordable medium, which the medicine feeding container judged to be in the erroneous mount state through the error judgment operation includes.
- According to such configuration, even if an operator does not separately input a search condition in the search operation, the container mounting part on which the erroneously mounted medicine feeding container must be mounted can be selected. Thus, convenience in the search operation can be enhanced.
- In the above-described invention, the storage means may be configured to move each of the container mounting parts to an attachment/detachment work position where an attachment/detachment work of the medicine feeding container can be performed. The container mounting part selected through the search operation may be moved to the attachment/detachment work position.
- In such a medicine dispensing device, a container mounting part located at a proper position, in which the erroneously mounted medicine feeding container must be properly attached, is moved to the attachment/detachment work position. Thus, convenience in attaching the medicine feeding container in the proper position can be enhanced.
- Further, there is provided a medicine dispensing system that includes a main unit; one or more sub units; and a transfer device configured to connect the main unit and the sub units. The main unit includes the above-described medicine dispensing device. The sub unit includes a sub storage means configured to store and dispense a plurality kinds of medicines. The sub storage means includes a plurality of attachable/detachable medicine feeding containers configured to store and dispense a medicine. The transfer device transfers the medicine dispensed from the sub storage means toward the main unit. The medicine is dispensed in the main unit.
- Such a medicine dispensing system includes the main unit and the sub unit. A plurality of medicine feeding containers are removably attached to both the storage means of the main unit and the sub storage means of the sub unit. Accordingly, the medicine dispensing system has a large number of medicine feeding containers and thus needs to be configured to even more easily and reliably control the characteristic data of each of the medicine feeding containers. Thus, the medicine dispensing system, which is provided based on such knowledge, includes the above-described medicine dispensing device as the main unit. As a result, the medicine dispensing system can simply and accurately grasp and control the characteristic data through the data communication between the control means provided in the main unit and the information recordable medium of each of the medicine feeding containers provided in the main unit and the sub unit.
- Thus, there can be provided a medicine dispensing device and a medicine dispensing system, which are configured to simply and accurately grasp the characteristic data of each medicine feeding container.
- According to another embodiment there can be provided a medicine dispensing system, which is configured such that a medicine dispensing device that includes a sub unit having a function of dispensing medicines is connected to a medicine dispensing device that includes a main unit having a function of packing medicines. Further, there can be provided a medicine dispensing device that can be appropriately employed to such a medicine dispensing system.
- Also, according to other embodiments, there can be provided a medicine dispensing device, which is configured to rapidly and reliably detect abnormality in packing paper sheet transfer in a packing paper sheet conveying part, and a medicine dispensing system including the same. Further, there can be provided a medicine dispensing device and a medicine dispensing system, which are configured to remove a packed medicine at a desired position in a packing part.
- Further, there can be provided a medicine dispensing device, which is configured to rapidly and precisely perform an examination work regarding whether or not packing a medicine is accurately performed and to prevent occurrence of a wasted packing paper sheet even if a medicine to be dispensed becomes unready due to abnormality in feeding a medicine to a packing part. Further, there can be provided a medicine dispensing system comprising such a medicine dispensing device.
- Furthermore, there can be provided a medicine dispensing device and a medicine dispensing system, which are configured to simply and accurately grasp a characteristic data of each medicine feeding container.
-
FIG. 1 is a perspective view showing a medicine dispensing system according to one embodiment of the present invention. -
FIG. 2 is a front view schematically showing the internal structure of the medicine dispensing system shown inFIG. 1 . -
FIG. 3 is a perspective view showing a structure near a main storage part of a main unit. -
FIG. 4( a) is a partially enlarged perspective view showing a structure of a drum.FIG. 4( b) is a sectional view showing that a cassette is attached to the drum.FIG. 4( c) illustrates a positional relationship between a main storage part and an irregular set detecting means. -
FIG. 5 is an exploded perspective view of a cassette. -
FIG. 6 is an exploded perspective view of a feeder container. -
FIG. 7 is a perspective view showing a medicine awaiting mechanism part. -
FIG. 8 is a perspective view showing a mechanism part. -
FIGS. 9( a) to 9(d) are side views sequentially showing a vertical movement of a slide shaft. -
FIG. 10( a) is a sectional view showing that a discharging opening of the medicine awaiting mechanism part is closed.FIG. 10( b) is a sectional view showing that the discharging opening is open. -
FIG. 11 is an exploded perspective view showing a medicine preparing part. -
FIG. 12 is a top plan view showing the internal structure of the medicine preparing part. -
FIGS. 13( a) to 13(f) are sectional views sequentially showing operating processes of a shutter provided in a section forming body. -
FIG. 14 is a perspective view showing structure near a medicine preparing part and a medicine packing part of the main unit. -
FIGS. 15( a) to 15(f) schematically illustrates that medicines are fed into the section forming body. -
FIG. 16 is a sectional view showing arrangement of a conveying means in the main unit. -
FIG. 17 is a perspective view showing the conveying means. -
FIG. 18( a) is a sectional view showing that an abnormality detecting mechanism is attached to a transfer means.FIG. 18( b) is a section view taken along the ling A-A inFIG. 18( a).FIG. 18( c) is a view viewed along an arrow B inFIG. 18( a). -
FIG. 19( a) is a rear view of the conveying means.FIG. 19( b) is a front view of the conveying means. -
FIG. 20( a) is a perspective view showing a work table.FIG. 20( b) is a block diagram showing the features of a data management system. -
FIG. 21( a) is a perspective view showing a transfer device viewed from a medicine dispensing part.FIG. 21( b) is a perspective view showing the transfer device viewed from a medicine receiving part. -
FIG. 22A is a front view showing an interface for calling a cassette.FIG. 22B is a front view showing an interface for calling a medicine name.FIGS. 22C and 22D are front views showing an interface for displaying a characteristic information of a container. -
FIG. 23 is a sectional view showing the medicine dispensing part of the transfer device shown inFIG. 21 .FIG. 23( a) is a sectional view showing transferring a medicine.FIG. 23( b) is a sectional view showing dispensing a medicine. -
FIG. 24 is a perspective view showing a counter device. -
FIG. 25 is a perspective view showing a variation of the transfer device.FIG. 25( a) is a perspective view showing that a medicine delivering unit of a transfer device according to a variation is expanded.FIG. 25( b) is a perspective view showing that the medicine delivering unit is contracted. -
FIG. 26 is an upper perspective view of the medicine delivering unit of the transfer device shown inFIG. 25 . -
FIG. 27 is a lower perspective view of the medicine delivering unit of the transfer device shown inFIG. 25 . -
FIG. 28 is a section view of the medicine delivering unit of the transfer device shown inFIG. 25 . -
FIG. 29( a) is an upper perspective view of a sliding base of the medicine delivering unit of the transfer device shown inFIG. 25 .FIG. 29( b) is a lower perspective view of the sliding base. -
FIG. 30( a) is an upper perspective view of a first sliding body of the medicine delivering unit of the transfer device shown inFIG. 25 .FIG. 30( b) is a lower perspective view of the first sliding body. -
FIG. 31( a) is an upper perspective view of a second sliding body of the medicine delivering unit of the transfer device shown inFIG. 25 .FIG. 31( b) is a lower perspective view of the second sliding body. -
FIG. 32 is a front view showing a further variation of a transfer device. -
FIG. 33 is a section view taken along the ling A-A inFIG. 32 . -
FIG. 34 is a front view showing one motion of the transfer device shown inFIG. 32 . -
FIG. 35 is a front view showing the other motion of the transfer device shown inFIG. 32 . -
FIG. 36 is a front view schematically showing major parts of the internal structure of a medicine dispensing system including a transfer device according to another variation. -
FIG. 37 is a perspective view showing the features of a medicine dispensing part employed in the transfer device shown inFIG. 36 .FIG. 37( a) illustrates that an area A of a shutter is located in the medicine dispensing part.FIG. 37( b) illustrates that an area B of the shutter is not located in the medicine dispensing part. -
FIG. 38 is a sectional view taken along the line X-X inFIG. 37( a). -
FIG. 39 is a perspective view showing the shutter provided in the medicine dispensing part shown inFIG. 37 . -
FIG. 40( a) is a view taken along an arrow X inFIG. 39 .FIG. 40( b) is a view taken along an arrow Y inFIG. 39 . -
FIG. 41 is a front view showing a variation of the medicine dispensing system shown inFIG. 36 . -
FIG. 42 is a perspective view showing yet another variation of a transfer device. -
FIG. 43 schematically shows features of a transfer device shown inFIG. 42 . -
FIG. 44 is an enlarged perspective view of a medicine dispensing part of the transfer device shown inFIG. 42 with a lid of an outer container removed therefrom. -
FIG. 45 is a top plan view of the medicine dispensing part of the transfer device shown inFIG. 42 with the lid of the outer container removed therefrom. -
FIG. 46 is a sectional view showing the structure of the medicine dispensing part of the transfer device shown inFIG. 42 with a side portion of a delivery container cut away. -
FIG. 47 is a sectional view showing the structure of the medicine dispensing part of the transfer device shown inFIG. 42 with a top portion of the delivery container cut away. -
FIG. 48 is a sectional view showing a medicine receiving part of the transfer device shown inFIG. 42 . -
FIG. 49 is a perspective view showing the structure near a manual distributing unit in a main unit of a medicine dispensing system according to one embodiment of the present invention. -
FIG. 50 is a side view showing the structure near the manual distributing unit in the main unit of the medicine dispensing system according to one embodiment of the present invention. -
FIG. 51 is a perspective view schematically showing features of a main storage part and a sub storage part. -
FIG. 52 is a block diagram showing a variation of a control means. -
FIG. 53 is a flow chat showing an error judgment operation of a medicine dispensing system. -
FIG. 54 is a flow chart showing operations of the medicine dispensing system. -
FIG. 55 is a front view showing a display of a manipulating panel when a feeder container insertion error occurs. -
FIG. 56 is a front view showing a display of the manipulating panel when a message for urging erroneous mount solution is emitted. -
FIG. 57 is a front view showing a display of the manipulating panel when a feeder container mount error occurs. -
FIG. 58 is a front view showing a display of a manipulating panel when a feeder container identification error occurs. -
FIG. 59 is a front view showing a display of a manipulating panel when a search condition is set. -
-
- 1 . . . Medicine Dispensing System
- 2 . . . Main Unit (Medicine Dispensing Device)
- 3 . . . Sub Unit (Medicine Dispensing Device)
- 5 . . . Transfer Device
- 20 . . . Main Storage Part
- 120 . . . Sub Storage Part
- 140 . . . Pipe Line
- 141 . . . Suction means (Transfer Means)
- 210 . . . Transfer Device
- 231 . . . Medicine Delivering Unit (Medicine Delivering Part)
- 234 . . . Turning Shaft
- 300 . . . Transfer Device
- 312 . . . Drive Unit (Direction Adjusting Means)
- 330 . . . Turning Part (Conveying Part)
- 340 . . . Medicine Container (Medicine Delivery container)
- 400 . . . Transfer Device
- 401 . . . Medicine Receiving Part (Sub Storage Part)
- 402 . . . Medicine Dispensing Part (Main Storage Part)
- 403 . . . Forward Pipe Line
- 405 . . . Blower (Airflow Producing Means)
- 408 . . . Pump (Suction and exhaust means)
- 410 . . . Exhaust Pipe Line
- 420 . . . Shutter
- 423 . . . Inclined Surface (Partitioning means)
- 440 . . . Filter
- 441 . . . Buffer (Buffer Means)
- 442 . . . Forward Isolation Portion
- 500 . . . Transfer Device
- 502 . . . Forward Pipe Line
- 504 . . . Blower (Airflow Producing Means)
- 510 . . . Medicine Dispensing Part (Delivering Part)
- 512 . . . Delivery container
- 512 a . . . Side Portion (Side Portion A)
- 512 b . . . Side Portion (Side Portion B)
- 512 c . . . Side Portion (Side Portion C)
- 514 . . . Shutter
- 516 . . . Internal Space
- 518 . . . Bottom Portion
- 520 . . . Dispensing Opening
- 522 . . . Buffer Means
- 524 . . . Upper Sub Container Body (Sub Container Body)
- 524 p . . . Exhaust Hole
- 526 . . . Lower Sub Container Body (Sub Container Body)
- 526 p . . . Exhaust Hole
- 530 . . . Outer Container
- 532 . . . Exhaust Part
- 534 . . . Primary Filter
- 536 . . . Secondary Filter
- 540 . . . Joint Pipe
- A
medicine dispensing system 1, a main unit (medicine dispensing device) 2 and a sub unit (medicine dispensing device) 3 according to one embodiment of the present invention will be described in detail with reference to the accompanying drawings. As shown inFIG. 1 , themedicine dispensing system 1 has themain unit 2 and thesub unit 3. Themain unit 2 forms a basic section of themedicine dispensing system 1. Further, thesub unit 3 may be used in combination with themain unit 2. Themedicine dispensing system 1 has atransfer device 5 operated between themain unit 2 and thesub unit 3. In themedicine dispensing system 1 according to the present embodiment, thetransfer device 5 is disposed in thesub unit 3. The transfer device is configured to transfer the medicine dispensed in thesub unit 3 toward themain unit 2. - More specifically, as shown in
FIG. 2 , themain unit 2 includes amain storage part 20 and amedicine packing part 21. Amedicine path 22 connecting the main storage part and the medicine packing part is formed in the main unit. A medicinestandby mechanism part 50 and amedicine preparing part 80, which will be described in detail below, form a middle section of themedicine path 22. Further, as shown inFIG. 1 , themain unit 2 includes a manual distributingunit 23 independent from themain storage part 20. Medicines to be prescribed can be also fed into the manual distributingunit 23. That is, themain unit 2 includes themain storage part 20 and the manual distributingunit 23 as a medicine dispensing means capable of dispensing the medicines according to a prescription. - The
main storage part 20 has adrum 31 having a plurality of vertically elongatedplate members 30 that are circumferentially arranged as shown inFIG. 4( a). The main storage part is configured such that a plurality ofcassettes 32 for accommodating tablets are attached to an outer peripheral surface of thedrum 31 as shown inFIG. 4( b). In theplate members 30, a plurality ofcassette attaching holes 35, for attaching thecassette 32, andopenings 36 communicating with a dispensingpath 33 are formed along a length direction (upward and downward direction) to correspond to an attachment position of thecassettes 32. In themain storage part 20 employed in the present embodiment, a plurality of thecassettes 32 are juxtaposed along a lengthwise direction (upward and downward direction) of theplate member 30 as well as around the circumference of thedrum 31. - Each of the
plate members 30 is attached through a hinge to a frame that makes up a framework of thedrum 31 at its upper end portion. When performing maintenance on themain storage part 20, each of the plate members is maintained in a raised state by lifting a lower end portion of each of theplate members 30 and thedrum 31 can be opened. - Further, as shown in
FIG. 4 , an inner side (an inner peripheral surface) of thedrum 31 is provided with the dispensingpath 33. The dispensingpath 33 serves as a path for feeding the medicines dispensed from thecassette 32 to a further downstream side. More specifically, to a rear side of theplate member 30, that is, a surface facing the inside of thedrum 31 is provided with aguide member 37. Theguide member 37 has an approximately U-shaped cross-section and is an elongated member similar to theplate member 30. Theguide member 37 is fixed to the rear side of theplate member 30 and an approximate center portion of theplate member 30 in a widthwise direction thereof (in a circumferential direction of the drum 31). Thus, the dispensingpath 33, which extends straight along a lengthwise direction of the plate member 30 (i.e., along an upward and downward direction), is formed between theguide member 37 and the rear surface of theplate member 30. - As shown in
FIGS. 4( b) and 5, a main portion of thecassette 32 includes a motor base (container mounting part) 40 and a feeder container (medicine feeding container) 41. Themotor base 40 includes amotor 43. Anoutput shaft 45 is attached to the motor to upwardly project from themotor base 40. Also, theoutput shaft 45 is provided with agear 46. Further, themotor base 40 contains a reader-writer (an interface means) 44. The reader-writer 44 corresponds to a communication mechanism referred to as an RFID (Radio Frequency Identification). The reader-writer is configured to communicate with atag 49 provided in the feeder container 41 (this will be described in detail below) to read and write a data necessary for thetag 49. - The
feeder container 41 is disposed above themotor base 40 and is configured to be detachable relative to themotor base 40. As shown inFIGS. 5 and 6 , thefeeder container 41 is a hollow container formed by mounting anopening attachment 41 b and alid attachment 41 c on acontainer body portion 41 a. The feeder container is configured to be capable of accommodating medicines therein. As shown inFIG. 6 , thecontainer body portion 41 has an openingattachment mounting portion 41 d capable of mounting theopening attachment 41 b at its back side (i.e., a side facing toward thedrum 31 when thefeeder container 41 is attached to the motor bases 40 mounted on the drum 31). - The
opening attachment 41 b is configured to be mounted to the openingattachment mounting portion 41 d of thecontainer body portion 41 a. Theopening attachment 41 b has anopening 47 a for discharging the medicines accommodated in thefeeder container 41 and atag attaching portion 47 b. In thefeeder container 41 employed in the present embodiment, various kinds of the openingattachments 41 b with different sizes ofopenings 47 a are prepared. Thus, according to a size of the medicine to be accommodated in thecontainer body portion 41 a, a suitable opening attachment can be selected and mounted. Thetag attaching portion 47 b is formed at a lower side of theopening attachment 41 b in a cantilever shape. When theopening attachment 41 b is mounted to the openingattachment mounting portion 41 d, thetag attaching portion 47 b becomes parallel to a bottom surface of thecontainer body portion 41 a. - The
lid attachment 41 c is configured to close an open portion of an upper end side of thecontainer body portion 41 a. Thelid attachment 41 c has alid portion 41 f, aclip potion 41 g and ahinge portion 41 h. Thelid portion 41 f and theclip portion 41 g are bendably connected to each other through thehinge portion 41 h. Thelid attachment 41 c is mounted by fitting a lidattachment mounting portion 41 e provided at an upper end of thecontainer body portion 41 a to theclip portion 41 g. Thefeeder container 41 can open thecontainer body portion 41 a by erecting thelid portion 41 f as shown inFIGS. 5 and 6 and can close thecontainer body portion 41 a by laying down the lid portion as shown inFIG. 4( b). - As shown in
FIG. 4( b), arotor 48 is disposed in thefeeder container 41. A plurality ofgrooves 48 extending in an upward and downward direction are circumferentially formed at an outer periphery of therotor 48 at an approximately equal interval. Therotor 48 is configured to freely rotate in thefeeder container 41. As the rotor rotates, thegrooves 48 a reach a position of anopening 47 a formed at a back side of thefeeder container 41 one after another. In the present embodiment, various kinds of therotors 48 with different widths ofgrooves 48 a are prepared. Thus, according to the size of the medicine to be accommodated in thecontainer body portion 41 a, a suitable rotor may be selected and mounted. That is, in the present embodiment, a width (a length in a circumferential direction of the rotor 48) and depth (a length along a diameter of the rotor 48) of thegroove 48 a is sized such that one of the medicines accommodated in thecontainer body portion 41 a can pass through the groove one by one. - The
rotor 48 is connected to agear 48 b exposed on a bottom surface of thefeeder container 41. When thefeeder container 41 is mounted on themotor base 40, thegear 48 b is allowed to mesh with agear 46 of themotor base 40. As a result, as themotor 43 provided in themotor base 40 operates, therotor 48 rotates within thefeeder container 41 as much as a rotation quantity of theoutput shaft 45. Thus, thecassette 32 is configured to appropriately adjust a quantity of the medicines dispensed from the opening 47 a of thefeeder container 41 by adjusting the amount of rotation of theoutput shaft 45 of themotor 43. - When the
opening attachment 41 b and thelid attachment 41 c are attached as described above, thetag attaching portion 47 b comes to a position which becomes a bottom surface of thefeeder container 41. Thetag attaching portion 47 b is provided with a tag (an information recordable medium) 49. In the present embodiment, as thetag 49, an RFID tag or an RFID chip is employed as thetag 49. Various data including an identification data of thefeeder container 41 and the kinds of medicines to be accommodated in thefeeder container 41 can be transmitted to and received from thetag 49. The data of the tag can be renewed or written. - Further, as shown in
FIG. 4( a) andFIG. 4( c), an abnormalset detecting means 38 is provided at an outer side of thedrum 31. The abnormalset detecting means 38 includes acontact plate 38 a and aswitch 38 b. The abnormalset detecting means 38 is configured to detect an abnormal attachment of thecassette 32 to thedrum 31 based on whether or not theswitch 38 b is turned on. - Configuration of the abnormal
set detecting means 38 will be described in detail as follows. As shown inFIG. 4( a), thecontact plate 38 a is an elongated plate body. Thecontact plate 38 a is disposed along a height direction of thedrum 31. Thecontact plate 38 a is shaft-supported on a housing of themain unit 2 through ahinge 38 c in a cantilever shape. An end of the contact plate facing toward thedrum 31 is a free end. That is, thecontact plate 38 a is supported by thehinge 38 c so as to be capable of swinging relative to a tangential direction of thedrum 31. Further, theswitch 38 b is disposed in a position where thecontact plate 38 a contacts the switch as thecontact plate 38 a swings. If thecontact plate 38 a contacts theswitch 38 b, then a contact of the switch is pressed down and thus the switch is turned on. - As shown in
FIG. 4( c), when assuming a trajectory J, which ends of thecassettes 32 form while passing along with a rotation of thedrum 31 with thecassettes 32 attached thereto, thecontact plate 38 a is positioned slightly apart from the trajectory J in a direction of a diameter of thedrum 31 in a position where the ends of the cassettes reach. Thus, when thecassette 32 is not securely mounted on thedrum 31 and therefore projects outwardly in a direction of a diameter of thedrum 31, thecassette 32 is brought into contact with thecontact plate 38 a along with the rotation of thedrum 31 and therefore thecontact plate 38 a swings about thehinge 38 c. As a result, thecontact plate 38 a bumps against theswitch 38 b and the switch is turned on. Thus, the abnormal attachment of thecassette 32 is detected. - As shown in
FIGS. 2 and 3 , the medicinestandby mechanism part 50 is disposed below the above-describeddrum 31. As shown inFIGS. 3 and 7 , the medicinestandby mechanism part 50 includes, as a main part thereof, a funnel-shapedstandby hopper 51, amovable lid 52 and alid moving mechanism 53. Thestandby hopper 51 is attached to abox body 54 of the medicinestandby mechanism part 50. Themovable lid 52 is mounted on thelid moving mechanism 53 attached to thestandby hopper 51. - More specifically, as shown in
FIG. 7 , thestandby hopper 51 has amechanism positioning part 55 for disposing thelid moving mechanism 53 in its center portion. A plurality of dischargingopenings 56 are formed in a position surrounding themechanism positioning part 55. Further, aflange 57 is formed along an outer edge portion of thestandby hopper 51. Thestandby hopper 51 is fixed to thebox body 54 by screw-fixing theflange 57 to the box body. - The
lid moving mechanism 53 is configured to move themovable lid 52 in an upward and downward direction relative to thestandby hopper 51. Thelid moving mechanism 53 has amotor 58 as a power source, amechanism part 60 operable by a power from themotor 58, and apower transmitting shaft 61 for transmitting the power of themotor 58 to themechanism part 60. Themotor 58 is positioned such that arotating shaft 58 a is approximately vertical to a side surface of thebox body 54 and projects toward an inside portion of thebox body 54. - As shown in
FIG. 8 , themechanism part 60 includes adrive part 60 a operable by the power of themotor 58 and a drivenpart 60 b operable by the power from thedrive part 60 a. Thedrive part 60 a has abevel gear 60 c coupled to a leading end of thepower transmitting shaft 61 and abevel gear 60 d disposed so as to mesh therewith. Thebevel gear 60 d is coupled to one end of arotating shaft 60 e uprightly erected vertically to thepower transmitting shaft 61. Further, adrive gear 60 f is coupled to the other end of therotating shaft 60 e and configured to be integrally rotatable with thebevel gear 60 d. Thus, if a rotation power is transmitted from themotor 58 through thepower transmitting shaft 61, thedrive gear 60 f rotates about the rotatingshaft 60 e. - Meanwhile, the driven
part 60 b has arotating cylinder member 60 g, a drivengear 60 h, acam 60 i and aslide shaft 60 j. Therotating cylinder member 60 g is a cylindrical member. The rotating cylinder member is positioned with its axial center at an approximate center of themechanism positioning part 55 and is supported so as to rotate about the axial center. Thedrive gear 60 h has a ring shape. Thedrive gear 60 h is an outwardly-toothed gear with its outer diameter approximately equal to therotating cylinder member 60 g. Thedrive gear 60 h is fixed on an upper end of therotating cylinder member 60 g. Further, thedrive gear 60 h is meshed with thedrive gear 60 f installed in thedrive part 60 a. Thus, if thedrive gear 60 f rotates by the power of themotor 58, the power is transmitted to thedrive gear 60 f, thereby rotating therotating cylinder member 60 g about its axial center. - The
cam 60 i is a so-called end cam. An end face 60 k of the cam has a shape which is formed by cutting a cylinder at a plane P intersecting its generator. More specifically, as shown inFIG. 8( b), when assuming the plane P passes theend face 60 k and thecam 60 i is disposed with theend face 60 k facing upward, theend face 60 k has anupper end 60 s located at an uppermost side and alower end 60 t located at a lowermost side. The end face is shaped such that anintermediate portion 60 u gently connects theupper end 60 s and thelower end 60 t. - The
cam 60 i is disposed inside therotating cylinder member 60 g with theend face 60 k facing upward. Thecam 60 i is integrated with therotating cylinder member 60 g to rotate along with therotating cylinder member 60 g. Theslide shaft 60 j is a shaft body connected to themovable lid 52. The slide shaft is divided into asmaller diameter portion 60 p and alarger diameter portion 60 q by aflange portion 60 m provided at one end side in a lengthwise direction. Thesmaller diameter portion 60 p is located more closely to the end side of theslide shaft 60 j than theflange portion 60 m and has a diameter smaller than other portions. - The
larger diameter portion 60 q forms a main portion of theslide shaft 60 j. Theslide shaft 60 j is configured to freely slide in an axial direction relative to thecam 60 i (i.e., an upward and downward direction) by inserting thelarger diameter portion 60 q into thecam 60 i. Aroller 60 r is rotatably coupled to a peripheral surface of thelarger diameter portion 60 q and an intermediate portion in a lengthwise direction of thelarger diameter portion 60 q. Theroller 60 r is in contact with theend face 60 k of thecam 60 i when theslide shaft 60 j is inserted into thecam 60 i with thelarger diameter portion 60 q facing downward. Thus, as thecam 60 i rotates about its axial center, theroller 60 r rolls on theend face 60 k and theslide shaft 60 j moves in an upward and downward direction to conform with an undulation of theend face 60 k. - The
slide shaft 60 j is integrated with themovable lid 52 by inserting thesmaller diameter portion 60 p into arecess 66 formed at an approximate center of themovable lid 52 and screw-fixing theflange portion 60 m to themovable lid 52. More specifically, themovable lid 52 is a disk-shaped member having an approximate circular lidtop surface 52 a and a lidperipheral surface 52 b for surrounding an outer periphery of the lid top surface. Therecess 66 is formed at an approximate center portion of the lidtop surface 52 a inside themovable lid 52. Themovable lid 52 is integrated with theslide shaft 60 j by inserting thesmaller diameter portion 60 p of theslide shaft 60 j into therecess 66 and screw-securing between the lidtop surface 52 a and theflange portion 60 m. - The
movable lid 52 moves in an upward and downward direction by operation of the above-describedlid moving mechanism 53 to thereby open and close each of the dischargingopenings 56 formed in thestandby hopper 51. More specifically, in thelid moving mechanism 53, as therotating cylinder member 60 g rotates by operation of the motor, thecam 60 i relatively rotates about the axial center relative to theslide shaft 60 j. As a result, theroller 60 r coupled to theslide shaft 60 j moves in an upward and downward direction to conform with the undulation of theend face 60 k while rolling along theend face 60 k of thecam 60 i. Accordingly, theslide shaft 60 j and themovable lid 52 integrated thereto slide upward and downward relative to thecam 60 i. - Still more specifically, as shown in
FIG. 9( a), when theroller 60 r coupled to thelarger diameter portion 60 q of theslide shaft 60 j is in contact with a position corresponding to thelower end 60 t of thecam 60 i, theslide shaft 60 j is in a lowermost position in thecam 60 i. In this case, as shown inFIG. 10( a), themovable lid 52 is in a state where alid connecting cylinder 62 of themechanism part 60 is lowered and a lower end of the lidperipheral surface 52 b is in contact with an inner peripheral surface of thestandby hopper 51. In such a state, since each of the dischargingopenings 56 formed in thestandby hopper 51 is surrounded and blocked by the lidperipheral surface 52 b, the medicines inputted into thestandby hopper 51 can be gathered. - Meanwhile, if the
motor 58 provided in thelid moving mechanism 53 operates, therotating cylinder member 60 g and thecam 60 i integrated thereto start to rotate as indicated by an arrow inFIG. 9 . As a result, as shown inFIG. 9( b), theintermediate portion 60 u of theend face 60 k comes to a position corresponding to theroller 60 r. In this case, as described above, theslide shaft 60 j is configured to freely slide upwardly and downwardly relative to thecam 60 i. Thus, if theintermediate portion 60 u comes to the position corresponding to theroller 60 r by the rotation of thecam 60 i, theslide shaft 60 j is pushed upwardly. As a result, themovable lid 52 integrated to theslide shaft 60 j is gradually pushed upward, thereby forming a gap between the lower end of the lidperipheral surface 52 b and the inner peripheral surface of thestandby hopper 51 as shown inFIG. 10( b). - Thereafter, the
cam 60 i further rotates. As shown inFIG. 9( c) andFIG. 9( d), as theintermediate portion 60 u comes to the position corresponding to theroller 60 r, a height in theend face 60 k becomes gradually higher and thus themovable lid 52 is further pushed upwardly. As a result, the gap between the lower end of themovable lid 52 integrated to theslide shaft 60 j and the inner peripheral surface of thestandby hopper 51 becomes larger. Further, if thecam 60 i rotates until theupper end 60 s of theend face 60 k comes to the position corresponding to theroller 60 r, then the gap between the lidperipheral surface 52 b and the inner peripheral surface of thestandby hopper 51 is allowed to maximally open, thereby providing a state where the medicines can sufficiently pass through, that is, a state where each of the dischargingopenings 56 is opened. - As shown in
FIG. 2 , acollecting hopper 70 is provided below the medicinestandby mechanism part 50. The collectinghopper 70 is situated so as to connect the medicinestandby mechanism part 50 and a medicine preparing part 80 (this will be described in detail below). - Further, as described above, the
main unit 2 includes the manual distributingunit 23. As shown inFIG. 1 , the manual distributingunit 23 has a plurality ofmeasures 90 arranged in a matrix form therein. Each of the measures in some embodiments is capable of accommodating multiple medicines per pack. The medicine delivering unit is configured to be drawn out from the housing of themain unit 2. An upper side of each of themeasures 90 is opened. Themedicine delivering unit 23 is configured to be appropriately drawn out from the housing of themain unit 2 so that the medicines for one pack can be fed into each of themeasures 90. When accommodated in the housing of themain unit 2, the manual distributingunit 23 can dispense the medicines by opening a bottom side of each of themeasures 90. - In a state where the manual distributing
unit 23 is accommodated in the housing of themain unit 2, a manual distributinghopper 91 is disposed below the manual distributingunit 23. The manual distributinghopper 91 is configured to feed the medicines dispensed from each of themeasures 90 of the manual distributingunit 23 to themedicine preparing part 80. - The
medicine preparing part 80 is configured to gather and prepare the medicines for one pack fed from the above describedstandby hopper 51 and the manual distributinghopper 91 and to sequentially discharge the same to a further downstream side. Themedicine preparing part 80 is disposed below the medicinegathering mechanism portion 50 and the manual distributingunit 23. As shown inFIGS. 11 and 12 , themedicine preparing part 80 has a disk-shapedsection forming body 81, a medicine preparingpart body 82 and alid 83. Thesection forming body 81 hassections 81 a for gathering the medicines. Thesection forming body 81 employed in the present embodiment has a plurality of thesections 81 a (six sections in the present embodiment) in a circumferential direction. Each of thesections 81 a is opened at a top surface of thesection forming body 81. Further, each of thesections 81 a has ashutter 81 c, which can be opened and closed independently. Theshutter 81 c is blocked at normal times, but is opened if alever 81 d provided at a lateral side of each of thesections 81 a is pressed. - More specifically, as shown in
FIG. 12 , each of thesections 81 a is surrounded by the following: afront wall portion 86 a at one end side in a circumferential direction of thesection forming body 81; arear wall portion 86 b at the other side in the circumferential direction andperipheral wall portions 86 c, 86 d at outer and inner sides in a diametrical direction of thesection forming body 81. Thefront wall portion 86 a is inclined toward an inside of thesection 81 a from a top surface of thesection forming body 81 toward a bottom surface thereof. Further, a steppedportion 86 e is formed in a portion of thefront wall portion 86 a at a bottom surface of thesection forming body 81. Therear wall portion 86 b approximately vertically extends from the top surface of thesection forming body 81 toward its bottom surface up to a middle portion and then is inclined toward an outside of thesection 81 a from the middle portion to the bottom surface. - The
shutter 81 c has a plate shape. One end (hereinafter, this may be referred to as a proximal end) of theshutter 81 c is swingably shaft-supported by asupport shaft 86 f in a position of thereal wall portion 86 b and the top surface of thesection forming body 81. The other end (hereinafter, this may be referred to as a leading end) of theshutter 81 c faces toward thefront wall portion 86 a and the bottom surface of thesection forming body 81. That is, theshutter 81 c is inclined in a downward direction in an inner space of thesection 81 a as going from the proximal end to the leading end. Theshutter 81 c is biased by a biasing means (not shown) such as a spring coupled to the leading end pressed so that the leading end can face upwardly. Further, at normal times, the leading end of theshutter 81 a is closed to the steppedportion 86 e of thefront wall portion 86 a. Thus, thesection 81 a is blocked at the bottom surface of thesection forming body 81. Thelever 81 d is integrated with theshutter 81 a by thesupport shaft 86 f. Thelever 81 d is configured to be pivot about thesupport shaft 86 f while maintaining at a constant angle relative to theshutter 81 c. Aroller 86 g is freely rotatably coupled to thelever 81 d. - As shown in
FIGS. 11 and 12 , aflange portion 81 b projecting diametrically outwardly is provided at the bottom surface of the above-describedsection forming body 81. Theflange portion 81 b has a plurality of gear teeth at its outer periphery and thus has an outwardly-toothed gear shape. A throughhole 81 e is formed in a center portion of thesection forming body 81 so as to pass through in thickness of thesection forming body 81, that is, between the top surface and the bottom surface. - The medicine preparing
part body 82 has anaccommodating part 82 a capable of accommodating thesection forming body 81. Asupport shaft 82 b projecting upwardly is disposed in an approximate center of theaccommodating part 82 a. The above-describedsection forming body 81 is mounted in theaccommodating part 82 a in such a manner that the top surface faces upward and thesupport shaft 82 is inserted through the throughhole 81 e. Thus, thesection forming body 81 is accommodated within theaccommodating part 82 a while rotatable about thesupport shaft 82 b. - Further, a
drive mechanism 84 is provided in the medicine preparingpart body 82. Thedrive mechanism 84 includes amotor 84 a and agear 84 b rotatable by power from themotor 84 a. Thegear 84 b is meshed with the gear formed in theflange portion 81 b of thesection forming body 81 accommodated in theaccommodating part 82 a. Thus, if themotor 84 a operates, the power is transmitted through thegear 84 b to thesection forming body 81 and thus thesection forming body 81 rotates about thesupport shaft 82 b. - As shown in
FIG. 12 , anopening 82 c for dispensing the medicines is formed at a bottom surface of the medicine preparingpart body 82. Theopening 82 c is formed in a position where it can communicate with each of thesections 81 a provided in thesection forming body 81. Further, alever contactor 82 d is provided in a position adjacent to theopening 82 c. More specifically, thelever contactor 82 d has a block shape. Thelever contactor 82 d is, in some embodiments, made up of an ascending-inclined portion 82 e, ahorizontal portion 82 f and a descending-inclined portion 82 g as shown by a tow-dot chain line inFIG. 13 . An upper surface of thelever contactor 82 d is inclined in the ascending-inclined portion 82 e and the descending-inclined portion 82 g, while horizontal in thehorizontal portion 82 f. The upper surface of thelever contactor 82 d is upwardly inclined in the ascending-inclined portion 82 e as going toward thehorizontal portion 82 f. The upper surface of thelever contactor 82 d is downwardly inclined in the descending-inclined portion 82 g as being spaced apart from thehorizontal portion 82 f. Thelever contactor 82 d is positioned such that the ascending-inclined portion 82 e faces upstream in a rotation direction of thesection forming body 81 and the descending-inclined portion 82 g faces downstream in the rotation direction. - The
lever contactor 82 d is positioned in the medicine preparingpart body 82 in a position where thelever contactor 82 d contacts thelever 81 d provided at a later side of each of thesections 81 a when thesection forming body 81 rotates. Thus, as shown inFIG. 13 , if thesection forming body 81 rotates and thus each of thelevers 81 d contacts thelever contactor 82 d, then theshutter 81 c connected to thelever 81 d is opened. More specifically, when thelever 81 d comes to a position where thelever contactor 82 d is provided by the rotation of thesection forming body 81, theroller 86 g coupled to the leading end of thelever 81 d is allowed to ride on the ascending-inclined portion 82 e as shown inFIG. 13( a). If thesection forming body 81 further rotates from such a state, theroller 86 g rolls on the ascending-inclined portion 82 e and an inclination of thelever 81 d becomes closer to an approximately horizontal state as shown inFIG. 13( b). - In this case, as described above, the
lever 81 d is configured to be rotatable about thesupport shaft 86 f while maintaining at a constant angle relative to theshutter 81 c. Thus, if the inclination of thelever 81 d changes as described above, theshutter 81 c rotates about thesupport shaft 86 f by such change and the leading end of theshutter 81 c becomes gradually close to therear wall portion 86 b. Thus, the bottom surface ofsection 81 a gradually becomes open. - If the rotation of the
section forming body 81 proceeds as described above, the opening extent of theshutter 81 c becomes gradually large as shown inFIG. 13( c). Thereafter, if thesection forming body 81 further rotates and theroller 86 g coupled to the leading end of thelever 81 d is positioned as shown inFIG. 13( d), theshutter 81 c becomes in contact with therear wall portion 86 b ofsection 81 a and thus theshutter 81 c becomes fully open. - If the rotation of the
section forming body 81 further proceeds from a full open state of theshutter 81 c and theroller 86 g reaches the descending-inclined portion 82 g as shown inFIG. 13( e), theshutter 81 c is biased and the leading end of theshutter 81 c becomes gradually close to thefront wall portion 86 a ofsection 81 a. Thus, the bottom surface ofsection 81 a gradually becomes closed by theshutter 81 c. And, if theroller 86 g passes over a halfway point of the descending-inclined portion 82 g, the leading end of theshutter 81 a contacts the steppedportion 86 e formed in thefront wall portion 86 a and the bottom surface ofsection 81 a becomes blocked byshutter 81 c as shown inFIG. 13( f). - The
section forming body 81 is accommodated in the medicine preparingpart body 82 so as to operate as described above. Meanwhile, apacking hopper 85 is provided in a position corresponding to theopening 82 c of the bottom surface of the medicine preparingpart body 82. Thepacking hopper 85 is provided so as to feed the medicines dispensed from theopening 82 c toward the medicine packing part 21 (this will be described in detail below). Thus, if each of thesections 81 a comes to a position corresponding to theopening 82 c in the medicine preparingpart body 82, thelever 81 d provided insection 81 a is pressed and theshutter 81 is opened. As a result, the medicines gathered insection 81 a are dispensed toward themedicine packing part 21. - Further, as shown in
FIG. 11 , an approximatelycircular opening 82 i is formed in atop plate 82 h forming the top surface of the medicine preparingpart body 82 so as to correspond to thesection forming body 81. Further, thelid 83 is provided so as to block theopening 82 i. Thelid 83 has threeholes 83 a to 83 c. Theholes 83 a to 83 c are configured to be connected to thecollecting hopper 70, the manual distributinghopper 91 and the sub collecting hopper 87 (this will be described in detail below). Theholes 83 a to 83 c are formed in a position corresponding to each of thesections 81 a of thesection forming body 81 accommodated in theaccommodating part 82 a. Thus, themedicine preparing part 80 is configured to be capable of inputting the medicines through theholes 83 a to 83 c into each of thesections 81 a provided in the medicine preparingpart body 82. - More specifically, as shown in
FIG. 14 , the collectinghopper 70 is connected to thehole 83 a formed in thelid 83. As shown inFIG. 15 , when viewed from the top surface, thehole 83 a is formed in a position deviated by onesection 81 a, which makes up thesection forming body 81, in a counterclockwise direction (a left-hand direction) from a position of theopening 82 c formed in the medicine preparingpart body 82 for dispensing the medicines. That is, when assuming that onesection 81 a provided in thesection forming body 81 coexists with theopening 82 c, thehole 83 a is formed in a position where the medicines can be inputted intosection 81 a counterclockwise in a circumferential direction of thesection forming body 81 fromsection 81 a corresponding to theopening 82 c. - As will be described in detail below, the
sub collecting hopper 87 for feeding the medicines, which are transferred from thesub unit 3 through thetransfer device 5, to themedicine preparing part 80 is connected to thehole 83 b. Thehole 83 b is formed in a position counterclockwise deviated from theopening 82 c of the medicine preparingpart body 82 by twosections 81 a constituting thesection forming body 81. That is, when assuming thatsection 81 a is positioned so as to correspond to theopening 82 c, thehole 83 b is formed in a position where the medicines can be inputted intosection 81 a counterclockwise adjacent to thesection 81 a. Further, the manual distributinghopper 91 is connected to thehole 83 c. Thehole 83 c is formed in a position clockwise (in a right-hand direction) from theopening 82 c of the medicine preparingpart body 82 by threesections 81 a. - As shown in
FIG. 14 , themedicine packing part 21 is provided below the above-describedmedicine preparing part 80. Themedicine packing part 21 includes a packing means 21 a and a conveyingmeans 21 b. The packing means 21 a includes asheet transferring mechanism 95, apack forming mechanism 96 and aprinting part 99. Thesheet transferring mechanism 95 is configured to unwind a packingpaper sheet 98, which includes a thermally fused elongated sheet and has a sheet form wound around aroll shaft 97, and to transfer it to thepack forming mechanism 96. The packingpaper sheet 98 unwound by thesheet transferring mechanism 95 is sequentially transferred along a path extending through thepack forming mechanism 96 to theprinting part 99 as indicated by an arrow inFIG. 14 and is then fed to the conveying means 21 b. Thepack forming mechanism 96 has asheet supporting part 99, aguide member 100 and apartition forming device 101. Thepack forming mechanism 96 is configured to bend the packingpaper sheet 98 transferred from thesheet transferring mechanism 95 into two portions at its approximate halfway portion in a shorter direction (width direction) and compresses the bentpacking paper sheet 98 into a pouch shape. - The
guide member 100 is provided upstream in a flowing direction of the packingpaper sheet 98 from thepacking hopper 85 provided in the bottom surface of the medicine preparingpart body 82 halfway in the flowing direction of the packingpaper sheet 98. Theguide member 100 has functions of not only serving as a guide of the packingpaper sheet 98 but also bending the elongatedpacking paper sheet 98 into two portions at an approximate halfway portion in a width direction. Thepartition forming device 101 is disposed downstream in the flowing direction of the packingpaper sheet 98 from the above-describedpacking hopper 85. Thepartition forming device 101 can compress a portion of one end side (downstream side) in a lengthwise direction of the bifoldpacking paper sheet 98, which is previously bent by theguide member 100, into a semi-pouch shape or compress and close an opening portion of the semi-pouch shaped packingpaper sheet 98 into a pouch shape. - The
printing part 99 is configured to perform a print on the packingpaper sheet 98 transferred by thesheet transferring mechanism 95. As shown inFIG. 14 , theprinting part 99 is positioned downstream in the flowing direction of the packingpaper sheet 98 from themedicine packing part 21 and upstream in the flowing direction of the packingpaper sheet 98 from thepack forming mechanism 96. A length of the packingpaper sheet 98 existing between the positions of theprinting part 99 and thepack forming mechanism 96 is n times (three times in the present embodiment) greater than a length of a medicine pack formed by compressing the packingpaper sheet 98. - As shown in
FIG. 16 , the conveying means 21 b is configured to convey the packingpaper sheet 98 with the medicines packed therein in the packing means 21 a toward dispensingopenings front panel 2 a or aside panel 2 b of themain unit 2. As shown inFIG. 17 , the conveying means 21 b has acasing 105. A conveyingmechanism 106 is equipped in thecasing 105. The conveying means 21 b includes a receivingportion 105 a, astraight portion 105 b and abent portion 105 c. As shown inFIGS. 14 , 17 and 19, the conveying means 21 b is disposed in a manner that the receivingportion 105 a is positioned at a bottom surface in the housing of themain unit 2 and a portion from thestraight portion 105 b to thebent portion 105 c erects obliquely upwardly from the receivingopening 105. - The conveying means 21 b has a serial conveying path of the packing
paper sheet 98 from the receivingportion 105 a through thestraight portion 105 b to thebent portion 105 c. As shown inFIGS. 16 and 19 , driverollers 110 are provided in several places along the conveying path formed in the conveying means 21 b. More specifically, thedrive rollers 110 are freely rotatably provided in the following places: an entrance to the receivingportion 105 a; the vicinity of a boundary between the receivingportion 105 a and thestraight portion 105 b; and the vicinity of a boundary between thestraight portion 105 b and thebent portion 105 c; and a leading end side of thebent portion 105 c. In the conveying means 21 b,belts 111 are wound between neighboringdrive rollers 110 so as to transmit a power from a motor (not shown). In the present embodiment, fourbelts 111 are provided at a predetermined interval in a lengthwise direction of eachdrive roller 110. - The receiving
portion 105 a is configured to receive the packingpaper sheet 98 with the medicines packed by the packing means 21 a and to change a transfer direction of the packingpaper sheet 98, which is transferred obliquely downward, into an obliquely upward direction. The receivingopening 105 has a receivingopening 107 a for receiving the packingpaper sheet 98 and aguide roller 107 b provided therein. The receivingportion 105 a is disposed in a position where the receivingopening 107 a can receive the serialpacking paper sheet 98 formed by packing the medicines in the packing means 21 a. - The
casing 105 is configured to allow the packingpaper sheet 98 to pass through between theguide roller 107 b and the above-describeddrive roller 110 and thebelt 111 suspended thereto at a portion corresponding to the receivingportion 105 a. Further, the receivingportion 105 a is curved along theguide roller 107 b and connected to thestraight portion 105 b. Thus, if the packingpaper sheet 98 is introduced through the receivingopening 107 a into the receivingportion 105 a in the conveying means 21 b, then the packingpaper sheet 98 is guided by theguide roller 107 b and is brought into contact with thedrive roller 110 and thebelt 111 and then the packingpaper sheet 98 is transferred toward thestraight portion 105 b. - A plurality of pressing
rollers 112 are provided at a boundary between the receivingportion 105 a and thestraight portion 105 b, thestraight portion 105 b and thebent portion 105 c. Thepressing rollers 112 are disposed at a predetermined interval with the neighboring one in a lengthwise direction of thestraight portion 105 b. Further, when assuming a conveyance plane H of the packingpaper sheet 98 formed by thedrive roller 110 and thebelt 111, thepressing roller 112 presses the conveyance plane H with such a pressure force as the belt 11 slightly flexes. Further, thepressing roller 112 is biased toward the conveyance plane H. Thus, if the packingpaper sheet 98 is introduced through the receivingportion 105 a, the packingpaper sheet 98 is under pressure toward the conveyance plane H by thepressing roller 112 and the packingpaper sheet 98 receives a power from thedrive roller 110 and thebelt 111 to be transferred downstream. - In this case, as described above, a plurality of the
pressing rollers 112 are provided in the conveying means 21 a. Meanwhile, as shown inFIG. 18( b), asub roller 115 a is provided at a lateral side of thepressing roller 112 closer to the receivingportion 105 a (hereinafter, where necessary, this may be referred to as thepressing roller 112 a). Thesub roller 115 a constitutes a transfer abnormality detecting mechanism (detecting means) 115 for detecting a transfer abnormality of the packingpaper sheet 98. The sub roller is provided so as to be rotatable independently of thepressing roller 112 a. - As shown in
FIG. 18 , theabnormality detecting mechanism 115 has a pinch roller (detecting means) 115 b, ashaft 115 c and a rotary encoder (rotary detecting means) 115 d in addition to the above-describedsub roller 115 a. Thepinch roller 115 b is disposed such that the above-described conveyance plane H is interposed between the pinch roller and thesub roller 115 a. Thepinch roller 115 b is coupled to one end of theshaft 115 c and is rotatable integrally with theshaft 115 c. Thus, if the packingpaper sheet 98 passes along the conveyance plane H, thepinch roller 115 b and theshaft 115 c integrally rotate since they are pushed by the packingpaper sheet 98. - In this case, as described above, the
sub roller 115 a is configured to be rotatable independently of thepressing roller 112 a. Thus, although the belt 11 operates and thepressing roller 112 a rotates by the power from thebelt 111, thesub roller 115 a does not rotate. Thus, thesub roller 115 a and thepinch roller 115 b do not rotate as far as the packingpaper sheet 98 does not pass therebetween. - As shown in
FIGS. 18( b) and 18(c), therotary encoder 115 d has anencoder disc 115 e with a plurality ofslits 115 g circumferentially formed and aphoto interrupter 115 f like a conventional one. Further, theencoder disc 115 e is integrally coupled to the other end of the above-describedshaft 115 c. Thus, theencoder disc 115 e rotates along with thepinch roller 115 b. Accordingly, when the packingpaper sheet 98 passes through a position where thepressing roller 112 a is provided, a rotation is detected by therotary encoder 115 d. On the contrary, when thepinch roller 115 b does not rotate since the packingpaper sheet 98 causes a transfer abnormality of the packing paper sheet such as a paper jam, a rotation is not detected in therotary decoder 115 d. - As shown in
FIG. 17 , thebent portion 105 c is connected to thestraight portion 105 b through asupport shaft 110 a of thedrive roller 110 provided at a distal end of thestraight portion 105 b. The bent portion can bend about thesupport shaft 110 a relative to thestraight portion 105 b. As shown inFIG. 16 , when thebent portion 105 c extends straight out to follow thestraight portion 105 b, its leading end faces toward the dispensingopening 2 d formed in theside panel 2 b of themain unit 2. Meanwhile, when thebent portion 105 c is bent toward thefront panel 2 a relative to thestraight portion 105 b, its leading end faces toward the dispensingopening 2 c. - As shown in
FIG. 1 , themain unit 2 has aworktable 117 at a later side of the above-describedmanual distributing unit 23. Where necessary, theworktable 117 can be drawn out from a main body of themain unit 2 or pushed into the main body of the main unit to be accommodated therein. As shown inFIG. 20 , theworktable 117 has acontainer placing portion 117 a capable of placing thefeeder container 41 which constitutes the above-describedcassette 32. Thecontainer placing portion 117 a has arecess 117 b which is concave to correspond to a shape of the bottom surface of thefeeder container 41. Further, when the bottom surface of thefeeder container 41 is fitted into therecess 117 b, the reader-writer 117 c is positioned in a positionopposite tag 49 in the bottoms side of thefeeder container 41. The reader-writer 117 c corresponds to a communication mechanism referred to as a RFID (Radio Frequency Identification). The reader-writer can read and write necessary data by communication with thetag 49. - As shown in
FIG. 1 , anoperation panel 118 a for operating themedicine dispensing system 1, abarcode reader 118 b and ajournal printer 118 c are provided at a front side of themain unit 2. Thebarcode reader 118 b is capable of reading barcodes written on an original medicine box. Further, thejournal printer 118 c is provided in order to print prescription records of medicines done by themedicine dispensing system 1. According to themedicine dispensing system 1, the barcodes are read by thebarcode reader 118 b to thereby operate thedrum 31 so that thecassette 32 provided in order to accommodate the medicines corresponding to the barcodes can come to the front side. - As shown in
FIGS. 1 and 2 , themedicine dispensing system 1 according to the present embodiment is configured to add thesub unit 3 to themain unit 2 configured as above. Thesub unit 3 includes asub storage part 120 capable of accommodating and appropriately dispensing medicines, which has the same configuration as themain storage part 20 of the above-describedmain unit 2. That is, in themedicine dispensing system 1 according to the present embodiment, thesub storage part 120 constitutes the medicine dispensing means together with themain storage part 20 and the manual distributingunit 23 at themain unit 2. Further, a submedicine standby part 130, which has the same configuration of the medicinestandby mechanism part 50 provided in themain unit 2, is provided below thesub storage part 120. Also, asub hopper 135 is disposed below the submedicine standby part 130. Thus, medicines dispensed from the submedicine standby part 130 can be fed through thesub hopper 135 to thetransfer device 5, which will be described in detail below. - The
sub unit 3 is configured to select thecassette 32 accommodating the medicines according to the prescription from a plurality of thecassettes 32 provided in thesub storage part 120, to operate thecassette 32 and to dispense the medicines as much as a required quantity. Further, thesub unit 3 can gather the medicines dispensed from thesub storage part 120 one pack at a time in the submain storage part 130 and dispense the same one after another through thesub hopper 135 to thetransfer device 5. - The
transfer device 5 is configured to transfer the medicines from thesub unit 3 constituting the sub unit toward themain unit 2 constituting the main unit. As shown inFIG. 21 , thetransfer device 5 has apipe line 140 and a suction means (transfer means) 141. Each component member based on thepipe line 140 are set on in asupport 144. As shown inFIG. 2 , thetransfer device 5 is positioned in a manner that thesupport 144 is inserted through acommunication opening 4 b formed in awall surface 4 a existing at a boundary between themain unit 2 and thesub unit 3 to lie across themain unit 2 and thesub unit 3. - Configuration of the
transfer device 5 will be described in detail below. Amedicine receiving part 142 is provided at one end of thepipe line 140, while amedicine dispensing part 143 is provided at the other side. The suction means 141 is pipe-connected to a suction means connectingportion 148 provided at the other side of thepipe line 140, i.e., in a position of themedicine dispensing part 143. Further, the suction means connectingportion 148 serves as a joint for connecting thepipe line 140 and a pipe connected to the suction means 141. Thus, thetransfer device 5 is configured to suck the medicines existing in themedicine receiving part 142 in thepipe line 140 to themedicine dispensing part 143 when the suction means 141 operates. - The
medicine receiving part 142 is provided with ameasure 145 for receiving the medicines and aninlet shutter mechanism 146. As shown inFIG. 21 , themeasure 145 has an opening at a top surface. The medicines transferred through thesub hopper 135 provided at thesub unit 3 can be inputted through the opening to an inside portion of themeasure 145. Meanwhile, themeasure 145 has amedicine dispensing opening 145 a at aside portion 145 b. Further, in a position opposite the opening 145 a, the one end of thepipe line 140 is disposed through ashutter plate 146 a constituting theinlet shutter mechanism 146. - In addition to the
shutter plate 146 a, theinlet shutter mechanism 146 has amotor 146 b for operating theshutter plate 146 a. A pinion (not shown) is coupled to an output shaft of themotor 146 b. Meanwhile, theshutter plate 146 a has arectangular opening 146 f opened in a rectangular shape. One edge of therectangular opening 146 f is serrated, thereby forming arack 146 c extending in a lengthwise direction of theshutter plate 146 a. Further, theshutter plate 146 a has anopening 146 e in a position adjacent to therectangular opening 146 f in a lengthwise direction. Theopening 146 e has an approximately circular opening shape and is formed in an appropriate center portion of theshutter plate 146 a. An opening diameter of theopening 146 e is approximately equal to an opening diameter of thepipe line 140. - The
shutter plate 146 a is disposed to follow theside portion 145 b of themeasure 145. Themotor 146 b is provided in a position adjacent to theshutter plate 146 a. The pinion coupled to the output shaft of themotor 146 b is positioned within therectangular opening 146 f of theshutter plate 146 a and is meshed with therack 146 c. Meanwhile, braces 150 a are provided in positions adjacent to both lateral sides of thepipe line 140. Tworollers 150 b are vertically and rotatably provided in therespective braces 150 a. Theshutter plate 146 a is supported as fitted between therollers 150 b vertically juxtaposed in eachbrace 150 a. Thus, if the pinion (not shown) rotates by an operation of themotor 146 b, theshutter plate 146 a slides along theside portion 145 b of themeasure 145. - If the
shutter plate 146 a slides by the operation of themotor 146 b up to a position where the opening 145 a of themeasure 145 coexist with theopening 146 e of theshutter plate 146 e, then themeasure 145 is allowed to communicate with thepipe line 140. On the contrary, as shown inFIG. 21( b), if theopenings shutter plate 146 a opposed to therectangular opening 146 f through theopening 146 e comes to a position corresponding to theopening 145 a of themeasure 145, then the opening 145 a becomes blocked by theshutter plate 146 a. - The
medicine dispensing part 143 is a part for dispensing the medicines conveyed from themedicine receiving part 142 through thepipe line 140. The medicine dispensing part 14 has anoutlet shutter mechanism 147. As shown inFIG. 23 , the end of thepipe line 140 is blocked at themedicine dispensing part 143. A large number offine openings 140 b are formed in a periphery of thepipe line 140 at an upper side in an assemble state of the pipe line. Further, a dispensing opening 140 a is formed in the periphery of thepipe line 140 at a side opposed to a portion where thefine opening 140 b is formed. - As shown in
FIG. 23 , theoutlet shutter mechanism 147 has ajacket 147 a, ashutter tube 147 b, amotor 147 c and agear 147 d. Thejacket 147 a has a tube-shapedjacket body 147 e and abranch portion 147 f. One end of thejacket body 147 e is blocked and is mounted on the end of thepipe line 140. Thejacket body 147 e and thebranch portion 147 f communicate with each other. In thejacket body 147 e, the above-describedfine openings 140 b face toward thebranch portion 147 f. The end of thepipe line 140 is inserted to the jacket body. Further, as shown inFIG. 21 , the suction means connectingportion 148 is connected to thebranch portion 147 f. - The
shutter tube 147 b has atube portion 147 g and agear 147 h provided in an outer periphery of the tube portion. The tube portion and thegear 147 h are integrally formed. Thetube portion 147 g is positioned between the outer periphery of thepipe line 140 and an inner periphery of thejacket body 147 e and rotatable therebetween in a circumferential direction of thepipe line 140. Further, thetube portion 147 g is provided with anopening 147 i having the same size and shape as the dispensing opening 140 a formed in the end of thepipe line 140. Thegear 147 h is provided at one end of thetube portion 147 g and exposed outwardly of thejacket body 147 e. - As shown in
FIG. 23 , themotor 147 c is disposed along thepipe line 140. Agear 147 d provided in a leading end of a rotating shaft of themotor 147 c is meshed with thegear 147 h integrally provided in theshutter tube 147 b. Thus, if themotor 147 c operates, theshutter tube 147 b circumferentially rotates relative to thepipe line 140. - If the
shutter tube 147 b rotates and theopening 147 i formed in theshutter tube 147 b comes to thefine opening 140 b of thepipe line 140 as shown inFIG. 23( a), the dispensing opening 140 a becomes blocked by the peripheral surface of theshutter tube 147 b. Thus, if the suction means 141 operates in such a state, then air in thepipe line 140 is sucked through thefine openings 140 b and thus airflow flowing from themedicine receiving part 142 to themedicine dispensing part 143 is produced. Meanwhile, if theshutter tube 147 b rotates and theopening 147 i formed in thetube portion 147 g approximately coincide with the dispensing opening 140 a of thejacket body 147 e to thereby communicate with each other as shown inFIG. 23( b). The medicines having come to the end of thepipe line 140 are allowed to be downwardly disposed. Further, thefine openings 140 b become blocked. - Next, operations of the
medicine dispensing system 1 according to the present embodiment will be described in detail below. Themedicine dispensing system 1 can pack the medicines according to the prescription into the packingpaper sheet 98 one pack at a time and dispense the same by the cooperation ofmain unit 2 and thesub unit 3. More specifically, themedicine dispensing system 1 is in some embodiments configured to dispense the medicines in themain storage part 20 or the manual distributingunit 23 provided in themain unit 2 or the medicines in thesub storage part 120 provided in thesub unit 3 according to the prescription one pack at a time to themedicine preparing part 80 in themain unit 2 and then pack the medicines at themedicine packing part 21 and dispense the same. - Still more specifically, in case where medicines are prescribed by the
medicine dispensing system 1, when the medicines to be dispensed are in themain storage part 20 of themain unit 2, themotor 43 of thecassette 32 accommodating such medicines operates. As a result, the medicines accommodated in thefeeder container 41 are dispensed one pack at a time. The medicines dispensed from thefeeder container 41 drop downward through the dispensingpath 33 provided in the inside of thedrum 31 and are gathered in thestandby hopper 51 of the medicinestandby mechanism part 50. As such, when the medicines in themain unit 2 corresponding to a prescription for one pack are gathered in thestandby hopper 51, thelid moving mechanism 53 operates and themovable lid 52 is lifted upward. Thus, the lower end of the lidperipheral surface 52 b of themovable lid 52 is spaced apart from the inner peripheral surface of thestandby hopper 51 and thus the medicines blocked by the lidperipheral surface 52 b fall down toward the dischargingopening 56. The medicines reaching the dischargingopening 56 are dispensed through thecollecting hopper 70 provided below thestandby hopper 51 to themedicine preparing part 80. - Meanwhile, when the medicines to be dispensed are in the manual distributing
unit 23 of themain unit 2, the medicines are dispensed one pack at a time from the manual distributingunit 23 as well. The medicines dispensed from the manual distributingunit 23 are fed through the manual distributinghopper 91 to themedicine preparing part 80. - Further, when the medicines to be dispensed are in the
sub storage part 120 of thesub unit 3, the medicines are dispensed from thesub storage part 120 to the submedicine standby part 130, similar to a case where medicines are in themain storage part 20 of themain unit 2. That is, when medicines in thecassette 32 provided in thesub storage part 120 are prescribed, the medicines accommodated in thefeeder container 41 are dispensed one pack at a time as described above and then gathered in thestandby hopper 51 of the sub medicine standby part (medicine standby mechanism part) 130. When the medicines to be prescribed from each of thecassettes 32 provided in thesub storage part 120 are gathered in themedicine standby part 130, thelid moving mechanism 53 of the submedicine standby part 130 operates and thus themovable lid 52 is lifted upward. Thus, the medicines gathered in the submedicine standby part 130 are dispensed through the dischargingopening 56 and thesub hopper 135 to themeasure 145 of thetransfer device 5. - When the medicines are dispensed to the
measure 145, themotor 146 b of theinlet shutter mechanism 146 provided in the vicinity of themedicine receiving part 142 operates to slide theshutter plate 146 a and the suction means 141 operates. Further, in themedicine dispensing part 143, the dispensing opening 140 a of thepipe line 140 is blocked by the peripheral surface of theshutter tube 147 b, while theopening 147 i formed in the peripheral surface of theshutter tube 147 b communicates with thefine openings 140 b formed in the peripheral surface of thepipe line 140. Then, if theopening 146 e of theshutter plate 146 a communicates with theopenings 145 a formed in theside portion 145 b of themeasure 145, the medicines dispensed in themeasure 145 are drawn into thepipe line 140. Thereafter, themotor 146 b operates in a reverse direction to the above-described embodiment and theopening 145 a of themeasure 145 is blocked by theshutter plate 146 a. - The medicines drawn into the
pipe line 140 as described above further move toward themedicine dispensing part 143 in thepipe line 140. If the medicines reach themedicine dispensing part 143, the suction means 141 is stopped. Then, theoutlet shutter mechanism 147 provided in the vicinity of themedicine dispensing part 143 operates to open the dispensing opening 140 a. That is, themotor 147 a operates to rotate theshutter tube 147 b in a circumferential direction and thus theopening 147 i formed in theshutter tube 147 b is allowed to communicate with the dispensing opening 140 a of thepipe line 140. Thus, the medicines conveyed from thesub unit 3 are dispensed through the dispensing opening 140 a to thesub collecting hopper 87. The medicines dispensed to thesub collecting hopper 87 are received insection 81 a of thesection forming body 81 provided in themedicine preparing part 80. - In the
medicine dispensing system 1 according to the present embodiment, the medicines for one pack are dispensed from themain storage part 20, the manual distributingunit 23 and thesub storage part 120 are gathered insection 81 a of thesection forming body 81 provided in themedicine preparing part 80. After gathered therein, the medicines are dispensed to themedicine packing part 21. Further, as described above, in themedicine dispensing system 1, the collectinghopper 70, the manual distributinghopper 91 and thesub collecting hopper 87, which are provided in order to feed the medicines from each of the parts to themedicine preparing part 80, are provided in positions circumferentially deviated in thelid 83 of themedicine preparing part 80. Thus, in themedicine dispensing system 1, the timing for dispensing the medicines from themain storage part 20, the manual distributingunit 23 and thesub storage part 23 toward themedicine preparing part 80 are different. - More specifically, as for six
sections 81 a provided in thesection forming body 81, when onesection 81 a corresponding to thehole 83 a as indicated by “1” inFIG. 15( a) is set as afirst section 81 a (corresponding to section A), the other fivesections 81 a are arranged counterclockwise relative to thefirst section 81 a as indicated by “2” to “6” inFIG. 15( a) when thesection forming body 81 is viewed from the top down. When assuming that thesections 81 a indicated by “2” to “6” inFIG. 15( a) are set as second tosixth sections 81 a, the medicines to be dispensed are fed through thecollecting hopper 70 from themain storage part 20 in a state shown inFIG. 15( a) (hereinafter, this may be referred to as a first rotation state). Thus, when the medicines are drawn into thefirst section 81 a, thedrive mechanism 84 operates and thesection forming body 81 rotates counterclockwise by 60 degrees. As a result, thefirst section 81 a comes to a position corresponding to thehole 83 b as shown inFIG. 15( b) and thesixth section 81 a comes to a position corresponding to thehole 83 a (hereinafter, this may be referred to as a second rotation state). - In the second rotation state, in case there are medicines to be dispensed from the
sub storage part 120 to thefirst section 81 a, thetransfer device 5 operates to supply the medicines. Further, in the second rotation state, in case there are medicines to be dispensed from themain storage part 20 to thesixth section 81 a, such medicines are dispensed through thecollecting hopper 70. If the medicines are dispensed from themain storage part 20 or thesub storage part 120 as described above thensection forming body 81 sequentially rotates counterclockwise. The second rotation state changes into a state shown inFIG. 15( c) (hereinafter, this may be referred to as a third rotation state). - In the third rotation state, the
first section 81 a comes to a position corresponding to thehole 83 c, to which the manual distributinghopper 91 is connected. In such a state, when there are medicines to be packed together with the medicines previously dispensed to thefirst section 81 a in the manual distributingunit 23, those medicines are dispensed from the manual distributingunit 23 through the manual distributinghopper 91 to thefirst section 81 a. Further, in the third rotation state, when there are medicines to be dispensed from themain storage part 20 to thefifth section 81 a or medicines to be dispensed from thesub storage part 120 to thesixth section 81 a, those medicines are dispensed through thecollecting hopper 70 or the manual distributinghopper 91. - When dispensing the medicines to each of the
sections 81 a is completed in the third rotation state as described above, the third rotation state changes into a state shown inFIG. 15( d) (hereinafter, this may be referred to as a fourth rotation state) and a state shown inFIG. 15( e) (hereinafter, this may be referred to as a fifth rotation state). During such change, similar to the first to third states, the medicines dispensed from themain storage part 20, thesub storage part 120 and the manual distributingunit 23 are inputted into each of thesections 81 a. - Then, when dispensing the medicines is completed in the fifth rotation state, the
drive mechanism 84 operates to further rotate thesection forming body 81 by 60 degrees in a clockwise direction. Thus, as shown inFIG. 15( f), thefirst section 81 a comes to a position corresponding to thehole 82 c formed in the bottom surface of the medicine preparingpart body 82. At this time, thelever 81 d provided in a position corresponding to thefirst section 81 a is brought into contact with thelever contactor 82 d provided in a position adjacent to theopening 82 c, thereby opening theshutter 81 c. Thus, while thesection forming body 81 moves in a counterclockwise direction, all the medicines gathered in thefirst section 81 a direction are dispensed through thepacking hopper 85 to themedicine packing part 21. - The medicines dispensed from the
medicine preparing part 80 to themedicine packing part 21 are accommodated in a medicine pack, which is previously formed into a semi-pouch shape by the packingpaper sheet 98. Then, the medicine pack is sealed by thepack forming mechanism 96 and the packingpaper sheet 98 is transferred by thesheet transferring mechanism 95 toward a further downstream side (toward an obliquely downward side). - In the
medicine dispensing system 1 according to the present embodiment, predetermined information on the medicine is printed by theprinting part 99 at a time (time Z) before the medicines dispensed from themedicine preparing part 80 is packed in themedicine packing part 21. More specifically, as described above, in themedicine packing part 21 employed in the present embodiment, a distance between thepack forming mechanism 96 and theprinting part 99 is set as a length corresponding to three packs of a medicine pack. Thus, at a time (time Z) as early as a time period (time period Y) required to rotate thesection forming body 81 as much as a quantity corresponding to threesections 81 a from a time (time X) when the medicines are dispensed from thefirst section 81 a, that is, in the above-described third rotation state, the information on the medicines in the third rotation state is printed by theprinting part 99. In other words, at a time (time Z) as early as the time period required for dispensing the medicines from threesections 81 a positioned upstream from thefirst section 81 a in a rotation direction of thesection forming body 81 from the timing when the medicines are dispensed from thefirst section 81 a, the information on the medicines accommodated in thefirst section 81 a is printed by theprinting part 99. - While the
section forming body 81 sequentially rotates as described above, the medicines accommodated in the first tosixth sections 81 a are dispensed one after another to themedicine packing part 21 and then packed therein and the medicines are dispensed from themain storage part 20, the manual distributingunit 23 and thesub storage part 120 to the first tosixth sections 81 a. The packingpaper sheet 98, which is formed by packing the medicines as described above, is serially transferred to the conveying means 21 b existing in the obliquely downward side. The packingpaper sheet 98 transferred to the conveying means 21 b enters an inside portion of thecasing 105 from the receivingopening 107 a formed in the receivingpart 105 a. Then, a proceeding direction of the packingpaper sheet 98, which proceeds obliquely downward in the housing of themain unit 2, changes toward an oblique upward side due to a bend in a portion of thecasing 105 corresponding to the receivingportion 105 a or guide by theguide roller 107 b. That is, the proceeding direction of the packingpaper sheet 98 changes in the receivingportion 105 a. - The packing
paper sheet 98 entering thecasing 105 is guided by theguide roller 107 b and contacts thedrive rollers 110 and thebelts 111 wound thereto. Meanwhile, thedrive rollers 110 and thebelts 111 operate by the power from a motor (not shown) provided in thecasing 105. Further, a plurality of thepressing rollers 112 are provided in a position opposed to thedrive roller 110 and thebelt 111. Thepressing rollers 112 are biased toward thebelt 111 and press thebelt 111. Thus, if the packingpaper sheet 98 is transferred from the receivingportion 105 a toward thestraight portion 105 b to thereby enter between thebelt 111 and thepressing roller 112, the packingpaper sheet 98 becomes pressed toward thedrive roller 110 and thebelt 111 by thepressing roller 112. Accordingly, if the power is transmitted from thebelt 111 to the packingpaper sheet 98, the packingpaper sheet 98 is conveyed along thestraight portion 105 toward thebent portion 105 c located obliquely upward. - The packing
paper sheet 98, which reaches thebent portion 105 c as described above, is further conveyed along thebent portion 105 c. In this case, as described above, in the conveying means 21 b employed in the present embodiment, thebent portion 105 c may be continue in a straight direction toward thestraight portion 105 with its leading end facing toward theside panel 2 b or may be bent toward thefront panel 2 a of themain unit 2 relative to thestraight portion 105 b. Thus, when thebent portion 105 c is continues in a straight direction towards thestraight portion 105 b, the packingpaper sheet 98 conveyed along thestraight portion 105 b moves straight toward theside panel 2 b and then is removed from the dispensingopening 2 d to the outside of themain unit 2. Meanwhile, when thebent portion 105 c is bent toward thefront panel 2 a, a conveying direction of the packingpaper sheet 98 conveyed along thestraight portion 105 b is directed to thefront panel 2 a and therefore the packingpaper sheet 98 is dispensed from the dispensingopening 2 c. - In the
medicine dispensing system 1 according to the present embodiment, abnormality in themedicine packing part 21 such as a paper jam of the packingpaper sheet 98 can be detected by means of theabnormality detecting means 115. More specifically, the packingpaper sheet 98 is conveyed by the conveying means 21 b in themedicine packing part 21. However, if the abnormality in transferring the packing paper sheet occurs at the conveying means 21 or at the packing means 21 a disposed more upstream than the conveying means 21 b, then the flow of the packingpaper sheet 98 is delayed in the conveying means 21 b. - Meanwhile, in the conveying means 21 b, the
sub roller 115 a is disposed near thepressing roller 112 a, which is disposed upstream in the conveying direction of the packingpaper sheet 98, that is, disposed adjacent to the receivingportion 105 a, among the plurality of pressingrollers 112. Thesub roller 115 a is rotatable independently of the pressing roller. Further, thepinch roller 115 a is disposed in a position opposed to thesub roller 115 a. Thus, when the packingpaper sheet 98 flows in themedicine packing part 21 without delays, the packingpaper sheet 98 passes between thesub roller 115 a and thepinch roller 115 a and thepinch roller 115 b is rotated by the packingpaper sheet 98. On the contrary, when the flow of the packingpaper sheet 98 in themedicine packing part 21 is stopped by any chance, the packingpaper sheet 98 does not pass between thesub roller 115 a and thepinch roller 115 b and thus thepinch roller 115 does not rotate. Thus, by detecting by means of therotary encoder 115 d connected to thepinch roller 115 b byshaft 115 c whether or not thepinch roller 115 b normally rotates, the abnormality in transferring the packingpaper sheet 98 can be detected. When the abnormality in transferring the packingpaper sheet 98 such as a paper jam is detected by theabnormality detecting mechanism 115, themedicine dispensing system 1 stops the above-described serial operations. - Further, the abnormal
set detecting means 38 is provided in themain unit 2 and thesub unit 3 employed in the present embodiment. The abnormal set detecting means is configured to detecting a case where thecassette 32 is not securely mounted on thedrum 31. More specifically, when thecassette 32 is pushed out from the trajectory J illustrated inFIG. 4( c) due to an abnormal mount, thecassette 32 bumps against thecontact plate 38 a, which constitutes the abnormal set detecting means, along with the rotation of thedrum 31 to thereby swing thecontact plate 38 a to turn on theswitch 38 b. Thus, when theswitch 38 b is turned on, themedicine dispensing system 1 judges the abnormal mount of the cassette to thereby stop the above-described serial operations. - As described above, the
medicine dispensing system 1 has themain unit 2 and thesub unit 3 and is configured to transfer the medicines dispensed from thesub storage part 120 provided in thesub unit 3 to themain unit 2 through thetransfer device 5. Further, not only are the medicines dispensed in themain unit 2 but also the medicines dispensed in thesub unit 3 can be packed in themedicine packing part 21 provided in themain unit 2 together and then be dispensed. Thus various kinds of the medicines can be dealt with by providing thesub units 3. - In this case, as described above, in the
medicine dispensing system 1, a large number of thecassettes 32 are provided installed not only in themain unit 2 but also in thesub unit 3. Thus, in some embodiments, themedicine dispensing system 1 is configured to accurately manage characteristic information on the feeder container 41 (hereinafter, this may be referred to as a characteristic container information), which constitutes eachcassette 32. More specifically, it is preferred that themedicine dispensing system 1 is configured to record the characteristic container information such as data on the kind or quantity of the medicines accommodated in thefeeder container 41 of eachcassette 32, data on a supplement history related to a person performing a medicine supplement in eachfeeder container 41 and date and time of the medicine supplement, data on a usage history of each cassette, and the like into thetag 49. Further, themedicine dispensing system 1 may be configured to manage the medicines accommodated in eachfeeder container 41 or notify a user of a maintenance time of eachcassette 32 based on the characteristic container information of each cassette recorded in thetag 49. Thus, in order to meet such a demand, as shown inFIG. 20 , there is provided adata management system 180 configured to transmit and receive the data including the characteristic container information to and from thetag 49, to renew and write the data and to read the data from thetag 49, by a control means 170 provided for controlling the operations of themedicine dispensing system 1 and either the reader-writer 49 contained in themotor base 40 which constitutes eachcassette 32 or the reader-writer 117 c provided in theworktable 117. Thedata management system 180 manages the characteristic container information of eachcassette 32. Hereinafter, a data management method performed by means of thedata management system 180 in themedicine dispensing system 1 and the operations of themedicine dispensing system 1 will be described in detail below according to an order of medicine filling. - In the
medicine dispensing system 1, the medicine filling for themain storage part 20 and thesub storage part 120 is performed by removing thefeeder container 41 of eachcassette 32 assigned to every medicine. In this case, when thecassette 32 accommodating medicines for medicine filling is in a place where a user can easily remove thefeeder container 41, thefeeder container 41 can be removed as it is. However, it may be in a place where a user cannot easily remove it. In such a case, theoperation panel 118 a is manipulated and an interface for calling the cassette shown inFIG. 22( a) is displayed. A number individually assigned to eachcassette 32 is inputted through the interface and thus thefeeder container 41 of the desiredcassette 32 can come to a place where a user can easily remove thefeeder container 41. Further, when the kind of medicines for medicine filling can be specified, theoperation panel 118 a is first manipulated and then an interface for calling a medicine name shown inFIG. 22( b) is displayed. In such a state, the medicine name can be inputted by manually inputting the kind of the medicines for medicine filling through theoperation panel 118 a or be inputted automatically by reading a particular barcode for each medicine assigned to the original medicine box by means of thebarcode reader 118 b. By dosing so, it is possible to move thefeeder container 41 of thecassette 32 accommodating the medicines for medicine filling to a place where the user can easily remove thefeeder container 41. - The
feeder container 41 of thecassette 32 removed from themain storage part 20 or thesub storage part 120 as described above is positioned so as to be fitted in therecess 117 b formed in theworktable 117. Then, thetag 49 provided at the bottom surface of thefeeder container 41 comes to a position corresponding to the reader-writer 117 c provided at theworktable 117. Thus, data communication becomes possible through the reader-writer 117 c between thetag 49 and the control means 170 of themedicine dispensing system 1. Further, in such a stage, an interface for indicating the characteristic container information shown inFIG. 22( c) andFIG. 22( d) is displayed in theoperation panel 118 a provided at the front side of themain unit 2 and thus the characteristic container information is displayed. Thus, an operation mode of themedicine dispensing system 1 is changed from a general operation mode for packing and dispensing medicines according to a prescription to a medicine filling mode for filling thefeeder container 41 with medicines. - If the operation mode of the
medicine dispensing system 1 is changed into the medicine filling mode, the characteristic container information is read from thetag 49 of thefeeder container 41 disposed on theworktable 117 through the reader-writer 117 c. More specifically, except when there is no data in thetag 49 such as right after starting to use thefeeder container 41, the characteristic container information such as data on the kind or quantity of the medicines accommodated in thefeeder container 41 of eachcassette 32, data on a supplement history related to a person carrying out a medicine supplement in eachfeeder container 41 and date and time of the medicine supplement, data on a usage history of each cassette, and the like is recorded in thetag 49. Thus, when thefeeder container 41 is fitted to therecess 117 b of theworktable 117, the characteristic container information including the above-described data is read from thetag 49 through the reader-writer 117 c to the control means 170 of themedicine dispensing system 1. The data read from thetag 49 as described above is recorded by the control means 170 into a record means 175 including a conventional memory or a hard disk. - When a screen display is made as shown in
FIG. 22( c) andFIG. 22( d), it is possible to input the information such as the kind or quantity of the medicines for medicine filling in thefeeder container 41 and an operator's name carrying out the filling operation as the characteristic container information. Regarding inputting the kind of the medicines, the operator carrying out the filling operation can manually input information. Further, it is possible to specify the kind of the medicines in the control means 170 by reading the barcode, which is written on the original medicine box of the medicine for medicine filling, by means of the barcode reader (identification mark reading means) 118 b. Further, it is possible to input the kind of the medicine by means of such an operation. - Further, for the operator's name carrying out the filling operation of the medicines, the operator can manually input like kinds of medicines. Further, in the present embodiment, for example, information for specifying the operator (operator specifying information), which is recorded in an employee card, an ID card, a ring or a wrist band assigned to each operator, is read by the
barcode reader 118 b or the reader-writer 117 c. The operator's name may be automatically inputted to the control means 170 using this information. - Further, when the
tag 49 provided in the bottom surface of thefeeder container 41 is allowed to data-communicate with the control means 170 of themedicine dispensing system 1 through the reader-writer 117 c, the characteristic container information on the usage history such as a total rotation quantity and a total rotation time of therotor 48 provided in thefeeder container 41 is read in the control means 170 in addition to the data related to the medicines accommodated in thefeeder container 41 such as the kind or quantity of the medicines or the data related to the supplement history of the medicines to thefeeder container 41. Based on the data related to the usage history of thecassette 32, the control means 170 judges whether thecassette 32 reaches a durable term or a maintenance time. Further, if it is ascertained that thecassette 32 reaches the durable term or that it is time for maintenance to be performed, a warning to that effect is displayed in theoperation panel 118 a. - In the
medicine dispensing system 1 according to the present embodiment, if thefeeder container 41 of eachcassette 32 is filled with medicines as described above and is set in themotor base 40, then the data-communication is performed between thetag 49 of thefeeder container 41 and the control means 170 through the reader-writer 44 provided in themotor base 40. Thus, a filling recording information that afeeder container 41 of which cassettes 32 among thecassettes 32 is filled with what medicines and how much the feeder container is filled is grasped by the control means 170 for eachcassette 32. Thereafter, a dispensing history of the medicine in each cassette is written into thetag 49 through the reader-writer 44 on occasions. Thus, the control means 170 can grasp a remaining quantity of the medicines in thefeeder container 41 of eachcassette 32 based on the filling quantity in thefeeder container 41 of eachcassette 32 with the medicines and the dispensing history of the medicines written in thetag 49. Further, themedicine dispensing system 1 can grasp and manage statistical information such as when and how much any medicines are used based on the filling history or the dispensing history of the medicines grasped by the control means 170 as described above. - The above-described
medicine dispensing system 1 has a function of continuously packing many predetermined medicines through an operation mode referred to as a group packing mode (i.e., a preliminary prescribing function), in addition to the function of packing medicines through the general operation mode where the medicines are prescribed based on the prescription inputted by a doctor or pharmacist. Thus, for example, it is possible to preliminarily pack many general-purpose medicines such as refrigerant medicines, analgesic medicines and stomach medicines per dosage. When themedicine dispensing system 1 operates in the group packing mode, the control means 170 confirms whether there is anycassette 32 accommodating the medicines to be packed among a large number of thecassettes 32 provided in themain storage part 20 or thesub storage part 120. In this case, when thefeeder container 41 of eachcassette 32 is replaced before the medicine dispensing system operates in the group packing mode, the characteristic container information recorded in thetag 49 provided in such afeeder container 41 is read through the reader-writer 44 contained in themotor base 40. Then, the control means 17 specifies thecassette 32 including thefeeder container 41, which accommodates the medicines to be packed through the group packing mode, and then the medicines are dispensed from thecassette 32 by a predetermined quantity. The medicines dispensed from thecassette 32 are packed in themedicine packing part 21. - As described above, the
medicine dispensing system 1 has adata management system 180 and is configured such that thetag 49 provided in everyfeeder container 41 of eachcassette 32 and the control means 170 can data-communicate with each other through the reader-writer 118 c and the characteristic container information characteristic in eachfeeder container 41 can be read from thetag 49 or written into thetag 49. Thus, it is possible to simply and accurately manage, renew and grasp the characteristic container information for eachfeeder container 41. - As described above, the reader-
writer 44 is contained in themotor base 40 of each cassette and it is possible to data-communicate with thetag 49 provided in thefeeder container 41 through the reader-writer without contact with the tag. Thus, in themedicine dispensing system 1, even if thefeeder container 41 is mounted on themotor base 40, the data such as the dispensing history of the medicines recorded in thetag 49 can be appropriately renewed. This can be effectively used for a stock management of medicines. Further, it is illustrated in the above-described embodiment that the reader-writer 44 is provided in eachcassette 32. The present invention should not be limited to such a configuration. The reader-writer 44 may be provided in some or all of thecassettes 32. - In the above-described embodiment, the reader-
writer cassette 32 or theworktable 117, which constitutes themedicine dispensing system 1, and it is possible to access to thetag 49 provided in thefeeder container 41 and read and write the data from and into the tag through the reader-writer medicine dispensing system 1 accesses thetag 49 and reads and writes the data from and into the tag, and the data written in thetag 49 is read through the reader-writer - More specifically, by way of an example of the above-described device provided separately from the
medicine dispensing system 1, a counter device 195 shown inFIG. 24 can be employed. Thecounter device 185 has abody portion 186 and acontainer attaching portion 187. A control device (not shown) for controlling operations of thecounter device 185 is provided in thebody portion 186. Further, a container placing portion and anoperation panel 189 are provided at a top surface of thebody portion 186. The container placing portion is a portion for placing the container for accommodating medicines thereon. Further, theoperation panel 189 is provided with buttons for inputting operation conditions or operation commands, such as a ten key 189 a for inputting a quantity; astart button 189 b for starting the operation; atemporary stop button 189 c for temporarily stopping the operation; and astop button 189 d for stopping the operation. In addition to the above-described-mentioned buttons, theoperation panel 189 is further provided with buttons such as awrite button 189 e and amaintenance button 189 f and adisplay 189 g. - The
container attaching portion 187 is provided with an equivalent of the above-describedmotor base 40 of thecassette 32 and adispensing opening 196. Afeeder container 41, which is removed from themain storage part 20 or thesub storage part 120 of themedicine dispensing system 1, or which is separately prepared, can be mounted on themotor base 40. Medicines can be dispensed from thefeeder container 41 by operating amotor 43 contained in themotor base 40. Further, a medicine path (not shown), through which the medicines dispensed from thefeeder container 41 attached to themotor base 40 pass, is provided in thecontainer attaching portion 187. Also, the medicine path communicates with the dispensingopening 196. Thus, the medicines, which are dispensed from thefeeder container 41 to thereby pass through the medicine path, are discharged through the dispensingopening 196 toward thecontainer placing portion 188. In thecontainer attaching portion 187, more specifically, in a suitable place such as the above-described medicine path or themotor base 49, a counting means (not shown) configured to counting the number of the medicines dispensed from thefeeder container 41 is provided. - The
counter device 185 can be operated in a plurality of operation modes including a counting mode or a predetermined quantity dispensing mode. The counting mode is a mode for counting the number of the medicines accommodated in thefeeder container 41 mounted on themotor base 40 by dispensing all themedicines 40 therein. Thecounter device 185 starts an operation according to the counting mode by pressing on thestart button 189 b when thefeeder container 41 is mounted on themotor base 40. Further, the number of medicines, which is counted by the counting means (not shown) provided in thecontainer attaching portion 187, is displayed in thedisplay 189 g. - The predetermined quantity dispensing mode is an operation mode for dispensing the medicine from the
feeder container 41 mounted on themotor base 40 by a quantity which a user inputs and sets through the tenkey pad 189 a. Thecounter device 185 operates in the predetermined quantity dispensing mode when the quantity of the medicines to be dispensed from the feeder container 41 (set quantity Q) is inputted through the tenkey pad 189 a and then thestart button 189 b is pressed on. After thecounter device 185 starts the operation according to the predetermined quantity dispensing mode, as the quantity of the dispensed medicines comes to the set quantity Q, the rotation of themotor 43 provided in themotor base 40 becomes slow to thereby reduce a dispensing speed of the medicines. In thecounter device 185 according to the present embodiment, when the quantity of the dispensed medicines becomes Q−2, the dispensing speed of the medicines is reduced. Thus, excessively dispensing the medicines by an error is prevented. - After the
counter device 185 operates in the above-described counting mode or the predetermined quantity dispensing mode, the operation information associated therewith can be written into thetag 49 provided in the bottom surface of thefeeder container 41 through the reader-writer 44 provided in themotor base 40 by the counter device. More specifically, after thecounter device 185 operates in the counting mode, if thewrite button 189 e provided in theoperation panel 189 is pressed on, then the counted number of the medicines is written into thetag 49. Further, after thecounter device 185 operates in the predetermined quantity dispensing mode, if thewrite button 189 e is pressed on, then the counted number of the medicines is written into thetag 49. Thus, in case thecounter device 185 counts the quantity of the medicines in thefeeder container 41 or counts and removes the medicines and the data associated therewith is written into thetag 49 and then thefeeder container 41 is set in themain storage part 20 or thesub storage part 120 of themedicine dispensing system 1, the data written into thetag 49 by thecounter device 185 can be effectively used to control themedicine dispensing system 1 or medicine management. More specifically, after the data is written in thetag 49 by thecounter device 185 as described above, if thefeeder container 41 is set in themain storage part 20 or thesub storage part 120 or thefeeder container 41 is fitted to therecess 117 b of thecontainer placing portion 117 a provided in theworktable 117, the data written into thetag 49 may be read through the reader-writer feeder container 41 in thecounter device 185 can be effectively used for the operation control of themedicine dispensing system 1 or the stock management of medicines. - The
counter device 185 is an example of the above-described device provided separately from themedicine dispensing system 1. Further, thecounter device 185 itself serves as a medicine dispensing device for dispensing medicines. That is, the counter device (medicine dispensing device) 185 includes thefeeder container 41 configured to store and dispense the medicines and a control means (not shown) configured to data-communicate with thetag 49 provided in thefeeder container 41. Thefeeder container 41 is configured to be attachable and detachable. Thecounter device 185 can perform data-communication of the data characteristic for thefeeder container 41 such as the quantity of the medicines in thefeeder container 41 with thetag 49 provided in thefeeder container 41 and the above-described control means. Accordingly, thecounter device 185 corresponds to a medicine dispensing device provided separately from themedicine dispensing system 1. - Further, as described above, the
medicine dispensing system 1 can read the information specifying the operator read from an employee card or an ID card, and easily and accurately record a person who performed the medicine supplement for thefeeder container 41 of eachcassette 32 into thetag 49 using such a data. It is illustrated in the above-described embodiment that the operator information is specified by items carried by the operator such as the employee card or the ID card or items assigned to each operator. However, the present invention should not be limited to such a configuration. For example, the operator information may be specified by a biometric certification such as a fingerprint. Further, the above-described embodiment employs a configuration wherein the operator information is read from any medium and the data for specifying the operator can be automatically inputted based on data associated therewith. However, the present invention should not be limited to such a configuration. - The operation mode of the
medicine dispensing system 1 is changed into the medicine filling mode upon a condition that thefeeder container 41 of thecassette 32 removed from themain storage part 20 or thesub storage part 120 is fitted to therecess 117 b of theworktable 117 and data communication becomes possible through the reader-writer 117 c between thetag 48 and the control means 170. That is, in themedicine dispensing system 1, it serves as a trigger for changing the operation mode to fit thefeeder container 41 to therecess 117 b of theworktable 117 and to enable the data-communication. Thus, according to themedicine dispensing system 1, when the operation mode is changed into the medicine filling mode, the operator does not need to perform complicated work. Further, it is illustrated in the above-described embodiment that the operation mode is changed by fitting thefeeder container 41 to therecess 117 b. However, the present invention should not be limited to such a configuration. - As described above, the
medicine dispensing system 1 is capable of reading the identification mark, which is assigned to each kind of medicine, such as the barcode written on the original medicine box by means of a mark reading means configured to read identification marks such as thebarcode reader 118 b. Further, the information on the kind of medicine specified as described above is recorded into thetag 49 by the data-communication between the control means 170 and thetag 49 provided in thefeeder container 41. Thus, themedicine dispensing system 1 does not need any effort such as an operator's manual input of the kind of medicines when themedicine dispensing system 1 operates in the medicine filling mode. Accordingly, the information on the kind of medicine can be more easily and accurately recorded into thetag 49. Further, it is illustrated in the above-described embodiment that the kind of the medicine is specified by reading the barcode assigned to each medicine by thebarcode reader 118 b and the data associated with such kind of medicine can be automatically inputted. However, the present invention should not be limited thereto. Further, thebarcode reader 118 b may read any barcodes including a one-dimensional barcode and a two-dimensional barcode. Further, it is illustrated in the above-described embodiment that thebarcode reader 118 b is capable of reading the barcode assigned to each kind of medicine. However, the present invention should not be limited to such a configuration. The present invention may employ an appropriate reader capable of reading a mark made by a color combination or reading the information recorded in an RFID tag instead of thebarcode reader 118 b. - As described above, in the
medicine dispensing system 1, only by positioning thefeeder container 41 in therecess 117 b of theworktable 117, the data-communication becomes possible without any contact through thebarcode reader 118 b provided in a position corresponding to therecess 117 b. Thus, in themedicine dispensing system 1, data-communication becomes possible between thetag 49 and the control means 170 without any effort, for example, such as connecting a wire to thefeeder container 41, and serial operations such as renewing, writing and managing the characteristic container information on eachfeeder container 41 can be smoothly performed. Further, in the above-described embodiment, the RFID tag or the RFID reader-writer is employed as thetag 49 or the reader-information into thetag 49 can be performed without any contact. However, the present invention should not be limited to such a configuration. That is, the information may be read and written by using other kinds of information, recordable medium or reader-writer. Also, although the data-communication is possible without any contact, the data-communication may be performed through wire connection. - In the
medicine dispensing system 1 according to the above-described embodiment, it is possible to read and write the data characteristic in eachfeeder container 41, which is recorded in thetag 49 provided in eachfeeder container 41. More specifically, the data such as the kind or quantity of the accommodated medicines and a name of an operator performing the medicine supplement. Thus, themedicine dispensing system 1 may be configured such that when thefeeder container 41 filled with medicines is attached to themotor base 40 appropriately selected from the plurality ofmotor bases 40 previously provided in themain storage part 20 of themain unit 2 and thesub storage part 120 of thesub unit 3, the control means 170 specifies where thefeeder container 41 accommodating the medicines required for packing and thus the medicines can be dispensed according to the kind and quantity corresponding to a prescription. That is, according to such a configuration, themedicine dispensing system 1 may be a device of a so-called free address type wherein thefeeder container 41 can be mounted in any position, not of a so-called fixed address type wherein the mount position of eachfeeder container 41 is fixed. - Further, the
medicine dispensing system 1 may be a device of a semi-fixed type wherein themotor base 40 configured to attach only thefeeder container 41 for accommodating medicines with a particular property thereon is specified. More specifically, themedicine dispensing system 1 may handle various kinds of the medicines. However, depending on the kind of medicines, there are medicines prone to bound, roll, break or chip due to a drop impact at a place where they are dispensed from thefeeder container 41. When dealing with the medicines with such properties (hereinafter, those medicines are referred to as specific medicines), a packing abnormality may occur unless a timing of packing the medicines is delayed until the medicines become stable without bounding or rolling or a means for buffering the drop impact is devised. - Preferably, the
feeder container 41 for accommodating the medicines (specific medicines) prone to bound, roll, break or chip as described above is to be attached in a lower position of themain storage part 20 and thesub storage part 120 or in a position where the above-described concerns can be resolved. Accordingly, in case of the above-described concerns, themedicine dispensing system 1 may be a device in the above-described semi-fixed address type. More specifically, in case the motor bases 40 are upwardly and downwardly provided in six stages in themain storage part 20 and thesub storage part 120 as shown inFIG. 51 , themedicine dispensing system 1 may regulate thefeeder container 41 accommodating the medicines with concerns of bounding or rolling (specific medicines) and may in some embodiments be attached to themotor base 40 in a region from a bottom portion up to two stages (hereinafter, this may be referred to as fixed address region Fi). - Further, the
medicine dispensing system 1 may regulate thefeeder container 41 accommodating the medicines except that the specific medicines may be attached not only in the fixed address region Fi but also to the motor bases 40 in a region (hereinafter, this may be referred to as a free address region Fr) other than the region Fi. Also, as for thefeeder container 41 which can be attached in the free address region Fr, its attachment arrangement may be regulated in a manner of subdividing into two or more groups. More specifically, as for thefeeder container 41 accommodating the medicines other than the specific medicines and inappropriate to drop from a higher place, it may be regulated that such afeeder container 41 is attached in a region lower than a free address region Fr1 divided into two stages above the fixed address region Fi. And, as for thefeeder container 41 accommodating the medicines with no concerns caused by dropping, it may be regulated that such afeeder container 41 is attached to themotor base 40 in a free address region Fr2 divided into two stages above the free address region Fr1. The above-described regulation for a correspondence relationship between thefeeder container 41 and themotor base 40 in each region is built in a control means 190 in a mariner of storing it in a memory means in the control means 190 as a container mounting database (correspondence relationship regulating part) 193 as shown inFIG. 52 . - As described above, in case the regions of installing a large number of the motor bases 40 provided in the
main storage part 20 or thesub storage part 120 are classified into a plurality of regions (container mounting region) such as the fixed address region Fi and the free address regions Fr (Fr1, Fr2) according to a height of the regions, the correspondence relationship between themotor base 40 and thefeeder container 41 may be regulated as a relationship with the container mounting region at a height which becomes an upper attachment limit of thefeeder container 41 determined depending on the kinds of the medicines accommodated in thisfeeder container 41. More specifically, the correspondence relationship between themotor base 40 and eachfeeder container 41 may be determined considering some or all of the following: a bound factor counted for a correlation between a drop height of the medicines accommodated in eachfeeder container 41 and a bound thereof; a rolling factor counted for a correlation between the drop height and the rolling; and a value of factor counted for a drop height wherein the breakage or chipping becomes equal to or less than a certain probability. - In the present embodiment, a correspondence label is attached on the
feeder container 41 and themotor base 40 such that an operator performing detachment of thefeeder container 41 can easily distinguish the regulations stored in the above-described container mounting database 193. More specifically, a specific label A colored in blue, for example, is attached on themotor base 40 in the fixed address region Fi and thefeeder container 41 accommodating the specific medicines. Further, a specific label B colored in green, for example, is attached on themotor base 40 in the free address region Fr1. Also, the label B is attached on thefeeder container 41 which may be attached in any of the free address region Fr1 and the fixed address region Fi. Likewise, a specific label C colored in white, for example, is attached on themotor base 40 in the free address region Fr1. Also, the label C is attached on thefeeder container 41 which may be attached in any of the free address regions Fr1 and Fr2 and the fixed address region Fi. Thus, the operator can be intuitively aware to attach thefeeder container 41 in a region with the same label as the label of thefeeder container 41 to be attached or in a region lower than said region. - As described above, when the
medicine dispensing system 1 is the device of the above-described semi-fixed address type, for example, the control means 190 shown inFIG. 52 may be employed instead of the above-described control means 170. Hereinafter, themedicine dispensing system 1 provided with the control means 190 will be explained focused on configurations and operations of the control means 190. Further, in the following description, in order to simplify the description, an example will be described wherein the region of themain storage part 20 or thesub storage part 120 is classified into two regions of the fixed address region Fi and the free address region Fr according to the height of themain storage part 20 or thesub storage part 120. - In addition to the function of the above-described control means 170, the control means 190 has a judging
part 191 having a function of performing an error judgment operation for confirming whether thefeeder container 41 to be set in themotor base 50 in the fixed address region Fi (hereinafter, this may be referred to as a specific feeder container 41 x) is mounted on thewrong motor base 40. That is, when thefeeder container 41 is attached to themotor base 40, the control means 190 allow the judgingpart 191 to perform the error judgment operation to thereby judge whether or not the attachedfeeder container 41 is the specific feeder container 41 x. Also, the control means allows the judging part to perform the error judgment operation for judging an erroneous mount by confirming whether the specific feeder container 41 x is erroneously mounted on themotor base 40 in the region other than the fixed address region Fi (hereinafter, this may be referred to as a free address region Fr). More specifically, in the free address region Fr1, divided into two stages above the fixed address region Fi, or in the free address region Fr2, divided into two stages above the free address region Fr1. Hereinafter, the error judgment operation will be described in detail. - (Error judgment operation) In the
medicine dispensing system 1 with the control means 190, when thefeeder container 41 is mounted on themotor base 40, the error judgment operation is performed according to a control flow shown inFIG. 53 . More specifically, if the erroneous mount judging operation begins, the judgingpart 191 confirms whether there is anyfeeder container 41 erroneously mounted against the regulation of the container mounting database 193 in Steps 1-1 to 1-3, based on the following: the above-described container mounting database 193; the region in which themotor base 40 with thefeeder container 41 mounted thereon exists; and the kind of the medicines read from thetag 49 of thefeeder container 41. - Even more specifically, first in Step 1-1, data-communication is performed between the control means 190 and the
tag 49 of thefeeder container 41 mounted on themotor base 40 by the reader-writer 44 provided in each of the motor bases 40 in themain storage part 20 or thesub storage part 120. Thus, the control means 190 specifies which region of the fixed address region Fi and the free address region Fr themotor base 40 with thefeeder container 41 mounted thereon exists. Further, in addition to the above, the control means 190 confirms whether or not thefeeder container 41 mounted on themotor base 40 is the specific feeder container 41 x. That is, whether or not the medicines in thefeeder container 41 are the specific medicines with the concerns of breakage or chipping. Then, the control flow proceeds to Step 1-2. - When the control flow proceeds to Step 1-2, the judging
part 191 of the control means 190 confirms whether or not the medicines accommodated in thefeeder container 41 confirmed in Step 1-1 are the specific medicines with the concerns of breakage or chipping. In this case, if the medicines are not the specific medicines, thefeeder container 41 accommodating those medicines may be mounted on themotor base 40 in any of the fixed address region Fi and the free address region Fr. Thus, when it is checked in Step 1-2 that the kind of medicines is not the specific medicine, the control flow proceeds to Step 1-6 and it is judged that thefeeder container 41 is mounted in a normal position (right mount state). Then, the control flow is ended. - Meanwhile, when it is checked in Step 1-2 that the medicines accommodated in the
feeder container 41 provided in themain storage part 20 or thesub storage part 120 are the specific medicines, the control flow proceeds to Step 1-3. It is checked in Step 1-3 whether themotor base 40 provided with thefeeder container 41 is in the fixed address region Fi of themain storage part 20 or thesub storage part 120. In this case, when thefeeder container 41 is mounted on themotor base 40 in the fixed address region Fi, it is assumed that when the medicines in the feeder container 41 (the specific medicines) are dispensed, no problems due to the bound or breakage occurs. Accordingly, in this case, the control flow proceeds to Step 1-6 and it is judged that thefeeder container 41 is mounted on the normal position. Then, the control flow is ended. - Meanwhile, when it is checked in Step 1-3 that the
motor base 40 provided with thefeeder container 41 is not in the fixed address region Fi but in the free address region Fr, there are concerns about the problems due to the bound or breakage by dispensing the medicines (the specific medicines) from thisfeeder container 41. Accordingly, in this case, the control flow proceeds to Step 1-4 and it is judged as the erroneous mount state that thefeeder container 41 is not mounted in the normal position. Then, the control flow proceeds to Step 1-5 to perform a display for warning the erroneous mount state in theoperating panel 118 a provided in the front surface of the main body of themain unit 2 and the control flow is ended. - In the
medicine dispensing system 1 provided with the control means 190, a medicine packing operation under the general operation mode can be performed according to the control flow shown inFIG. 54 using judgment results from the above-described error judgment operation. Hereinafter, the packing operation under the general operation mode, which is performed using the judgment results from the error judgment operation, will be described. - (Packing operation using the judgment results from the error judgment operation) According to the
medicine dispensing system 1 provided with the control means 190, if a prescription data for designating the kind, the quantity and the number of packs of the medicines to be packed is inputted to the control means 190, an operation under the general operation mode is started. If the operation under the general operation mode is started, the mounting state of thefeeder container 41 for themotor base 40 provided in the drums of themain storage part 20 and thesub storage part 120 is confirmed in Step 2-1. Then, if the control flow proceeds to Step 2-2, it is checked whether thefeeder container 41 accommodating the medicines to be packed according to the previously-inputted prescription data (hereinafter, this may be referred to as a packing feeder container 41 y) is mounted on themain storage part 20 or thesub storage part 120. In this case, when the packing feeder containers 41 y is empty, the control flow proceeds to Step 2-7 and an information indicating an error (a feeder container insertion error) is displayed in theoperating panel 118 a as shown inFIG. 55 . Further, in Step 2-7, the packing operation is stopped. Then, the control flow proceeds to Step 2-6 which will be described below. - Meanwhile, when all the packing feeder containers 41 y are mounted in Step 2-2, the control flow proceeds to Step 2-3. It is checked in Step 2-3 according to the above-described control flow shown in
FIG. 53 whether not only the packing feeder container 41 y but also all thefeeder containers 41 mounted on themain storage part 20 and thesub storage part 120 are erroneously mounted. When the erroneous mounting is confirmed in Step 2-3, that is, when it is confirmed in Step 2-3 that the feeder container 41 (the specific feeder container 41 x) accommodating the specific medicines having problems such as bound or breakage, which should be originally mounted in the fixed address region Fi, is mounted in the free address region Fr in themain storage part 20 or thesub storage part 120, the control flow proceeds to Step 2-8. - It is checked in Step 2-8 whether the erroneously-mounted
feeder container 41 is a feeder container accommodating the medicines to be packed (the packing feeder container 41 y). In this case, when the erroneously-mountedfeeder container 41 corresponds to the packing feeder container 41 y, continuing to dispense the medicines as it is can cause the problems such as packing abnormality resulting from bound or rolling of the medicines in the place where the medicines are dispensed or breakage and chipping of the medicines. Accordingly, in this case, the control flow proceeds to Step 2-10 and information indicating an error (a feeder container erroneous mounting error) purporting that the feeder container 41 (the specific feeder container 41 x) is erroneously mounted in the free address region Fr is displayed in theoperating panel 118 a. Also, the packing operation is stopped until the erroneously-mountedfeeder container 41 is mounted in the fixed address region Fi. - Meanwhile, when it is judged in Step 2-8 that the erroneously-mounted
feeder container 41 does not correspond to the packing feeder container 41 y, the medicines are not allowed to be dispensed from the erroneously-mountedfeeder container 41 in the packing operation. Thus, although the packing operation continues as thefeeder container 41 to be mounted in the fixed address region Fi is erroneously mounted, it is assumed that there is no problem due to the above-described bound, rolling, breakage and chipping of the medicines. Accordingly, in this case, a message for urging to resolve the erroneous mounting (an erroneous mounting resolving urging message) as shown inFIG. 56 is displayed in Step 2-9. Then, the control flow proceeds to Step 2-4 and the packing operation continues as the erroneous mounting resolving urging message is displayed in theoperating panel 118 a in Step 2-9. - When it is judged in Step 2-3 that no
feeder container 41 is erroneously mounted, or when it is judged in Step 2-8 that the erroneously-mountedfeeder container 41 does not correspond to the packing feeder container 41 y, the control flow proceeds to Step 2-4. It is checked in Step 2-4 whether the packing feeder container 41 y accommodating the medicines to be packed is pulled out while the control flow proceeds from said Step 2-1. In this case, when it is confirmed that the packing feed container 41 y is pulled out, the control flow proceeds to Step 2-11 and an information indicating an error to this effect (a feeder container identification error) is displayed in theoperating panel 118 a as shown inFIG. 58 . Also, the packing operation is stopped until the pulled-out packing feeder container 41 y is mounted again. Meanwhile, when it is judged that the packing feeder container 41 y is not pulled out, the control flow proceeds to Step 2-5 and the packing operation is performed. Then, the control flow proceeds to Step 2-6 and it is checked whether all the medicines to be packed according to the prescription data inputted at the time of starting the medicine packing operation under the general operation mode are packed. In this case, when packing the medicines to be packed according to the prescription data is not completed, the control flow returns to Step 2-2. Meanwhile, when packing all the medicines is completed, the control flow is ended. - As described above, in case the
medicine dispensing system 1 employs the control means 190, the error judgment operation is performed according to the control flow shown inFIG. 53 and therefore it can be judged whether thefeeder container 41 is erroneously mounted in the container mounting part where thefeeder container 41 should not be mounted originally. Further, as shown in the control flow ofFIG. 54 , in themedicine dispensing system 1, when thefeeder container 41 is erroneously mounted and such an erroneously-mountedfeeder container 41 does not correspond to the feeder container accommodating the medicines to be packed (the packing feeder container 41 y), dispensing the medicines continues due to no inconvenience in packing the medicines. Thus, the work efficiency in dispensing and packing the medicines is enhanced. Meanwhile, when the erroneously-mounted packing feeder container 41 y accommodates the above-described medicines with the concerns of problems such as bound or breakage, dispensing and packing the medicine is stopped. Thus, where themedicine dispensing system 1 is configured as described above, although there is the erroneously-mountedfeeder container 41, the packing abnormality caused by the problems such as bound or breakage of the medicines can be prevented while minimizing a loss in work efficiency. - In an example illustrated in the above-described embodiment, the motor bases 40 capable of mounting the
feeder container 41 thereon are provided as divided into multiple stages in an upward and downward direction. Further, the motor bases are regulated in a two-stage region (the container mounting region) of the fixed address region Fi and the free address region Fr according to the height. Further, the corresponding relationship between themotor base 40 and thefeeder container 41 to be attached thereto is regulated in the container mounting database 193 as the relationship with the container mounting region being at the height which becomes the upper attachment limit of thefeeder container 41 determined according to the kinds of medicines. That is, a region which becomes the upper attachment limit of thefeeder container 41 accommodating the specific medicines causing the problems such as bound or breakage is regulated as the fixed address region Fi. Further, a region which becomes the upper attachment limit of thefeeder container 41 accommodating the medicines causing less problems such as bound or breakage is regulated as the free address region Fr. - However, the regulation (classification) for the relationship with the container mounting region being at the height which becomes the upper attachment limit of the
feeder container 41 regulated in the container mounting database 193 should not be limited to the above-described. The region divided into multiple stages in an upward and downward direction where the motor bases 40 are provided may be regulated to be divided into still more stages according to the height. More specifically, the regions may be classified into three stages by classifying the free address region Fr into two regions Fr1, Fr2 as described above or may be classified into still more stages. In this case, the medicine dispensing system is configured such that the correspondence relationship between themotor base 40 and thefeeder container 41 to be attached thereto is regulated in the container mounting database 193 as the relationship with the region (container mounting region) being at the height which becomes the upper attachment limit of a medicine feeding container determined according to the kinds of the medicines, and that it is judged as an erroneous mount state by the error judgment operation when thefeeder container 41 is mounted on themotor base 40 in the container mounting region positioned above the container mounting region being at the height which becomes the upper attachment limit, and that it is judged as a right mount state by the error judgment operation when thefeeder container 41 is mounted on themotor base 40 in the container mounting region being at the height equal to or less than said upper attachment limit. Accordingly, the attachment state of thefeeder container 41 can be managed in more detail. - The height (the container mounting region) which becomes the upper attachment limit of the
feeder container 41 may be previously determined based on the factors counted for the bound, rolling, breakage and chipping of the medicines due to drop of the medicines per each kind of the medicines or the classification of the medicines in each grade. The height (the container mounting region) which becomes the upper attachment limit may be determined by the control means 190 in an orderly manner according to the factor or grade. - The above-described
medicine dispensing system 1 may include asearch part 192 having a searching function of searching and selecting themotor base 40 which must mount thefeeder container 41 judged as the erroneous mount by the error judgment operation of the control means 190, as shown by a two-dot chain line inFIG. 52 . More specifically, a search condition may be determined by reading the information recorded in thetag 49 through the data-communication between thetag 49 provided in thefeeder container 41 and the reader-writer 117 c by removing thefeeder container 41 judged as the erroneous mount by the error judgment operation and fitting the feeder container to therecess 117 b provided in theworktable 117 of themain unit 2. And, themotor base 40 suitable for mounting thefeeder container 41 may be searched and selected by thesearch part 192. Further, as for the search condition, it is preferred to appropriately display the search condition in theoperating panel 118 a as shown inFIG. 59 . Meanwhile, instead of determining the searching condition by reading the information of the erroneously-mountedfeeder container 41 through the data-communication between thetag 49 and the reader-writer 117 c, an operator may manually input the search condition through theoperating panel 118 a and thesearch part 192 may search the motor base based on the manually inputted search condition. In this case, for example, the search condition can be appropriately inputted by displaying a search condition determining screen shown inFIG. 59 in theoperating panel 118 a. - Further, when the position of the
motor base 40 suitable for mounting the erroneously-mountedfeeder container 41 is searched as described above, themain storage part 20 or thesub storage part 120 may be operated such that the selectedmotor base 40 comes to a position where an operator can perform the attachment/detachment work of the feeder container 41 (an attachment/detachment work position). According to such a configuration, the attachment/detachment work for the erroneously-mountedfeeder container 41 becomes still easier. - As described above, in the present embodiment, the
medicine dispensing system 1 is constructed by combining themain unit 2 and thesub unit 3 and a large number of thecassettes 32 are provided not only in themain storage part 20 but also in thesub storage part 120. Thus, when constructing themedicine dispensing system 1, it is preferred to read, write or manage the characteristic container information on thefeeder container 41 of each of thecassettes 32 as described in the foregoing embodiment. Further, it is illustrated in the above-described embodiment that themedicine dispensing system 1 is constructed by combining themain unit 2 and thesub unit 3. However, the present invention should not be limited to such a configuration. The characteristic container information can be accurately read, written or managed when only a part corresponding to themain unit 2 is utilized as the medicine dispensing system. - In the
medicine dispensing system 1, thesub unit 3 does not need themedicine packing part 21. Thus, themedicine dispensing system 1 can reduce the device configuration and minimize an installation area, when compared to a case of providing a plurality of equivalents of the medicine packing part to themain unit 2. Further, according to the configuration of themedicine dispensing system 1, a part corresponding to themedicine packing part 21 can be omitted in thesub unit 3 and thus thesub unit 3 can be configured to accommodate various kinds of medicines in a large quantity. Further, since thesub unit 3 does not need themedicine packing part 21, themedicine dispensing system 1 can simplify a device configuration or minimize efforts for maintenance. - Since the
transfer device 5 employed in themedicine dispensing system 1 has thepipe line 140 for transferring the medicines and is configured to suck the medicines inputted therein, the medicines dispensed in thesub unit 3 can be smoothly conveyed toward themain unit 2. Further, since thetransfer device 5 is configured to suck and convey the medicines, the medicines can be conveyed along any conveying path by appropriately curving thepipe line 140. Thus, themedicine dispensing system 1 has a high degree of freedom in a device configuration and layout of themain unit 2 and thesub unit 3. - Further, the above-described
transfer device 5 is configured to suck and transfer the medicines inputted in themeasures 145 of themedicine receiving part 142 connected to thepipe line 140 toward themedicine dispensing part 143. However, the present invention should not be limited to such a configuration. Thetransfer device 5 may be configured to pressure-transfer the medicines from themedicine receiving part 142 toward themedicine dispensing part 143. Further, thetransfer device 5 includes thepipe line 140 of one channel. However, the present invention should not be limited to such a configuration. The conveying path of many channels includingmany pipe lines 140 may be employed. - In the
medicine dispensing system 1 of the present embodiment, thetag 49 is provided in each of thecassettes 32 set in themain storage part 20 and thesub storage part 120. Also, the data can be transmitted to and received from thetag 49 and the data can be renewed or written in the tag by the reader-writer 117 c provided in theworktable 117. Thus, themedicine dispensing system 1 can record various data such as data on the kind or quantity of the medicines accommodated in eachcassette 32, data on a supplement history related to a person performing a medicine supplement in eachcassette 41 and date and time of the medicine supplement, data on a usage history of each cassette, and the like into thetag 49. Further, the medicines accommodated in eachcassette 32 can be managed or the user can be notified of a maintenance time of eachcassette 32 based on the data recorded in thetag 49. - Further, it is illustrated in the above-described embodiment that the
tag 49 is provided in thefeeder container 41 of eachcassette 32 and the reader-writers worktable 117. However, the present invention should not be limited to such a configuration. That is, themedicine dispensing system 1 may be configured such that all thecassettes 32 do not have thetag 49 and some or all of the motor bases 49 do not have the reader-writers 44. Likewise, themedicine dispensing system 1 may not include the reader-writer 117 c. Further, themedicine dispensing system 1 may be configured such that only somecassettes 32, for example, for managing the quantity of the medicines include thetag 49. - As described above, the
feeder container 41 of thecassette 32 can adjust the size of the opening 47 for dispensing the medicines according to the size of the medicines to be accommodated by appropriately replacing theopening attachment 41 b. Also, therotor 48 of thefeeder container 41 can be appropriately replaced with another one having agroove 48 a sized to be suitable for the size of the medicines to be accommodated. Thus, thecassette 32 can deal with the medicines of various sizes by appropriately replacing theopening attachment 41 b or therotor 48. - Further, it is illustrated in the above-described embodiment that the
opening attachment 41 b or therotor 48 can be appropriately replaced in thefeeder container 41 according to the size of the medicines. However, the present invention should not be limited to such a configuration. More specifically, the opening 47 a of a fixed size may be formed in thefeeder container 41 or therotor 48 may not be replaceable. - Also, in the
medicine dispensing system 1, considering that the packingpaper sheet 98 with the length corresponding to n packs of the medicine pack (three packs in the present embodiment) exists between thepack forming mechanism 96 and theprinting part 99, the information on the medicines is printed by theprinting part 99 at a time (time Z) as early as the time period (time period Y) required to rotate thesection forming body 81 as much as a quantity corresponding ton sections 81 a (three sections in the present embodiment) from the timing (timing X) when the medicines are dispensed through theopening 82 c from thesection 81 a in themedicine preparing part 80. Further, at a time before the timing Z of printing to the packingpaper sheet 98, the medicines dispensed from themain storage part 20 or thesub storage part 120 are inputted in thesection 81 a. That is, printing to the packingpaper sheet 98 is performed in themedicine dispensing system 1 upon a condition that the medicines are dispensed from themain storage part 20,sub storage part 120 and themanual dispensing unit 23 to themedicine preparing part 80. Thus, when a dispensing abnormality of the medicines to themedicine preparing part 80 occurs, printing to the packingpaper sheet 98 is not performed. Thus, themedicine dispensing part 1 can easily and accurately monitor whether a dispensing abnormality of the medicines from themain storage part 20, thesub storage part 120 and themanual dispensing unit 23 to themedicine preparing part 80, only by checking whether or not printing to the packingpaper sheet 98 is performed. Further, according to the above-described configuration, when the medicines to be packed into the packingpaper sheet 98 lack or do not exist, unnecessary printing is not performed to the packingpaper sheet 98 and a waste of the packingpaper sheet 98 to that extent can be prevented. - In the above-described embodiment, at the timing before the timing Z, the medicines are dispensed from all of the
main storage part 20, thestorage part 120 and themanual dispensing unit 23, which constitute the medicine dispensing means, and inputted in eachsection 81 a. However, the present invention should not be limited to such a configuration. More specifically, the medicines dispensed from some of themain storage part 20, thesub storage part 120 and themanual dispensing unit 23, which constitute the medicine dispensing means, are dispensed into eachsection 81 a at a time after the time Z. Even more specifically, for example, since themanual dispensing unit 23 is installed in order to pack the medicines inputted by the user's own hands, it is considered that abnormality in inputting the medicines from themanual dispensing unit 23 to eachsection 81 a hardly occurs. Thus, in the aforementioned circumstance, the time of dispensing the medicines may be after the time Z with regard to some of parts constituting the medicine dispensing means. - The
medicine dispensing system 1 according to the above-described embodiment includes the circularsection forming body 81 with a plurality of the circumferentially-arrangedsections 81 a in themedicine preparing part 80 and is configured to dispense the medicines from each of thesections 81 a by relatively rotating thesection forming body 81 relative to theopening 82 c. Thus, according to the above-described configuration, a space required for operating thesection forming body 81 becomes minimized and thus the device configuration can be reduced. Further, themedicine preparing part 80 should not be limited to the above-described embodiment. For example, the medicine preparing part may be configured such that thesection forming body 81 has a plurality of linearly-arrangedsections 81 a and the medicines are dispensed from each of thesections 81 a one after another by linearly moving thesection forming body 81 relative to theopening 82 c. - Further, as described above, the
medicine dispensing system 1 has the set abnormality detecting means 38 at themain unit 2 or thesub unit 3. The set abnormality detecting means 38 is not the same as the conventionally known optical sensor but employs a so-called mechanical configuration wherein theswitch 38 b is turned on when thecassette 32 bumps against thecontact plate 38 a along with the rotation of thedrum 31 and thecontact plate 38 a swings thereby. Thus, according to the above-described set abnormality detecting means 38, the attachment abnormality of thecassette 32 can be accurately detected without an effect from a dust, when compared to a case of employing the optical sensor. - Also, it is illustrated that the
medicine dispensing system 1 includes the set abnormality detecting means 38 of a mechanical type at both themain unit 2 and thesub unit 3. However, the present invention should not be limited to such a configuration. The set abnormality detecting means 38 may be provided at one side or the set abnormality detecting means 38 and known detecting means such as an optical sensor may be used together. - In the
medicine dispensing system 1, theabnormality detecting mechanism 115 is provided in the conveying means 21 b of themedicine packing part 21 and the transfer abnormality of the packing paper sheet such as a paper jam of the packingpaper sheet 98 can be detected by theabnormality detecting mechanism 115. That is, theabnormality detecting mechanism 115 illustrated in the above-described embodiment has apinch roller 115 b rotatable independently of the conveying means 21 b and a paper transfer abnormality can be detected based on whether the rotation of thispinch roller 115 b is detected by therotary encoder 115 d during operation of the conveying means 21 b. Thus, themedicine dispensing system 1 of the present invention can minimize the waste of the packingpaper sheet 98 or the medicines due to the transfer abnormality of the packingpaper sheet 98. Further, it is illustrated in the above-described embodiment that theabnormality detecting mechanism 115 is positioned in thestraight portion 105 b of thecasing 105, which constitutes the conveying means 21 b, and in a position upstream in the transfer direction of the packingpaper sheet 98 in order to detect the transfer abnormality of the packing paper sheet in themedicine packing part 21 as fast as possible. However, the present invention should not be limited to such a configuration. Theabnormality detecting mechanism 115 may be positioned in a position further downstream than the aforementioned position. - In the above-described embodiment, the
medicine packing part 21 can appropriately bend thebent portion 105 c positioned at the distal end portion of thecasing 105, which constitutes the conveying means 21 b, relative to thestraight portion 105 b. Thus, in themedicine dispensing system 1, the packingpaper sheet 98 with the packed medicines can be removed from a better one of the dispensingopenings main unit 2. Further, the conveyingmeans 21 is configured to appropriately bend thebent portion 105 c. However, the conveying means may not have a part corresponding to thebent portion 105 c. Also, it is illustrated in the above-described embodiment that themedicine dispensing system 1 is constructed by combining themain unit 2 and thesub unit 3. However, the present invention should not be limited to such a configuration. Themain unit 2 may be used alone. - The above-described
medicine dispensing system 1 may be configured such that thetransfer device 5 is separately provided in addition to themain unit 2 and thesub unit 3 and the transfer device lies across the main and sub units. However, thetransfer device 5 may be previously assembled with thesub unit 3 and, when necessary, the same may be connected to themain unit 2 to provide extension of installation. That is, thesub unit 3 may or may not include thetransfer device 5 as a part of its configuration. - The
transfer device 5 of a type of sucking and transferring the medicines dispensed in thesub unit 3 is illustrated in the above-described embodiment. However, the present invention should not be limited to such a configuration. For example, atransfer device 210 shown inFIG. 25 may be employed. - More specifically, the
transfer device 210 is mainly comprised of asupport part 220 and adrive part 230. As shown inFIG. 25 , thesupport part 220 has a supportingshaft 221 and abase part 222. A supportingshaft 221 has aflange 223 provided at one end and can be erected approximately upright by screw-fixing theflange 223. Thebase part 222 serves as a turning means for turning thedrive part 230 and is provided at the other end of the supportingshaft 221. Thebase part 222 includes aturn drive motor 225, aturn drive gear 226, and aseat plate 227. As shown inFIG. 25 , theseat plate 227 is a plate body that is horizontal when the supportingshaft 221 is erected. Further, theturn drive motor 225 is positioned such that its rotating shaft approximately vertically passes through theseat plate 227 from a lower surface thereof. Theturn drive gear 226 is connected to the rotating shaft of theturn drive motor 225 on an upper surface of theseat plate 227. - As shown in
FIG. 25 , thedrive part 230 includes two sets of medicine delivering units 231 (medicine delivering part) and a supportingplate 232 supporting them at their lower sides. Further, a turningshaft 234 is erected at an approximate center of the supportingplate 232. The turningshaft 234 approximately vertically extends from the supportingplate 232 and is rotatably supported on theseat plate 227 of thebase part 222 at its lower end. The turn drivengear 234 a is integrally coupled to the lower end of the turningshaft 234. The turn drivengear 234 a is meshed with theturn drive gear 226 of thebase part 222. Thus, as theturn drive motor 225 provided in thebase part 222 operates, the supportingplate 232 and themedicine delivering unit 231 provided thereon can turn integrally about the turningshaft 234. - Both of the
medicine delivering units medicine delivering unit 231 includes aslide base 235 and first and second slidingbodies 236, 237 (first and second sliding portions). Theslide base 235 and the first and second slidingbodies slide base 235 is fixed on theseat plate 227 of thebase part 222. In the present embodiment, as shown inFIG. 25 , the slidingbases medicine delivering units seat plate 227 and are arranged approximately parallel to each other. - As shown in
FIGS. 25 to 28 , the first slidingbody 236 is mounted on and covers theslide base 235 and is slidable in a lengthwise direction of theslide base 235. Further, the second slidingbody 237 is mounted on and covers the first slidingbody 236 and is slidable in a lengthwise direction of the first slidingbody 236. Thus, as themedicine delivering unit 231 is drawn out away from the slidingbase 235 by sliding the first slidingbody 236 and the second slidingbody 237 from theslide base 235 one after the other in a lengthwise direction, the medicine delivering unit can be expanded up to its overall length as shown inFIGS. 25 to 27 . Further, as each of the first and the second slidingbodies slide base 235 from the expanded state shown inFIGS. 25 to 27 , the medicine delivering unit decreases in its overall length and can be contracted to the extent of a length of theslide base 235. - More specifically, as shown in
FIG. 29 , theslide base 235 has the following: atop portion 235 a;side portions top portion 235 a in a widthwise direction thereof; and abottom portion side portions top portion 235 a. Theside portions top portion 235 a and thebottom portion 235 c, and are linearly beveled outwardly in a widthwise direction from thetop portion 235 a toward thebottom portion 235 c. Each of theside portions guide roller 235 d rotatable about a shaft which is approximately vertically erected on theside portion 235 b. - As shown in
FIG. 29 (b), theslide base 235 has adrive motor 235 e at a back side of thetop portion 235 a (below the top portion). Apulley 235 f is coupled to a rotating shaft of thedrive motor 235 e. Further, adrive pulley 235 h is coupled to one end of ashaft 235 g, which is approximately vertical to thetop portion 235 a, at the back side of thetop portion 235 a and in a position corresponding to one end of theslide base 235 in its lengthwise direction (hereinafter, this may be referred to as a leading end, if necessary). Thedrive pulley 235 h and theshaft 235 f rotate integrally by power from thedrive motor 235 e transferred through a drive belt 253 i wound between the drive pulley and thepulley 235 f. Further, theshaft 235 g approximately vertically passes through thetop portion 235 a of theslide base 235. As shown inFIG. 29 (a), adrive gear 235 j is coupled to the other end of theshaft 235 g (i.e. a portion protruding on a top surface of thetop portion 235 a). Thus, as thedrive motor 235 e operates, thedrive gear 235 j rotates about theshaft 235 g by the rotational power of thedrive motor 235 e. - The
slide base 235 has a belt fixing member positioned at the leading end of thetop portion 235 a and near one of theside portions 235 b. Thebelt fixing member 235 k is erected on a surface of thetop portion 235 a (on the top portion) and is fixed to engage atiming belt 248 which is described in detail below. - As shown in
FIG. 30 , the first slidingbody 236 is configured such that aguide rail 238, a drivenrack gear 241,pulleys slide member 244 and aguide roller 245 are assembled to amain body 239. Specifically, themain body 239 has atop portion 236 a andside portions top portion 236 a has an elongated and flat plate shape and theside portions top portion 236 a in a widthwise direction thereof. Theside portions top portion 236 a and are linearly beveled outwardly in the widthwise direction as being away from thetop portion 235 a. That is, theside portions top portion 236 a. Thetop portion 236 is provided with anopening 236 d extending in a lengthwise direction of themain body 239. -
Guide rails side portions side portion FIG. 28 , guiderollers side portions slide base 235 are fitted to theguide rails guide rollers guide rails FIGS. 28 and 30 , a drivenrack gear 241 is provided throughout an entire length of theside portion 236 b in the inside of theside portion 236 b above the guide rail 238 (near thetop portion 236 a). As shown inFIGS. 26 and 28 , when themedic delivering unit 231 is assembled, the drivenrack gear 241 is meshed with thedrive gear 235 j provided in thetop portion 235 a of theslide base 235. - Meanwhile, in the first sliding
body 236,pulley brackets side portion 236 c above the guide rail 238 (near thetop portion 236 a).Pulleys pulley bracket 246 is positioned near one end of the first sliding body 236 (hereinafter, this may be referred to as a leading end, if necessary), while thepulley bracket 247 is positioned near the other end thereof (hereinafter, this may be referred to as a base end, if necessary). Thepulleys top portion 236 a and fixed to thepulley brackets timing belt 248 is wound between thepulleys FIG. 26 , thetiming belt 248 is fitted and fixed to thebelt fixing member 235 k provided on theslide base 235. - The
slide member 244 has abelt fixing portion 244 a and a slidingbody fixing portion 244 b. Theslide member 244 is fixed to thetiming belt 248 by fitting thetiming belt 248 to thebelt fixing portion 244 a. Further, the slidingbody fixing portion 244 b is exposed on theopening 236 d of the first slidingbody 236 toward the top surface of thetop portion 236 a (upwardly) and is linearly slidable along theopening 236 d in a lengthwise direction of the first slidingbody 236. The slidingbody fixing portion 244 b is fixed to atop portion 237 a of the second slidingbody 237, which will be described in detail, by screws and the like in one embodiment although other ways of affixing are possible. - The second sliding
body 237 is provided to deliver medicines. As shownFIGS. 26 and 27 , the second sliding body is disposed on and covers the first slidingbody 236. Theslide member 244 of the first slidingbody 236 is fixed to one end of the second slidingbody 237 in a lengthwise direction thereof (hereinafter, this may be referred to as a base end, if necessary) by screws and the like. Thus, the second slidingbody 237 is connected to the first slidingbody 236 via theslide member 244. - As shown in
FIGS. 28 and 31 , the second slidingbody 237 includesmedicine receiving portion 237 d in addition to thetop portion 237 a orside portions top portion 237 a is a portion having an elongated flat plate shape and theside portions top portion 237 a in a widthwise direction. Theside portions side portions top portion 236 a and middle portion of theside portions top portion 236 a.Guide rails body 237. As shown inFIG. 28 , theguide rollers side portions body 236 are fitted to theguide rails body 237 can be relatively moved in the lengthwise direction of the first slidingbody 236. Further, as described above, the second slidingbody 237 is connected to the first slidingbody 236 via theslide member 244. Thus, the second slidingbody 237 is linearly moved relative to the first slidingbody 236 along with sliding movement of theslide member 244. - The
medicine receiving portion 237 d is provided in one end of the second slidingbody 237 in a lengthwise direction thereof (hereinafter, this may be referred to as a leading end, if necessary). Themedicine receiving portion 237 d has a shape of a measure with its top opened at thetop portion 237 a. A bottom surface of themedicine receiving portion 237 d is blocked by ashutter 255. Theshutter 255 is provided so as to be slidable in a lengthwise direction of the second slidingbody 237. The medicines, which are received in themedicine receiving portion 237 d, can be dispensed downwardly by opening theshutter 255. - Next, operations of the
transfer device 210 will be described in detail. Thetransfer device 210 can turn each of themedicine delivering units 231 about the turningshaft 234 by operating theturn drive motor 225 provided on thesupport part 220. Further, by operating thedrive motor 235 e provided in each of themedicine delivering units 231, thetransfer device 210 can linearly expand theslide base 235 and the first and second slidingbodies FIG. 25 (a), or pull the first and second slidingbodies slide base 235 into an entirely contracted state (hereinafter, this state is referred to as a contracted state) as shown inFIG. 25 (b). - The operations of the
medicine delivering unit 231 accompanied by the operation of thedrive motor 235 e are described in detail. As shown inFIG. 25 (b), if thedrive motor 235 e operates in the contracted state, the power therefrom is transferred to the drivepulley 235 h by thedrive belt 235 i provided in the back side of thetop portion 235 a in theslide base 235 and thedrive pulley 235 h rotates together with theshaft 235 g. Thus, thedrive gear 235 j provided on the surface of thetop portion 235 a is rotated. When thetop portion 235 a is viewed downwardly, if thedrive gear 235 j rotates counterclockwise, then the drivenrack gear 241 of the first slidingbody 236 meshed with thedrive gear 235 j is linearly transferred from the base end of theslide base 235 toward the leading end. Thus, the first slidingbody 236 with the drivenrack gear 241 slides from the base end of theslide base 235 toward the leading end. - In this case, as described above, the
timing belt 248 wound between thepulleys body 236 is fixed to thebelt fixing member 235 k erected on thetop portion 235 a of theslide base 235. Further, since theslide member 244 is fixed to thetiming belt 248, theslide member 244 and thetiming belt 248 integrally operate. Further, when thetransfer device 210 is in the contracted state, theslide member 244 is positioned near the base end of the first sliding body 236 (i.e. near the pulley 242). Meanwhile, thebelt fixing member 235 k is positioned near the leading end of the first sliding body 236 (i.e. near the pulley 234). That is, thebelt fixing member 235 k and theslide member 244 are obliquely (diagonally) opposed to each other with the timing belt. 248 therebetween. Thus, if the first slidingbody 236 slides from the base end of theslide base 235 toward the leading end, then thepulley 242 approaches thebelt fixing member 235 k. Meanwhile, theslide member 244 moves toward the pulley 243 (i.e. toward the leading end of the first sliding body 236) along theopening 236 d provided in thetop portion 236 a of the first slidingbody 236, while opposed to thebelt fixing member 235 k with thetiming belt 248 therebetween. - If the
slide member 244 moves to the leading end of the first slidingbody 236, the second slidingbody 237 integrally provided with the first sliding body via theslide member 244 also slides to the leading end of the first slidingbody 236. Then, as shown inFIG. 26 , if theslide member 244 reaches the leading end (the pulley 243) of the first slidingbody 236, both the first and the second slidingbodies medicine delivering unit 231 is fully expanded in its lengthwise direction of (i.e. in the expanded state). - Meanwhile, when the first and second sliding
bodies slide base 235 from the expanded state shown inFIG. 26 to contract the overall length of the medicine delivering unit 231 (i.e. the contracted state), themedicine delivering unit 231 operates in reverse to the above-described operations. That is, in order to achieve the contracted state, thedrive motor 235 e operates such that its rotating shaft rotates in an opposite direction to the expanded state. Therefore, the power of thedrive motor 235 e is transmitted to thedrive gear 235 j by thetiming belt 248, thedrive pulley 235 h and theshaft 235 g. Thedrive gear 235 j rotates in an opposite direction to a rotating direction wherein themedicine delivering unit 231 becomes in the expanded state. That is, when thetop portion 235 a is viewed downwardly, thedrive gear 235 j rotates clockwise. Thus, the drivenrack gear 241 meshed with thedrive gear 235 j is linearly moved toward the base end of theslide base 235 and the first slidingbody 236 slides from the base end of theslide base 235 toward the leading end. - If the first sliding
body 236 slides as described above, thepulley 243 positioned at the leading end of the first slidingbody 236 approaches thebelt fixing member 235 k. Also, theslide member 244, which is obliquely opposed to thebelt fixing member 235 k with thetiming belt 248 therebetween, moves toward thepulley 242 positioned at the base end of the first slidingbody 236 along theopening 236 d provided in thetop portion 236 a of the first slidingbody 236. Thus, the second slidingbody 237 connected to the first slidingbody 236 via theslide member 244 also slides toward the base end of theslide base 235 along with the first slidingbody 236. Then, when theslide member 244 reaches the base end (the pulley 242) of the first slidingbody 236, both the first and second slidingbodies medicine delivering unit 231 is contracted in its lengthwise direction. - The
transfer device 210 is disposed at the boundary between themain unit 2 and thesub unit 3 like thetransfer device 5 employed in the foregoing embodiment. More specifically, as shown inFIG. 25 , thetransfer device 210 is positioned on the bottom surface of the housing constituting thesub unit 3 by screw-fixing theflange 223 thereto and adjacent to the communicatingopening 4 b provided in thewall surface 4 a forming a boundary between thesub unit 3 and themain unit 2. Thus, in thetransfer device 210, if themedicine delivering unit 231 is expanded when the lengthwise direction of themedicine delivering unit 231 is orthogonal to thewall surface 4 a as shown inFIG. 25 , the second slidingbody 237 in one of the medicine delivering units 231 (hereinafter, this may be referred to as a deliveringunit 231 a) protrudes beyond thewall surface 4 a toward themain unit 2. Further, the second-slidingbody 237 of the other of the medicine delivering units 231 (hereinafter, this may be referred to as a deliveringunit 231 b) protrudes in thesub unit 3 in a direction opposite the above-described direction of themedicine delivering unit 231 a. - If the second sliding
body 237 of themedicine delivering unit 231 a protrudes toward themain unit 2, thesub collecting hopper 87 connected to themedicine preparing part 80 of themain unit 2 is positioned under themedicine receiving portion 237 d provided in the second slidingbody 237. Thus, if theshutter 255 of themedicine delivering unit 231 positioned in themain unit 2 is opened in the state shown inFIG. 25 (a), the medicine received in themedicine receiving portion 237 d can be dispensed to themedicine preparing part 80 of themain unit 2. On the other hand, if the second slidingbody 237 of themedicine delivering unit 231 b protrudes in thesub unit 3, themedicine receiving portion 237 d is positioned just below thesub hopper 135 provided in thesub unit 3. Thus, if the medicines are dispensed from the submedicine standby part 130 in such a state, then the medicines are inputted to themedicine receiving portion 237 d. - Next, operations of a
medicine dispensing system 1 employing thetransfer device 210 will be described focusing on a medicine transferring sequence by thetransfer device 210. As described above in the foregoing embodiment, themedicine dispensing system 1 dispenses the medicines dispensed from themain storage part 20 or the manual distributingunit 23 according to the prescription to each of thesections 81 a of thesection forming body 81 provided in themedicine preparing part 80 one pack at a time. - When the medicines to be prescribed are in
sub unit 3, the medicines are dispensed from each of thecassettes 32 of thesub storage part 120 one pack at a time. The medicines dispensed from thesub storage part 120 are gathered in the submedicine standby part 130. Meanwhile, themedicine delivering units transfer device 210 go into an expanded state. Thus, themedicine receiving portion 237 d provided in the second slidingbody 237 of one of themedicine delivering units medicine delivering unit 231 b inFIG. 25 (a)) is positioned under thesub hopper 135. In this state, if the medicines are dispensed from submedicine standby part 130, the medicines for one pack dispensed from thesub storage part 120 are received in themedicine receiving portion 237 d. - If the medicines are inputted into the
medicine receiving portion 237 d, themedicine delivering unit FIG. 25 (b). Then, theturn drive gear 226 provided in thebase part 222 of thetransfer device 210 operates to turn themedicine delivering units shaft 234 by 180 degrees. Then, themedicine delivering units medicine delivering unit 231 b receiving the medicines from thesub unit 3 protrudes into themain unit 2 and thus themedicine receiving portion 237 d is positioned above thesub collecting hoper 87 of themain unit 2. Further, the second slidingbody 237 of the othermedicine delivering unit 231 a protrudes below thesub hopper 135 and is allowed to receive the next medicines for one pack. - If the
medicine delivering units sub unit 3 respectively as described above, then theshutter 255 provided in themedicine receiving portion 237 d of themedicine delivering unit 231 b is opened and the medicines received from thesub unit 3 are dispensed to each of thesections 81 a of thesection forming body 81 provided in themedicine preparing part 80. Meanwhile, medicines for one pack are inputted from the submedicine standby part 130 to themedicine receiving portion 237 d of themedicine delivering unit 231 a. - In case the
medicine dispensing system 1 employstransfer device 210, the medicine dispensed in thesub unit 3 can be transferred to themain unit 2 by repeatedly expanding themedicine delivering units transfer device 210 is employed, the medicines dispensed in thesub unit 3 can be transferred to themain unit 2 and can be packed at themedicine packing part 21 together with the medicines dispensed in themain unit 2, similarly to the case of employing thetransfer device 5. - As described above, since the
transfer device 210 can turn themedicine delivering unit 231 in the contracted state, a space necessary for turning themedicine delivering unit 231 can be minimized. Further, since thetransfer device 210 can expand themedicine delivering unit 231 into the expanded state, the medicines can be received or dispensed at a position apart from thetransfer device 210. Thus, when thetransfer device 210 is employed, the space inside themedicine dispensing system 1 can be effectively used and themedicine dispensing system 1 can be compactly configured. - The
medicine dispensing system 1 may employ the above-describedtransfer device transfer device 300 shown inFIGS. 32 to 35 . Thetransfer device 300 will be now described in detail with reference to the drawings. As shown inFIG. 33 , thetransfer device 300 has abase part 310 and a turn part 330 (conveyance part). Thebase part 310 has abase plate 311 having a flat plate shape and adrive unit 312. Thedrive unit 312 is provided at a back side of thebase plate 311. Thedrive unit 312 has adrive motor 313 and agear box 315 and serves as a direction adjusting means configured to adjust the direction of theturn part 330. - The
gear box 315, which is positioned at an approximate central portion of thebase plate 311, has aturn drive gear 316 and a turn drivengear 317 therein. Theturn drive gear 316 of thegear box 315 is fixed to a rotating shaft of thedrive motor 313. Further, the turn drivengear 316 is meshed with theturn drive gear 316. The turn drivengear 317 is fixed to a turningshaft 318 fixed to theturn part 330. Further, the turningshaft 318 is erected on an approximately central portion of thebase part 311 while being rotatably supported thereon. Thus, as theturn motor 313 operates to rotate, theturn drive gear 316, the turn drivengear 317, the turningshaft 318 and theturn part 330 rotate together. - The
base plate 311 has adispensing opening 320 at its approximate center portion in its widthwise direction and at its one end in its lengthwise direction. Further, acontact member 321 is provided on a surface of thebase plate 311 in a position corresponding to thedispensing opening 320. Thecontact member 321 has anopening 322 communicating with the dispensingopening 320. Further, as shown inFIG. 32 , a pair ofguide rails base plate 311 with a predetermined gap therebetween. The guide rails 323, 323 are curved members having a circular arc shape with a predetermined curvature. Thus, agroove 325 is formed between theguide rails FIG. 32 ). - Meanwhile, as shown in
FIG. 32 , theturn part 330 has acover 331 which has a rectangular shape in a plan view. Further, as shown inFIG. 33 , component members of theturn part 330 includingmedicine containers 340, 340 (medicine delivery container) are accommodated inside thecover 331. More specifically, thecover 331 is opened at its bottom side and is disposed above thebase part 310. A receivingopening 331 d is provided in atop surface 331 a of the cover at one end of the cover in a lengthwise direction thereof. Thecover 331 is disposed above thebase plate 311 in such a manner that one end of the cover with the receivingopening 331 d is opposite the dispensingopening 320 provided in thebase plate 111 in the lengthwise direction of thetop surface 331 a and thetop surface 331 a is approximately parallel to thebase plate 311. - The turning
shaft 318 is integrally provided in thecover 331 at the approximately central portion of thetop surface 331 a. The turningshaft 318 is erected from thetop surface 331 a of thecover 331 and protrudes downward. The turningshaft 318 passes through an approximate center portion of thebase plate 311 and extends into thegear box 315 provided in the back side of thebase plate 311. The turning shaft is rotatably supported relative to thebase plate 311. The turn drivengear 317 is coupled to the turningshaft 318 in thegear box 315. Thus, as thedrive motor 313 operates to rotate theturn drive gear 316, the power therefrom rotates the turn drivengear 317 and the turningshaft 318 together and thus theturn part 330 including thecover 331 turns about the turningshaft 318. - As shown in
FIG. 33 ,guide rails shaft 318. Further, as shown inFIG. 32 , theguide rails cover 331. The turningshaft 318 is fitted between theguide rails guide rails member 334 fixed to the middle portion of the turningshaft 318. Accordingly, theguide rails shaft 318 and can rotate about the turningshaft 318. - Further,
guide rails cover 331 to linearly extend atlong sides cover 331. The guide rails 333, 333 are opposite theguide rails opposite guide rails medicine containers - As shown in
FIG. 32 , timing pulleys 335, 336 are coupled to both ends of thecover 331 in a lengthwise direction thereof and at an approximate middle portion of thecover 331 in a widthwise direction thereof. The timing pulleys 335, 336 are provided adjacent to both ends of theguide rail 332 in the lengthwise direction thereof. Each of the timing pulleys 335, 336 can rotate freely about respective shafts, which are approximately vertical to thetop surface 331 a. Atiming belt 337 is wound between the timing pulleys 335, 336. - The
medicine container 340 is a box-shaped member with an opening at its top surface. As shown inFIG. 33 , ashutter 342 is provided at a bottom surface of themedicine container 340. The medicines accommodated in themedicine container 340 can be dispensed downward when theshutter 342 is opened. Theshutter 342 can be opened when acontact portion 342 a is pressed and slid in a lengthwise direction of themedicine container 340. Theshutter 342 is biased in a direction of closing the bottom of themedicine container 340 at normal times to thereby block the bottom of the medicine container. In thecover 331, themedicine container 340 is positioned between a pair of theguide rails cover 331 relative to the turningshaft 318. - More specifically, the
transfer device 300 has twomedicine containers 340. One of themedicine containers 340 is provided at one side in a widthwise direction of thecover 331 relative to the turningshaft 318, while the other medicine container is provided at the other side in a widthwise direction of thecover 331 relative to the turning shaft. Side surfaces 340 a, 340 b of themedicine container 340 are locatedopposite guide rails guide rails Roller attaching members roller attaching member 343 has: a fixingportion 343 a fixed to theside surface 340 a; avertical portion 343 b opposite thereto; and ahorizontal portion 343 c disposed between the fixingportion 343 a and thevertical portion 343 b and approximately parallel to thebase plate 311. - A
guide roller 346 is rotatably provided on thevertical portion 343 b. Theguide roller 346 is fitted to theguide rail 332 arranged along the turningshaft 318. Further, the sandwichingmember 344 is mounted on thevertical portion 343 b and thetiming belt 337 is fitted between the sandwichingmember 344 and thevertical portion 343 b. This allows themedicine container 340 to be connected to the timing belt 338. - In this case, the
transfer device 300 includes twomedicine containers medicine container 340 of said two medicine containers (aleft medicine container 340 in an example illustrated inFIGS. 32 and 33 ) (hereinafter, this may be referred to as a drive side medicine container 340) has aguide roller 347 on thehorizontal part 343 c. Theguide roller 347 is rotatably provided at a shaft approximately vertically fixed to thehorizontal portion 343 c and protruding downward therefrom. Theguide roller 347 is fitted to thegroove 325 formed between theguide rails base plate 311. - Meanwhile, a
roller attaching member 345 is attached to theside surface 340 b of themedicine container 340. Theroller attaching member 345 has: a fixingportion 345 a fixed to theside surface 340 b; avertical portion 345 b opposed thereto; and ahorizontal portion 345 c connecting the fixingportion 345 a and thevertical portion 345 b. Thevertical portion 345 b is also opposite theguide rail 333 attached to thelong side cover 331. Aguide roller 348 is rotatably attached to thevertical portion 345 b and is fitted to theguide rail 333. - The
transfer device 300 is configured as described above and is positioned as inserted to thecommunication opening 4 b of thewall surface 4 a between themain unit 2 and thesub unit 3. Specifically, thetransfer device 300 is horizontally disposed with thebase part 310 facing downward and theturn part 330 facing upward. Further, thetransfer device 300 is disposed such that the receivingopening 331 d provided in thecover 331 is located at thesub unit 3 and thedispensing opening 320 provided in thebase plate 311 is located at themain unit 2. - Next, operation of the
transfer device 300 will be described. Thetransfer device 300 can turn theturn part 330 about the turningshaft 318 while moving twomedicine containers 340 provided in theturn part 330 along theguide rails drive motor 313 provided in thebase part 310. More specifically, if thedrive motor 313 operates, theturn drive gear 316 coupled to the rotating shaft of thedrive motor 313 and the turn drivengear 317 meshed with theturn drive gear 316 rotate. Thus, the turningshaft 318 with the turn drivengear 317 rotates and thus theentire turn part 330 rotate about the turningshaft 318. - In this case, as described above, the
guide roller 347, which is rotatable about the shaft protruding downward, is provided in one of the twomedicine containers 340, 340 (the drive side medicine container 340). Theguide roller 347 is fitted to thegroove 325 formed between theguide rails base part 310. Further, as shown inFIG. 32 , thegroove 325 is curved convexly toward one side in the width direction like theguide rails side medicine container 340 are restricted by thegroove 325. Further, other component members for constituting theturn part 330 are assembled to thecover 331 like the driveside medicine container 340 and those are integrally rotatble about the turningshaft 318. Thus, when theturn part 330 rotates clockwise by the operation of thedrive motor 313 in a state shown inFIG. 32 , theentire turn part 330 is turned about the turningshaft 318 while guided by thegroove 325 and theguide roller 347 and the driveside medicine container 340 advance toward the one end of the groove 325 (upward inFIG. 32 ). Also, as shown inFIG. 34 , when theturn part 330 is turned at a predetermined angle about the turningshaft 318, the driveside medicine container 340 reach the vicinity of the timingpulley 336 disposed at the one end of the groove 325 (upper side inFIG. 34 ). - Further, as described above, the drive
side medicine container 340 and theother medicine container 340 without the guide roller 347 (hereinafter, this may be referred to as a driven side medicine container 340) are fixed to thetiming belt 337 respectively by the sandwichingmember 344 attached to thevertical portion 343 b of theroller attaching member 343. Thus, when the driveside medicine container 340 advance toward one end of thegroove 325 along with the turning of theturn part 330, the drivenside medicine container 340 advances toward the other end of thegroove 325, that is, toward the timingpulley 335. - Then, when the driven
side medicine container 340 reaches the dispensingopening 320 provided in thebase plate 311 as shown inFIG. 34 , thecontact portion 342 a of theshutter 342 disposed at the bottom surface of the drivenside medicine container 340 is brought into contact with thecontact member 321 attached to the surface of thebase plate 311. Thus, theshutter 342 is pushed and opened and thus the medicines therein are dispensed downward, that is, toward thesub collecting hopper 87 in themain unit 2. Meanwhile, in the state shown inFIG. 34 , the driveside medicine container 340 reaches a position corresponding to the receivingopening 331 d provided in thetop surface 331 a of thecover 331. Thus, in the state shown inFIG. 34 , the medicine dispensed in thesub unit 3 can be inputted to the drive side medicine container through thesub hopper 135. - Meanwhile, in the states shown in
FIGS. 32 and 34 , if thedrive motor 313 provided in thebase part 310 operates so as to rotate the rotating shaft in a direction opposite to the above, theturn part 330 rotates counterclockwise about the turning shaft 318 (when viewed downwardly). Accordingly, the driveside medicine container 340 and theguide roller 347 attached thereto advance toward the dispensing opening 320 (downward in the state shown inFIGS. 32 and 34 ) while guided by thegroove 325. Then, as shown inFIG. 35 , if theturn part 330 rotates counterclockwise about the turningshaft 318 at a predetermined angle, the driveside medicine container 340 reaches a position corresponding to thedispensing opening 320. Thus, theshutter 342 disposed at an inside portion of the driveside medicine container 340 is opened and the medicines inputted thereto are dispensed to thesub collecting hopper 87 in themain unit 2 disposed below the shutter. Meanwhile, the drivenside medicine container 340 reaches the position corresponding to the receivingopening 331 d concomitantly with the operation of the driveside medicine container 340. Thus, the medicines dispensed in thesub unit 3 can be inputted to the drivenside medicine container 340. - The above-described
transfer device 300 is configured to transfer the medicines between themain unit 2 and thesub unit 3 by turning theentire turn part 330 about the turningshaft 318 and by reciprocating each of themedicine containers turn part 330 by means of power produced by the turning movement. Thus, when employing thetransfer device 300, it is possible to provide amedicine dispensing system 1 that can transfer the medicines dispensed in thesub unit 3 to themain unit 3 to pack and dispense the same together with the medicines dispensed in themain unit 3, similarly to the case of employing thetransfer device - The
transfer device 300 obtains power for the turning movement of theturn part 330 and the reciprocating movement of themedicine containers 340 from thedrive motor 313 provided in thebase part 310. However, the present invention should not be limited to such configuration. For example, a power source for turning theturn part 330 and a power source for reciprocating themedicine containers 340 may be separately provided. - More specifically, the
transfer device 300 may be configured such that theguide roller 347 provided in the driveside medicine container 340 and theguide rail 323 attached to thebase plate 311 are omitted and at least one of the timing pulleys 335, 336 is rotated by a power source different from that of thedrive motor 313. According to such configuration, theturn part 330 is turned by thedrive motor 313, and thetiming belt 337 wound between the timing pulleys 335, 336 is operated by the separately-provided power source, thereby reciprocating themedicine containers 340 between the dispensingopening 320 and receivingopening 331 d. - The
medicine dispensing system 1 is not limited to employing the above-describedtransfer device transfer device 400 shown inFIG. 36 . Thetransfer device 400 is configured similar to the above-describedtransfer device 5 in that the medicine dispensed in thesub unit 3 are transferred to themain unit 2 by means of an airflow. However, a device configuration and medicine transferring processes of thetransfer device 400 are different from those of thetransfer device 5. Specifically, thetransfer device 400 has amedicine receiving part 401 for receiving the medicine dispensed in thesub unit 3, and amedicine dispensing part 402 for receiving and dispensing the medicines transferred from thesub unit 3. Themedicine receiving part 401 and themedicine dispensing part 402 are a hollow member having a shape of a measure capable of storing medicines. Further, thetransfer device 400 has aforward pipe line 403 configured to connect themedicine receiving part 401 and themedicine dispensing part 402. - The
blower 405 is connected to themedicine receiving part 401 through apipe 406. Further, ablower shutter 407 is provided at a connection portion between themedicine receiving part 401 and thepipe 406. Thus, when theblower 406 operates and theblower shutter 407 is opened, an airflow can be produced through thepipe 406 to themedicine receiving part 401. - A
pump 408 is connected to themedicine dispensing part 402 through anexhaust pipe line 410. Thetransfer device 400 can introduce air into themedicine receiving part 401 through thepipe 406 and produce airflow flowing through theforward pipe line 403 from themedicine storing part 40 toward themedicine dispensing part 402 by operation ofblower 405. Further, thetransfer device 400 can produce airflow flowing through theexhaust pipe line 410 from inside themedicine dispensing part 402 toward an outside portion thereof. - As shown in
FIG. 37 , themedicine dispensing part 402 is configured to be surrounded by peripheral surfaces and to be closed at a top surface. Themedicine dispensing part 402 has an introducingopening 412 and anexhaust opening 413 at one of the peripheral surfaces of the medicine dispensing part 402 (hereinafter, this may be referred to as a peripheral surface 411) and adispensing opening 415 at itsbottom surface 414. The introducingopening 412 and theexhausting opening 413 are vertically juxtaposed. Theforward pipe line 403 is connected to the introducingopening 412, while theexhaust pipe line 410 is connected to theexhaust opening 413. As shown inFIG. 38 , theforward pipe line 403 has a stayingportion 416 at its end portion, to which the introducingopening 412 is connected. The stayingportion 416 is formed such that a peripheral surface of theforward pipe line 403 becomes thinner in thickness toward a forward end. Theforward pipe line 403 is inserted and connected to the introducingopening 412 with the stayingportion 416 facing downward. Thus, the medicines transferred through theforward pipe line 403 can stay in the stayingportion 416. - Further, the
forward pipe line 403 hasair orifices 417 near themedicine dispensing part 402 and apart from an inserting portion to the introducingopening 412. The air orifices 417 are orifices for exhausting the airflow flowing within theforward pipe line 403. The air orifices 417 are much smaller than the medicines and are exposed outside themedicine dispensing part 402. Thus, even if the end portion of theforward pipe line 403 with the stayingportion 416 becomes closed, the airflow flowing from themedicine receiving part 401 toward themedicine dispensing part 402 in theforward pipe line 403 can be produced through the operation of theblower 405. - As shown in
FIGS. 37 and 38 , themedicine dispensing part 402 is provided with ashutter 420. As shown inFIG. 39 , theshutter 420 includes a metallic plate having an L-shaped cross-section and an inclined plate integrally formed therewith. Theshutter 420 is configured to open and close the introducingopening 412 and theexhaust opening 413 is provided in theperipheral surface 411 as well as the dispensingopening 415 formed on abottom surface 414. More specifically, theshutter 420 includes: afirst shutter surface 421; asecond shutter surface 422 perpendicular to thefirst shutter surface 421; and an inclined surface 423 (i.e., a partitioning means) inclined relative to the first and second shutter surfaces 421, 422. Further, thesecond shutter surface 422 is provided with a protrudingportion 425 which slightly protrudes beyond an intersection between thefirst shutter surface 421 and thesecond shutter surface 422. - The
shutter 420 is positioned in such a manner that an upper end of thefirst shutter surface 421 is fitted to agroove 426 formed on a top surface of themedicine dispensing part 402 and theprotrusion 425, and anedge portion 427 of thesecond shutter surface 422 are fitted to guidepulleys bottom surface 414 of themedicine dispensing part 402. Further, theshutter 420 is inserted toslits peripheral surfaces peripheral surface 414 of themedicine dispensing part 402. Theshutter 420 is configured such that the first and second shutter surfaces 421, 422 can freely slide along theperipheral surface 411 and thebottom surface 414 of themedicine dispensing part 402 and theinclined surface 423 can freely slide as obliquely traversing an internal space of themedicine dispensing part 402 by a power from a power source (not shown). - In the
shutter 420, a length in the above-described slide direction (a length in a lengthwise direction) is set to be about twice the width of the medicine dispensing part 402 (a widthwise length of the peripheral surface 411). The first and second shutter surfaces 421, 422 and theinclined surface 423 are configured differently in one area (in this case, this may be referred to as an area A) and the other area (in this case, this may be referred to as an area B) relative to half a length in a lengthwise direction. Specifically, the area A of thefirst shutter surface 421 is provided with twoopenings openings openings opening 412 and theexhaust opening 413 formed on theperipheral surface 411 of themedicine dispensing part 402 respectively. Further, an air-permeable filter 440 is provided in a position corresponding to theopening 436. Meanwhile, the area B of the first shutter surface 421 (e.g., a forward isolation portion 442), which is a portion for blocking theforward pipe line 403, is provided with abuffer material 441. Thebutter material 441 buffers an impact exerted on the medicine due to a collision of the medicine flowing in through theforward pipe line 403 while the introducingopening 412 is blocked by thefirst shutter surface 421. Thebuffer material 441 may include a rubber, a sponge, a foamed styrofoam, etc. - As shown in
FIG. 40( b), the area B of thesecond shutter surface 422 is provided with anopening 437 which communicates with the dispensingopening 415 provided on thebottom surface 414 of themedicine dispensing part 402, while the area A is not provided with any opening. As shown inFIG. 40( a), the area B of theinclined surface 423 is provided with an opening 438, while the area A is not provided with any opening. - The
shutter 420 is configured as described above. Thus, when the area A of theshutter 420 is positioned within themedicine dispensing part 402 and the area B is outwardly exposed as shown inFIG. 37( a), the internal space of themedicine dispensing part 402 is partitioned into two sections by theinclined surface 423 as shown inFIG. 38 . Therefore, theforward pipe line 403 and theexhaust pipe line 410 communicate with each other through the introducingopening 412 and theexhaust opening 413 in the space above theinclined surface 423. Further, the dispensingopening 415 is blocked by thesecond shutter surface 422. Thus, the medicine transferred from themain unit 2 through theforward pipe line 403 is allowed to be received within the space above theinclined surface 423 in themedicine dispensing part 402. - When the area B of the
shutter 420 is positioned within themedicine dispensing part 402 as shown inFIG. 37( b), the introducingopening 412 and theexhaust opening 413 are blocked by thefirst shutter surface 421. Meanwhile, the medicine stored within themedicine dispensing part 402 is capable of being dispensed from the dispensingopening 415 through theopenings 437, 438 provided on thesecond shutter surface 422 and theinclined surface 423. - Next, operation of the
transfer device 400 will be described. Thetransfer device 400 can transfer the medicine from thesub unit 3 to themain unit 2 by sequentially repeating a medicine transferring operation for transferring the medicine dispensed to themedicine receiving part 401 in thesub unit 3 to the vicinity of themedicine dispensing part 402 and a medicine introducing operation for introducing the medicine transferred by the medicine transferring operation into themedicine dispensing part 402. - When performing the medicine transferring operation, in the
transfer device 400, a position of theshutter 420 is adjusted such that the area B is positioned in the position of themedicine dispensing part 402 as shown inFIG. 37( b). Therefore, a distal end of theforward pipe line 403 is blocked by thefirst shutter surface 421 of theshutter 420. When performing the medicine transferring operation, theblower 405 operates in such a state. Thus, an airflow flowing from themedicine receiving part 401 toward themedicine dispensing part 402 is produced within theforward pipe line 403. In this case, the airflow flowing within theforward pipe line 403 is enough to transfer the medicine. A flow rate and a flow velocity of the airflow are not so great. If the airflow is produced within theforward pipe line 403 as described above, the medicine, which is dispensed to themedicine receiving part 401 of thesub unit 3, flows to themain unit 2 to thereby be retained in the stayingportion 416 provided in the vicinity of the introducingopening 412 of themedicine dispensing part 402. Thus, the medicine transferring operation is completed. - If the medicine transferring operation is completed as described above, the
transfer device 400 proceeds with the medicine introducing operation. When performing the medicine introducing operation, as shown inFIG. 37( a), the position of theshutter 420 is adjusted such that the area A of theshutter 420 reaches a position corresponding to themedicine dispensing part 402. Thus, the introducingopening 412 and theexhausting opening 413 of themedicine dispensing part 402, which has been blocked by thefirst shutter surface 421, are opened, while the dispensingopening 415 is closed by thesecond shutter surface 422. Further, the internal space of themedicine dispensing part 402 is partitioned by theinclined surface 423. In this state, thepump 408 connected to theexhaust pipe line 410 operates and therefore the air within themedicine dispensing part 402 is sucked and exhausted. As a result, the medicine, which has been transferred to the stayingportion 416 in the vicinity of the introducingopening 412 through the previously-performed medicine transferring operation, is introduced into themedicine dispensing part 402. The medicine introduced into themedicine dispensing part 402 is inhibited from flowing into theexhaust pipe line 410 by thefilter 440 provided on thefirst shutter surface 421 of theshutter 420 and therefore stays within themedicine dispensing part 402. If the medicine transferred through theforward pipe line 403 is introduced into themedicine dispensing part 402 as described above, the medicine introducing operation is completed. - As described above, the
transfer device 400 first transfers the medicine from themedicine dispensing part 402 to themedicine receiving part 401 through the medicine transferring operation and then can introduce the medicine transferred as such into themedicine receiving part 401 through the medicine introducing operation. Accordingly, in case of employing thetransfer device 400, it is possible to deliver the medicine from themedicine dispensing part 402 tomedicine receiving part 401 by repeating the medicine transferring operation and the medicine introducing operation, similar to the case of employing saidtransfer device - Further, in the case of employing the
transfer device 400, the medicine transferring operation and the medicine introducing operation are performed independently. Accordingly, the flow velocity of the airflow, which flows within theforward pipe line 403 by the operation of theblower 405 during the medicine transferring operation, is sufficient to transfer the medicine. It does not need to increase excessively. More specifically, the flow velocity of the airflow, which flows within theforward pipe line 403 by operation of theblower 405 in the medicine transferring operation, is equal to or lower than the flow velocity of the airflow flowing by the operation of thepump 408 during the medicine introducing operation. Accordingly, in the case of employing thetransfer device 400, it is possible to prevent the medicine from breaking or chipping due to the collision between the medicines which are transferred from themain unit 2 to thesub unit 3 or between the medicines and theshutter 420. - Further, in the above-described
transfer device 400, although the medicine transferred in the medicine transferring operation collides against theshutter 420, an impact on the medicine is buffered by thebuffer material 441 provided on theshutter 420. Thus, according to the above-described configuration, it is possible to prevent the medicine from breaking or chipping due to the collision against theshutter 420 in the medicine transferring operation. Further, it is illustrated in the present embodiment that thebuffer material 441 prevents the medicine from breaking or chipping. However, the present invention should not be limited to such a configuration. Thebuffer material 441 may not be employed. - As described above, the
transfer device 400 has inclinedsurface 423 at theshutter 420 and can partition the internal space of themedicine dispensing part 402 by theinclined surface 423. Further, theinclined surface 423 is integrally formed in theshutter 420 and partitions the internal space of themedicine dispensing part 402 along with the open state of the introducingopening 412 or theexhaust opening 413. Therefore, a size of a space in which theexhaust pipe line 410 and theforward pipe line 403 communicates with each other (e.g., a space above the inclined surface 423) can be sufficiently smaller than a size of the internal space of themedicine dispensing part 402. Accordingly, thetransfer device 400 can introduce the medicine transferred through theforward pipe line 403 into themedicine dispensing part 402 without significantly increasing an output (an exhaust capacity) of thepump 408 during the medicine introducing operation. Further, since there is no need to significantly increase the output of thepump 408 during the medicine introducing operation, the medicine is not subjected to great impact when introduced into themedicine dispensing part 402. As a result, it is possible to more surely prevent the medicine from breaking or chipping. - It is illustrated that the
transfer device 400 has inclinedsurface 423 integrally mounted to theshutter 420. However, the present invention should not be limited to such a configuration. Theinclined surface 423 may be configured to operate independently of theshutter 420. Further, thetransfer device 400 has theinclined surface 423. However, the transfer device may not include theinclined surface 423. - As described above, the
inclined surface 423 is disposed opposite the introducingopening 412 and theexhausting opening 413. Further, in themedicine dispensing part 402, a distance between theinclined surface 423 and theexhaust opening 413 positioned at downstream of the airflow flowing during transferring or introducing the medicine is narrower than a distance between theinclined surface 423 and the introducingopening 412 positioned upstream of the airflow. Thus, if theinclined surface 423 is disposed as described above, the air introduced from the introducingopening 413 into themedicine dispensing part 402 impinges against theinclined surface 423 and then changes its direction to flow smoothly toward theexhaust opening 413. - Further, the above-described
transfer device 400 is configured to head the air exhausted from theexhaust pipe line 410 outside. However, the present invention should not be limited to such a configuration. Specifically, as shown inFIG. 41 , theexhaust pipe line 410 may be connected to themedicine receiving part 401 and themedicine dispensing part 402 in the same manner as theforward pipe line 403. According to such a configuration, a circulation system, which circulates the air between themedicine receiving part 401 and themedicine dispensing part 402, is formed. - Further, as shown in
FIG. 41 , when theexhaust pipe line 410 is connected to themedicine receiving part 401 to form the circulation system, the air circulates within the closed space generating heat. Therefore, in case of dealing with medicines which can be denatured by heat and connecting theexhaust pipe line 410 to themedicine receiving part 401, it is preferred that a cooling means for cooling the air may be disposed at a suitable place such as at a halfway point of theexhaust pipe line 410, and that the circulation system may be configured to appropriately introduce external air with low temperature. - The above-described
transfer device 400 has a flow path, which runs from themedicine receiving part 401 through theforward pipe line 403 and themedicine dispensing part 402 to theexhaust pipe line 410 and produces airflow within the flow path along with the transfer of the medicine between themedicine receiving part 401 andmedicine dispensing part 402. Further, similar to the case where theexhaust pipe line 410 is connected to themedicine receiving part 401 as shown inFIG. 41 , the airflow is produced within the circulating flow path connecting themedicine receiving part 401 andmedicine dispensing part 402 with theforward pipe line 403 and theexhaust pipe line 410. Since the above-describedtransfer device 400 includes thefilter 440 provided on themedicine dispensing part 402 constituting a part of the flow path, it is preferred that the transfer device is configured to exactly detect a block of thefilter 440 and to perform maintenance therefor. Thus, thetransfer device 400 may include a flow-amount detecting means for detecting the amount of air flowing within the flow path and a clogging judging means. When the flow-amount detected by the flow-amount detecting means is less than a predetermined amount, the clogging judging means may decide that thefilter 440 is clogged. - Further, in case of providing the flow-amount detecting means to judge the clogging of the
filter 440 as described above, the medicine under transfer to themedicine dispensing part 402 provided in themain unit 2 may be transferred by increasing the output of one or both of theblower 405 and thepump 408 when the clogging occurs and then to stop transferring the medicine or notify the clogging of thefilter 440. More specifically, the medicine under transfer may be completely transferred by increasing the output of one or both of theblower 405 and thepump 408 upon a condition that the flow-amount detected by the flow-amount detecting means decreases. Thereafter, based on the above-mentioned increases in the output of theblower 405 or thepump 408, the clogging of thefilter 440 may be decided by the clogging judging means or transferring the next medicine may not be performed. - It is illustrated in the above-described embodiment that the
filter 440 is provided in the flow path along which the airflow flows during the transfer of the medicine. However, the present invention should not be limited to such a configuration. A separate filter may be provided at any other place or thefilter 440 may not be provided. - The
medicine dispensing system 1 is not limited to employing thetransfer device transfer device 500 shown inFIG. 42 . Thetransfer device 500 includes: aforward pipe line 502; a blower 504 (an airflow producing means); a medicine dispensing part 510 (a delivering part); and amedicine receiving part 511. Thetransfer device 500 is configured similarly to the above-describedtransfer device 400 in that medicines are transferred by the airflow produced within theforward pipe line 502 by an operation of theblower 504. However, thetransfer device 500 is configured differently from the above-describedtransfer device 400 in that it does not need thepump 408 or a pipe such as theexhaust pipe line 410 for exhausting the airflow introduced into themedicine dispensing part 510. - More specifically, the
forward pipe line 502 of thetransfer device 500 includes a pipe which connects amain storage part 20 and asub storage part 120. Theblower 504 is disposed so as to produce airflow from thesub unit 3 toward themain unit 2 within theforward pipe line 502. - As shown in
FIGS. 44 to 47 , themedicine dispensing part 510 is configured such that adelivery container 512 connected to theforward pipe line 502 is housed in a box-shapedouter container 530. Thedelivery container 512 is a hollow box-shaped member that is surrounded byside surfaces 512 a to 512 d. The delivery container includes ashutter 514 and a buffer means 522. Thedelivery container 512 includes anupper container body 524 and alower container body 526, which are vertically combined. An inside portion of thedelivery container 512 can be swept by removing theupper container body 524 of an upper side from thelower container body 526, if necessary. - As shown in
FIGS. 46 and 47 , theupper container body 524 is a hollow member constituting an upper portion of thedelivery container 512. Further, theupper container body 524 is opened at a bottom portion coupled to thelower container body 526. When thedelivery container 512 is assembled, theforward pipe line 502 is connected to a surface constituting theside surface 512 a of theupper container body 524 via ajoint pipe 540. Thejoint pipe 540 includes a pipe more flexible than theforward pipe line 502, such as a rubber pipe. - Further, a buffer means 522 is provided at the
upper container body 524. The buffer means 522 includes a plate member, on which an elastic material such as rubber is provided or coated, or a rubber plate elastic in itself. The buffer means 522 is disposed opposite thesurface 512 a connected to theforward pipe line 502 within theupper container body 524. Specifically, the buffer means 522 is obliquely downwardly disposed across theside surface 512 d and thetop surface 512 e. - In the
upper container body 524, a surface, which crosses the surface (theside surface 512 a) connected to the forward pipe line 502 (in the present embodiment, approximately crossing at a right angle) and constitutes the side surfaces 512 b, 512 c when thedelivery container 512 is assembled, is formed with a plurality ofexhausting holes 524 p. In this case, the side surfaces 512 b, 512 c are surfaces laterally disposed relative to the airflow introduced into thedelivery container 512 through theforward pipe line 502. Further, theexhausting holes 524 p are disposed below a height of connection to theforward pipe line 502. More specifically, theexhausting holes 524 p are disposed below a central axis LU centrally extending through an opening area of theforward pipe line 502. Thus, the airflow introduced through theforward pipe line 502 flows downward without being stagnant or forming a vortex within the upper section of thedelivery container 512. Also, the airflow is directed so as to flow in a direction crossing direction the airflow is introduced into thedelivery container 512. - As shown in
FIGS. 46 and 47 , thelower container body 526 is a hollow member constituting a lower portion of thedelivery container 512. Abottom portion 518 of thelower container body 526 is formed with adispensing opening 520 for dispensing the medicine toward themedicine preparing part 80. Further, thelower container body 526 is open at a top portion coupled to theupper container body 524. Accordingly, thelower container body 526 is integrally coupled to theupper container body 524 to thereby form a hollowinternal space 516 within the upper andlower container bodies - In the
lower container body 526, a surface, which constitutes the side surfaces 512 b, 512 c when thedelivery container 512 is assembled, is formed with a plurality ofexhausting holes 526 p. That is, theexhausting holes 526 p are formed in surfaces (the side surfaces 512 b, 512 c) laterally disposed relative to the airflow introduced into thedelivery container 512 through theforward pipe line 502. Further, theexhausting holes 526 p are positioned at a lower side of thelower container body 526. More specifically, theexhausting holes 526 p are positioned below a reference plane LD passing through a position where a supportingshaft 552 of theshutter 514 is provided. Thus, in the airflow introduced into theupper container body 524 through theforward pipe line 502, the airflow, which flows downward to come to thelower container body 526, flows further downward within thelower container body 526. Also, the airflow is directed so as to flow in the direction crossing the introducing direction into thedelivery container 512. Accordingly, the medicine, which has dropped to thelower container body 526, surely falls on theshutter 514. - As shown in
FIGS. 46 and 47 , theshutter 514 serves to open and close the dispensingopening 520 provided at thebottom portions 518 and is positioned in thelower container body 526 of thedelivery container 512. Theshutter 514 includes a plate body having a cross section of a flat rhombus shape with pointed tips. A thickness of the plate body becomes gradually thinner as toward opposite ends of the plate body. - The
shutter 514 is disposed rotatably about the supportingshaft 552 within thedelivery container 512. The supportingshaft 552 is approximately perpendicular to the side surfaces 512 b, 512 c constituting thedelivery container 512. The supporting shaft is connected to adrive device 550 provided outside of theouter container 530 of themedicine dispensing part 510. Thedrive device 550 includes amotor 550 a and apower transmission mechanism 550 b. A rotating power produced by themotor 550 a is transmitted to theshutter 514 via the supportingshaft 552 to thereby change an orientation of theshutter 514. - The
shutter 514 can vertically partition theinternal space 516 of thedelivery container 512 by placing its tip edges into contact with the side surfaces 512 a, 512 d of thedelivery container 512. If theinternal space 516 is vertically partitioned by theshutter 514, then thedelivery container 512 goes into a state where the medicine is not allowed to be dispensed from the dispensing opening 520 (hereinafter, this state may be referred to as a closed state). Further, theinternal space 516 of thedelivery container 512 can vertically communicate by rotating theshutter 514 about the supportingshaft 552. If an inclination of the shutter becomes steeper than that in the closed state and theinternal space 516 in which it vertically communicates, then thedelivery container 512 goes into a state where the medicine is allowed to be dispensed from the dispensing opening 520 (hereinafter, this state may be referred to as an open sate). Therefore, as the inclination of theshutter 514 is changed by the operation of thedrive device 550, thedelivery container 512 can change between a closed state and the open state. - The
delivery container 512 is housed in a space enclosed by theouter container 530. Theouter container 530 is a hollow box-shaped body surrounded by fourperipheral surfaces 530 a to 530 d. It is possible to sweep or maintain thedelivery container 512 since alid 530 f provided on atop surface 530 e of theouter container 530 is appropriately opened and closed. - The
peripheral surface 530 a constituting theouter container 530 is penetrated by theforward pipe line 502 connected to thedelivery container 512 housed in theouter container 530. Further, each of theperipheral surfaces peripheral surface 530 a (in the present embodiment, approximately crossing at a right angle), while theperipheral surface 530 d is opposite theperipheral surface 530 a. As shown inFIGS. 44 , 45 and 47, the above-describeddelivery container 512 is positioned near a corner formed by theperipheral surfaces outer container 530. That is, theperipheral surfaces delivery container 512, respectively, while distances between theperipheral surfaces peripheral surface 530 a and theside surface 512 a is much larger than the distance between theperipheral surface 530 d and theside surface 512 d. Also, theperipheral surface 530 d and theside surface 512 d are positioned almost without a gap therebetween. Further, the distance between theperipheral surface 530 b and theside surface 512 b is smaller than the distance between theperipheral surface 530 c and theside surface 512 c. - The
outer container 530 has anexhausting part 532 for exhausting the air flowing out from theexhausting holes delivery container 512 at theperipheral surface 530 c. Theexhausting part 532 is positioned near theperipheral surface 530 a of theouter container 530. Theexhausting part 532 is provided with aprimary filter 534 and asecondary filter 536 with meshes finer than those of theprimary filter 534. Theprimary filter 534 and thesecondary filter 536 can be detached separately for purposes of cleaning or replacement. Theprimary filter 534 with sparse meshes is disposed upstream in a flow direction of the air exhausted from theexhausting part 532 relative to thesecondary filter 536 with fine meshes. In the present embodiment, theprimary filter 534 is disposed in theexhausting part 532 inward of theouter container 530, while thesecondary filter 536 is disposed outward of theouter container 530. - Meanwhile, as shown in
FIG. 42 , themedicine receiving part 511 provided in thesub unit 3 is comprised of a box-shaped body with an opened medicine input opening 560 at its top surface. Thesub hopper 135 provided in thesub unit 3 is connected to themedicine input opening 560. The medicine dispensed from thesub storage part 120 is inputted into themedicine receiving part 511 through themedicine input opening 560. As shown inFIGS. 42 and 48 , both the one end of theforward pipe line 502 and ablower pipe 566 connected to theblower 504 are connected to themedicine receiving part 511 to communicate with each other. Amedicine transfer passage 562 and amedicine input passage 564 extending from the medicine input opening 560 to theforward pipe line 502 are provided within themedicine receiving part 511. - The
forward pipe line 502 and theblower pipe 566 are connected to themedicine transfer passage 562. As indicated by an arrow inFIG. 48 , as theblower 504 operates, airflow is produced toward theforward pipe line 502. Themedicine transfer passage 562 joins themedicine input passage 564 at its halfway portion. Themedicine transfer passage 562 has anenlarged diameter section 568, at which a cross section of the flow passage is enlarged, downstream of ajunction 566 with the medicine input passage 564 (i.e., at a portion connected to the forward pipe line 502). A diameter of theenlarged diameter section 568 is enlarged toward the medicine input passage 564 (i.e., toward an upper side) within themedicine receiving part 511. In the present embodiment, themedicine transfer passage 562 is configured such that an inner diameter of theenlarged diameter section 568 is enlarged to be about 1.5 times larger than that of anupstream portion 567. Meanwhile, themedicine transfer passage 562 is configured such that a portion upstream of the junction 566 (hereinafter, this may be referred to as theupstream portion 567″) and theenlarged diameter section 568 are flush with each other at a portion opposite the medicine input passage 564 (i.e., a bottom side of the medicine receiving part 511). Thus, the airflow flowing within themedicine transfer passage 564 smoothly flows toward theforward pipe line 502 without being stagnant or forming a vortex at thejunction 566. - Further, the
medicine input passage 564 is gently inclined downward from themedicine input opening 560 and is joined to themedicine transfer passage 562. Thus, if the airflow is produced by operation of theblower 504 within themedicine transfer passage 562, then a suction force from the medicine input opening 560 toward themedicine transfer passage 562 is produced at themedicine input passage 564. Accordingly, if the medicine is inputted into themedicine input opening 560, as indicated by a two dot chain line inFIG. 48 , the medicine is sucked and introduced into themedicine transfer passage 562 and then is introduced to theforward pipe line 502. - Next, operation of the
transfer device 500 will be described. Thetransfer device 500 starts transferring the medicine by dispensing the medicine from thesub storage part 120 of thesub unit 3. If the medicine dispensed from thesub storage part 120 is introduced into theforward pipe line 502 through themedicine receiving part 511, then theblower 504 operates to produce the airflow from thesub unit 3 toward themain unit 2 within theforward pipe line 502. Thus, the medicine flows to themedicine dispensing part 510 provided in themain unit 2. In this case, as shown inFIG. 46 , theshutter 514 provided in thedelivery container 512 in themedicine dispensing part 510 of themain unit 2 goes into the closed state. - When the medicine dispensed in the
sub unit 3 reaches themedicine dispensing part 510, it is introduced into thedelivery container 512. In this case, if the airflow is strong over the weight or quantity of the medicine, the medicine collides against the buffer means 522 and then drops downward in theinternal space 516 of thedelivery container 512. However, if the airflow is not so strong, the medicine drops downward in theinternal space 516 without collision against the buffer means 522. Further, after the airflow introduced into thedelivery container 512 through theforward pipe line 502 flows downward in theinternal space 516, as indicated by an arrow inFIG. 47 , it is exhausted from theexhausting holes delivery container 512 drops smoothly. The medicine dropping within thedelivery container 512 falls on theshutter 514 in the closed state. - If all the medicines transferred from the
sub unit 3 falls on theshutter 514 as described above, theshutter 514 is changed into the open state. In such a case, the medicine falls along the surface of theshutter 514 which becomes gradually steeper and then is dispensed from the dispensingopening 520 provided on thebottom portion 518 of thedelivery container 512. The medicine dispensed from the dispensingopening 520 is inputted into themedicine preparing part 80 provided below themedicine dispensing part 510 for packing in themedicine packing part 21 provided in themain unit 2. Thereafter, the medicines prepared in themedicine preparing part 80 are packed by themedicine packing part 21 one after another. - In case of employing the
transfer device 500, it is possible to transfer the medicine from thesub unit 3 tomain unit 2 to pack the same as described above, but also to sweep the inside of the medicine transfer path of thetransfer device 500 by means of airflow produced by theblower 504. Specifically, when sweeping the inside of the medicine transfer path of thetransfer device 500, theblower 504 operates as theshutter 514 is closed. In this case, the output of theblower 504 is set to be larger than the transfer of the medicine. Thus, dusts remaining within the medicine transfer path of thetransfer device 500 are swept off and then expelled from theexhausting holes delivery container 512. The dusts expelled from theexhausting holes primary filter 534 and thesecondary filter 536 provided in theexhausting part 532 of theouter container 530. - As described above, the
medicine dispensing system 1 employing thetransfer device 500 can transfer the medicine from thesub unit 3 to themedicine dispensing part 510 provided in themain unit 2 along with the airflow produced by the operation of theblower 504. Further, after the medicine is transferred to themedicine dispensing part 510, the medicine can be dispensed for packing by changing theshutter 514 to the open state. Accordingly, in case of employing thetransfer device 500, similarly to the case employing the above-describedtransfer device sub unit 3 at themedicine packing part 21 provided in themain unit 2. - In the above-described
transfer device 500, theexhausting holes delivery container 512 and theforward pipe line 502. Thus, the airflow introduced into thedelivery container 512 through theforward pipe line 502 flows downward. Further, in the above-describeddelivery container 512, the side surfaces 512 b, 512 c, which are disposed laterally to theside surface 512 a connected to theforward pipe line 502, are provided approximately symmetrically. Thus, the airflow introduced into thedelivery container 512 flows downward as described above and then is smoothly exhausted as bifurcated. As such, in thetransfer device 500, the airflow introduced into thedelivery container 512 smoothly flows downward and is exhausted without being stagnant at the upper side. Thus, the medicine introduced on the airflow drops smoothly without blowing within thedelivery container 512 and is to be dispensed. - As described above, since the airflow smoothly flows and the medicine smoothly drops within the
delivery container 512, thetransfer device 500 does not need thepump 408 or theexhaust pipe line 410 for exhaust purposes as described in thetransfer device 400. Accordingly, in case of employing thetransfer device 500, a device configuration can be simplified when compared to the case of employing thetransfer device 400. - It is illustrated in the present embodiment that the
exhausting holes delivery container 512. However, an equivalent to theexhausting holes exhausting holes exhausting holes - Further, it is illustrated in the present embodiment that the
exhausting holes upper container body 524 and thelower container body 526. However, the present invention should not be limited to such a configuration. One of theexhausting holes openings delivery container 512, the airflow, in some embodiments, is exhausted not in a halfway position in a height direction of thedelivery container 512, but in a position as low as possible. Accordingly, in case of forming any one of theexhausting holes 524 p and theexhausting holes 526 p, it is preferred to form only theexhausting holes 526 p. Further, in case of varying the number or the opening area of theexhausting holes exhausting holes 524 p, in some embodiments, is smaller than those of theexhausting holes 526 p. - In the above-described
transfer device 500, the buffer means 522 is provided within thedelivery container 512 and is disposed opposite theside surface 512 a connected to theforward pipe line 502 or an open end of theforward pipe line 502. Thus, although the medicine introduced from theforward pipe line 502 intodelivery container 512 collide with the buffer means 522 from the force of the airflow, breakage or chipping of the medicine hardly occurs. - In the above-described
transfer device 500, theshutter 514 is in the closed state and is inclined as it awaits the transfer of the medicine. Thus, when the medicine is transferred into thedelivery container 512 and then falls on theshutter 514, a drop distance of the medicine is relatively short. Accordingly, an impact exerted to the medicine due to the drop withindelivery container 512 is small. Further, once the medicine falls on theshutter 514, the medicine slides along the surface of theshutter 514 to drop downward. Thus, after the medicine falls on theshutter 514, no impact is exerted to the medicine until the medicine is dispensed. Therefore, according to the above-described configuration, it is possible to minimize the impact exerted on the medicine transferred fromsub unit 3 tomain unit 2. - As described above, it is possible to easily sweep or maintain the internal space of the
outer container 530 or thedelivery container 512 by opening thelid 530 f provided on thetop surface 530 e of theouter container 530. Further, it is possible to divide thedelivery container 512 by removing theupper container body 524 from thelower container body 526. Accordingly, it is possible to easily sweep or maintain the inside of thedelivery container 512. - It is illustrated in the present embodiment that the openable and
closable lid 530 f is provided in theouter container 530 and thedelivery container 512 is configured to be divided. However, the outer container and the delivery container are not necessarily configured as such. Further, thedelivery container 512 is configured to be divide into two vertical members (theupper container body 524 and the lower container body 526). However, the delivery container may be divided into more members. Also, the delivery container may include an openable and closable lid in order to sweep the inside thereof, similar to theouter container 530. - Since the plurality of
exhausting holes delivery container 512 in the above-describedtransfer device 500, the airflow is exhausted in different directions from thedelivery container 512. However, in thetransfer device 500, thedelivery container 512 is disposed inside theouter container 530. The airflow exhausted from thedelivery container 512 accumulates in a space between theouter container 530 and thedelivery container 512 and is then exhausted from theexhausting part 532 separately provided in theouter container 530 through theprimary filter 534 and thesecondary filter 536. Thus, thetransfer device 500 can prevent dusts from blowing within themain unit 2. - It is illustrated in the present embodiment that the
outer container 530 for housing thedelivery container 512 or theexhausting part 532 is provided in order to prevent the airflow from being exhausted from thetransfer device 500 in different directions. However, if dust is unlikely to blow along with the exhaust of the airflow, or if the airflow may be exhausted a little from thetransfer device 500, theouter container 530 may not be provided. - In the above-described
outer container 530, theprimary filter 534 and thesecondary filter 536 are provided in theexhausting part 532. Thus, although the airflow exhausted into theouter container 530 contains dust, it is possible to prevent the dust from flowing out of theouter container 530. Further, since theprimary filter 534 with sparse meshes is disposed upstream of thesecondary filter 536 with fine meshes in the airflow flowing through theexhausting part 532, a service life of thesecondary filter 536 can be extended. Furthermore, it is illustrated in the present embodiment that theprimary filter 534 and thesecondary filter 536 with different sized meshes are provided in theexhaust part 532. However, the present invention should not be limited to such configuration. In some embodiments only one of the primary filter and the secondary filter may be provided. - As described above, in the
medicine dispensing part 510, thedelivery container 512 and theforward pipe line 502 are connected to each other through the flexiblejoint pipe 540. Thus, although a certain stress is applied to theforward pipe line 502, such stress can be absorbed or relieved by thejoint pipe 540, thereby preventing a joint portion between thedelivery container 512 and theforward pipe line 502 from damaging. Further, it is illustrated in the present embodiment that thedelivery container 512 and theforward pipe line 502 are connected to each other through thejoint pipe 540. However, the present invention should not be limited to such a configuration. Thejoint pipe 540 and thedelivery container 512 may be directly connected to each other. Further, in case a medicine transferring system is configured by connecting a pipe to another member in the same manner as thepipe line 540, theforward pipe line 403 and theexhaust pipe line 410 of the above-describedtransfer device joint pipe 540 may be interposed between a pipe and another member.Pipe line 140 or theforward pipe line 403, through which the medicine passes, may include a hard pipe for preventing the medicine from jamming in a halfway portion. Since a joint portion between a pipe and another member is apt to break because of stress, a connectingpipe 540 that is more flexible than the pipe at the joint portion between the piping and said other member may be used. - As described above, in case of employing the
transfer device 500, in addition to the transfer of the medicine from thesub unit 3 to themain unit 2, it is possible to sweep off the dust remaining within the serial medicine transfer path extending from themedicine dispensing part 510 to themedicine receiving part 511 by means of airflow produced by the operation of theblower 504. Thus, in case of employing thetransfer device 500, the medicine transfer path can be easily kept clean without performing large-scale work such as removal of theforward pipe line 502. Further, the timing of when to sweep the medicine transfer path by means of the airflow produced by the operation of theblower 504 may be appropriately set as, for example, a time after the predetermined quantity of medicine is packed, or a time when an operating means such as a separately-provided button is operated. - Further, in the present embodiment, when the medicine transfer path in the
transfer device 500 is swept by the airflow produced by the operation of theblower 504, the output of theblower 504 is set to be larger than the output during the transfer of the medicine. Thus, dust, which does not flow from the airflow produced during the transfer of the medicine, can be swept off by performing a sweeping operation. Further, the output of theblower 504 during sweeping thetransfer device 500 may not necessarily be increased. The output of theblower 504 may be equal to the output during the transfer of the medicine. Furthermore, the output of theblower 504 may be appropriately changed during sweeping. - The above-described
medicine dispensing system 1 is configured such that the medicine dispensed from the manual distributingunit 23 provided in themain unit 2 is inputted into themedicine preparing part 80 through the manual distributinghopper 91 provided below the manual distributing unit as shown inFIGS. 49 and 50 . However, it is preferred that the medicine dispensing system is configured to detect whether the medicine is normally dispensed from the manual distributingunit 23. Meanwhile, the manual distributingunit 23 has a plurality ofmeasures 90 and is configured to sequentially dispense the medicine from each of themeasures 90. Thus, when a means for detecting a dispensing state of the medicine is provided in each of themeasures 90, the structure of the manual distributingunit 23 becomes complicated. Accordingly, based on such knowledge, it is preferred that the above-describedmedicine dispensing system 1 includes a sensor capable of detecting the medicine midway in a path, through which the medicine dispensed from the manual distributingunit 23 passes. Specifically, as shown inFIGS. 49 and 50 , it is preferred that asensor 570 capable of detecting the medicine is provided in the manual distributinghopper 91 disposed between the manual distributingunit 23 and themedicine preparing part 80. - Next, other inventions will be explained hereinafter. There exists in the art a medicine dispensing device as disclosed in the below-mentioned
reference Patent Document 2. A prior art medicine dispensing device has a storage part for storing a plurality kinds of medicines. Such a prior art medicine dispensing device is constructed to pack medicines removed from the storage part according to prescriptions into a packing paper sheet at a packing part and dispense the same. (see Patent Document 2: Japanese Laid-Open Patent Application No. 2006-130307) - A prior art medicine dispensing device disclosed in the above-mentioned
Patent Document 2 includes: a packing part for packing medicines; and a packing paper sheet conveying part including a conveying means such as a conveyor for conveying the packing paper sheet, in which the medicines are packed, toward a removal opening. However, when abnormality in conveying a packing paper sheet occurs due to jamming caused by the packing paper sheet in the conveying part, the prior art device does not have a technique for rapidly and reliably detecting such abnormality. Further, in the prior art medicine dispensing device, a position of a dispensing opening for dispensing the packed medicine is determined under configuration of the conveying means and the packing part. Thus, there is a problem with the prior art device in that the packed medicine can be removed at a desired position. - Thus, there is a need for a medicine dispensing device, which is configured to rapidly and reliably detect abnormality in packing paper sheet transfer in a packing paper sheet conveying part, and a medicine dispensing system including the same. Further, there is a need to provide a medicine dispensing device and a medicine dispensing system, which are configured to remove medicine packed in a packing part at a desired position.
- In one embodiment a medicine dispensing device includes a storage part configured to store and dispense medicine; a packing part configured to pack the medicine dispensed from the storage part into a packing paper sheet; and a packing paper sheet conveying part configured to convey a packing paper sheet into which the medicine is packed by the packing part. The packing paper sheet conveying part includes: a packing paper sheet conveying means configured to convey the packing paper sheet along a predetermined conveyance path through contact with the packing paper sheet; and a detecting means configured to contact the packing paper sheet passing through the conveyance path and operate independently of the packing paper sheet conveying means. It is detected upon a condition of not operating of the detecting means during operation of the packing paper sheet conveying means whether an abnormality in transferring a packing paper sheet occurs.
- In another embodiment a medicine dispensing device includes, at the packing paper sheet conveying part, the detecting means contacting the packing paper sheet and operating independently of the packing paper sheet conveying means. The medicine dispensing device can detect whether or not the packing paper sheet transfer is normal through the detecting means. Further, the medicine dispensing device can rapidly and precisely detect an abnormality in the packing paper sheet transfer. Thus, the medicine dispensing device can perform appropriate measures such as stopping the packing paper sheet transfer, or stopping the dispensing of medicine to the packing paper sheet. Thus, it may be possible to minimize the amount of the packing paper sheet or the medicine wasted when an abnormality in the packing paper sheet transfer occurs.
- Further the detecting means may include a roller independently rotatable of the packing paper sheet conveying means; and a rotation detecting means configured to detect a rotation of the roller.
- According to such configuration, there can be provided a medicine dispensing device which can detect an abnormality in packing paper sheet transfer based on whether the rotation of the roller is detected by the rotation detecting means.
- Further, the packing paper sheet conveying part may be configured to bend the conveyance path of the packing paper sheet.
- According to such configuration, there can be provided a medicine dispensing device, which can remove the medicine packed in the packing part at a desired position by appropriately bending the conveyance path in the packing paper sheet conveying part.
- In the medicine dispensing device according to the above-described embodiment, in order to rapidly detect the abnormality in packing paper sheet transfer, an abnormality in packing paper sheet transfer can be detected in a position as far upstream as possible in a conveyance direction of the packing paper sheet where the occurrence of the abnormality in packing paper sheet transfer can be accurately detected. Specifically, the abnormality in packing paper sheet transfer can be detected in a position as far upstream as possible in the conveyance direction of the packing paper sheet where a conveyance force acts on the packing paper sheet.
- Thus, the detecting means may be situated upstream in the conveyance direction of the packing paper sheet in the packing paper sheet conveying means.
- According to such configuration, there can be provided a medicine dispensing device, which can rapidly and accurately grasp an abnormality in packing paper sheet transfer when it occurs.
- Further, the packing paper sheet conveying part may include a packing part for packing medicine. The packing paper sheet conveying means may be provided downstream in the conveyance direction of the packing paper sheet relative to the packing part. The packing paper sheet conveying means may include a receiving part receiving a packing paper sheet conveyed from the packing part; and a conveying part downstream of the conveying of the packing paper sheet received in the receiving part. The detecting means may be disposed near a boundary between the receiving part and the conveying part.
- In the medicine dispensing device, the receiving part receiving the packing paper sheet is provided in the packing paper sheet conveying means. In the conveying part, a conveyance force acts on the packing paper sheet received in the receiving part to convey the packing paper sheet. Thus, where the detecting means is disposed near the boundary between the receiving part and the conveying part, similar to the medicine dispensing device of the present invention, an abnormality in packing paper sheet transfer can be rapidly and accurately detected.
- Further, there is provided a medicine dispensing system including a main unit; one or more sub units; and a transfer device configured to connect the main unit and the sub units. The main unit includes the above-described medicine dispensing device. The sub unit includes a sub storage part configured to store and dispense a plurality kinds of medicines. The transfer device transfers the medicine dispensed from the sub storage part toward the main unit. The packing means of the main unit packs and dispenses the medicine.
- The medicine dispensing system may include the main unit and the sub unit. It is configured such that the medicine dispensed from the sub storage part provided in the sub unit is transferred to the main unit through the transfer device and is packed and dispensed together with the medicine dispensed in the main unit. However, when the packing paper sheet conveying part provided in the main unit cannot rapidly and accurately detect an abnormality in packing paper sheet transfer, the medicine dispensed in the main unit as well as the medicine dispensed in the sub unit are not allowed to be properly packed. As a result, when the medicines dispensed from both the main unit and the sub unit are allowed to be packed together as described in the medicine dispensing system of the present invention, not detecting the abnormality in packing paper sheet transfer rapidly and accurately raises problems in that the wasted amount of the packing paper sheet and the medicine becomes excessive.
- Thus, a medicine dispensing device in some embodiments may be employed as the main unit. Thus, when an abnormality in packing paper sheet transfer is detected in the main unit, such abnormality can be rapidly and accurately detected. Further, an abnormality in packing paper sheet transfer can be detected rapidly and accurately in some embodiments, the medicine dispensing device can perform appropriate measures such as stopping the packing paper sheet transfer, or stopping to dispense medicines to the packing paper sheet in case of the occurrence of an abnormality in packing paper sheet transfer. Thus, the wasted amount of the packing paper sheet and the medicine can be minimized.
- There can be provided in other embodiments, a medicine dispensing device, which is configured to rapidly and reliably detect an abnormality in packing paper sheet transfer in a packing paper sheet conveying part, and the medicine dispensing system including the same. Further, there can be provided a medicine dispensing device and a medicine dispensing system, which are configured to remove a medicine packed in the packing part at a desired position.
- Next, another embodiment will be explained hereinafter. There exists in the art a medicine dispensing device as disclosed in the below-mentioned
reference Patent Document 3. A prior art medicine dispensing device has a medicine dispensing means. Such a prior art medicine dispensing device is configured to pack medicines dispensed from the medicine dispensing means according to prescriptions into a packing paper sheet at a packing means. Further, as disclosed inPatent Document 3, the prior art medicine dispensing device includes a printing means and is configured to print necessary information such as contents of the packed medicine on the packing paper sheet through the printing means. (see Patent Document 3: Japanese Laid-Open Patent Application No. 2006-130307). - In a packing work performed by the prior art medicine dispensing device disclosed in the
Patent Document 3, pharmacists monitor whether medicines to be fed to the packing part and to be packed therein are accurately packed. The prior art medicine dispensing device disclosed in thePatent Document 3 is configured to assume that the medicines to be packed are fed to the packing part at a time when the medicines to be fed to the packing part and to be packed therein are ready and then to perform a printing operation to a packing paper sheet through the printing means. Thus, in the packing work performed by the prior art medicine dispensing device disclosed in thePatent Document 3, it cannot be judged by looking over the information printed on the packing paper sheet whether the medicines to be packed are accurately packed. Thus, it has a problem in that the examination work becomes complicated. Further, it has another problem in that the packing paper sheet, to which the printing operation is performed after the medicines are already packed, appears to be under a normally packed state. Further, in the prior art medicine dispensing device, even if the medicines to be packed are not ready due to an abnormality in feeding medicines to the packing part, the printing operation is performed to a packing paper sheet, thereby wasting the packing paper sheet. - Thus, in one embodiment a medicine dispensing device, which is configured to rapidly and precisely perform an examination work and to prevent the occurrence of wasted packing paper sheets, and a medicine dispensing system including the same.
- In one embodiment a medicine dispensing device, which includes a medicine dispensing means configured to dispense a medicine according to a prescription; a medicine preparing means configured to receive a medicine dispensed from the medicine dispensing means and to dispense the same at a predetermined time; a packing means configured to pack a medicine dispensed from the medicine preparing means into a packing paper sheet; a packing paper sheet feeding means configured to feed a packing paper sheet to the packing means; and a printing means configured to print predetermined information on a packing paper sheet fed from the packing paper sheet feeding means to the packing means. The printing means is disposed upstream of the packing means in a flow direction of the packing paper sheet fed by the packing paper sheet feeding means. A length of a path, through which a packing paper sheet passes between the printing means and the packing means, is n times the length of a packing paper sheet necessary for packing a medicine for one pack. The medicine preparing means includes a plurality of sections configured to gather the medicine dispensed from the medicine dispensing means for one pack respectively and is configured to dispense the medicines gathered in the plurality of sections in a predetermined order. The printing means prints information corresponding to a section A of the plurality of sections on the packing paper sheet at a time earlier by a time period necessary for dispensing medicine for a section n from the medicine preparing means than a timing of dispensing a medicine gathered in section A.
- In another embodiment, the length of the path, through which the packing paper sheet passes between the printing means and the packing means, is set to be n times the length of the packing paper sheet necessary for packing medicine for one pack. Further, the medicine preparing means includes a plurality of sections and is configured to dispense the medicine gathered in each of the sections in a predetermined order. Thus, the medicine dispensed from section A is packed into the packing paper sheet, which the printing means prints at a time earlier by a time period necessary for dispensing a medicine for the section n (i.e., equal to n packs) from the medicine preparing means toward the packing means than a time for dispensing a medicine gathered in the section A. That is, a medicine to be packed is supplied to section A at a time prior to performing the print operation corresponding to section A to the packing paper sheet. Further, a timing when the medicine gathered in the section A is dispensed to the packing part and a timing when a section of a packing paper sheet with the information corresponding to section A printed thereon reaches the packing part are coincidental. Thus, the medicine dispensing device of the present invention performs printing to a packing paper sheet when medicine to be packed is supplied to section A. Further, it can easily monitor whether or not a medicine to be packed is exactly supplied and resolve the waste of a packing paper sheet resulting from an abnormality in feeding a medicine.
- Further, in the above-described medicine dispensing device, a printing operation to the packing paper sheet may be performed by the printing means upon a condition that the medicine is fed into section A up to a time earlier by the time period necessary for dispensing a medicine for the section n from the medicine preparing means than the time of dispensing a medicine gathered in the section A of the plurality of sections in the medicine preparing means.
- Further, in the above-described medicine dispensing device, the medicine is dispensed from the medicine dispensing means to section A at a time earlier by a time period more than the time period necessary for dispensing a medicine for the section n from the medicine preparing means than the time of dispensing a medicine gathered in section A in the medicine preparing means. Thus, the information corresponding to section A is printed on the packing paper sheet after the medicine is fed into section A. Thus, the medicine dispensing device can easily monitor whether or not a medicine to be packed is accurately packed and resolve the waste of a packing paper sheet resulting from an abnormality in feeding a medicine.
- Further a medicine dispensing device includes a medicine dispensing means configured to dispense a medicine according to a prescription; a medicine preparing means configured to receive a medicine dispensed from the medicine dispensing means and to dispense the same at a predetermined time; a packing means configured to pack a medicine dispensed from the medicine preparing means into a packing paper sheet; a packing paper sheet feeding means configured to feed a packing paper sheet to the packing means; and a printing means configured to print predetermined information on a packing paper sheet fed from the packing paper sheet feeding means to the packing means. The printing means is disposed upstream of the packing means in a flow direction of the packing paper sheet fed by the packing paper sheet feeding means. The medicine preparing means includes a plurality of sections configured to gather the medicine for one pack dispensed from the medicine dispensing means respectively. The medicine preparing means is configured to dispense the medicines gathered in the plurality of sections in a predetermined order. A medicine is dispensed from the medicine dispensing means into one section A of the plurality of sections at a time earlier by a timing Z as early as a time period Y when the packing paper sheet fed by the packing paper sheet feeding means moves from a position corresponding to the printing means to the packing means, than a timing X when the medicine in the section A is dispensed from the medicine dispensing means toward the packing means. Information corresponding to section A is printed on the packing paper sheet at the time Z by the printing means.
- In the above-described medicine dispensing device, medicine is fed into section A of the medicine preparing means at a time earlier than the time Z. Further, the information corresponding to section A is printed on the packing paper sheet by the printing means at the time Z as early as the time period Y when the packing paper sheet fed by the packing paper sheet feeding means moves from the position corresponding to the printing means to the packing means, from the timing X when the medicine in section A is dispensed from the medicine dispensing means toward the packing means. That is, the information corresponding to section A is printed on a portion of the packing paper sheet, which is used for packing the medicine in section A, at the same time as, or later than a time for feeding the medicine into section A. Thus, the medicine dispensing device can perform the printing operation to the medicine dispensing device after ascertaining that the medicine to be packed is exactly fed into the section. Further, the medicine dispensing device can easily monitor whether or not the medicine to be packed is exactly fed and resolve the waste of a packing paper sheet resulting from an abnormality in feeding a medicine.
- Further, the printing operation to the packing paper sheet may be performed upon a condition that the medicine is fed into section A at a time earlier than the time Z.
- With such configuration, if the printing operation to the packing paper sheet is not performed, it can be judged that the medicine is not fed exactly before the time Z. Thus, examining whether or not the medicine is exactly packed can become easy. Further, according to such configuration, if the medicine is not fed into the section A before the time Z, the printing operation to the packing paper sheet stops, thereby preventing the occurrence of the wasted packing paper sheet in advance.
- Further, a print purporting that the medicine to be packed runs short may be made on the packing paper sheet by the printing means upon a condition that the medicine to be packed is not inputted to section A until the time earlier than the time Z.
- According to such configuration, it is ascertained through only looking over the print made on the packing paper sheet that the medicine to be packed runs short. Thus, the examination work can be performed more easily and reliably.
- Further, in the above-described medicine dispensing device, the medicine preparing means may include a section forming body having a plurality of sections arranged circumferentially; and a dispensing opening. The section forming body may be configured to move relative to the dispensing opening. When the section reaches a position corresponding to the dispensing opening, the medicine gathered in the section may be disposed through the dispensing opening.
- Further, there is provided a medicine dispensing system that includes a main unit; one or more sub units; and a transfer device configured to connect the main unit and the sub units. The main unit includes the above-described medicine dispensing device. The sub unit includes a sub storage part configured to store and dispense a plurality kinds of medicines. The transfer device transfers the medicine dispensed from the sub storage part toward the main unit and feeds the medicine into the section provided in the medicine preparing means. The packing part of the main unit packs and dispenses the medicine.
- The medicine dispensing system includes the main unit and the sub unit. It is configured such that the medicine dispensed in the sub unit is transferred to the medicine preparing means provided in the main unit and is packed and dispensed together with the medicine dispensed in the main unit by the packing means. However, in the medicine dispensing system, there is a possibility that an abnormality in dispensing medicine to the medicine preparing means occurs in the main unit. In addition, there is another possibility that an abnormality in dispensing medicine occurs in the sub unit, and that troubles take place during transferring a medicine to the medicine preparing means through the transfer device. As such, where the main unit is provided, the medicine dispensing system may have many factors associated with the abnormality in dispensing medicine to the medicine preparing means. Accordingly, similar to the above-described medicine dispensing device of the present invention, it is preferred that the above-described medicine dispensing system may have some means so that it can easily monitor whether a packing operation is accurately performed and prevent the packing paper sheet from wasting concomitantly with the abnormality in dispensing a medicine to the medicine preparing means.
- Thus, the medicine dispensing system, which is provided based on such knowledge, employs the above-described medicine dispensing device as the main unit. Thus, the medicine dispensing system can prevent the packing paper sheet from being wasting in conjunction with an abnormality in dispensing a medicine to the medicine preparing means.
- According to another embodiment, there can be provided a medicine dispensing device, which is configured to easily and accurately perform the examination work regarding whether or not packing medicine is accurately performed and to prevent the packing paper sheet from wasting even if the medicine to be dispensed becomes unready due to an abnormality in feeding a medicine to the packing part. Further, there can be provided a medicine dispensing system that includes such a medicine dispensing device.
- Next, another embodiment will be explained hereinafter. There exists in the art a medicine dispensing device as disclosed in the below-mentioned
reference Patent Document 4. A prior art medicine dispensing device includes a plurality of medicine feeding containers configured to store medicine in a storage part and dispense the medicine. Such a prior art medicine dispensing device is configured to dispense the medicine from each of the medicine feeding container by the amount corresponding to a prescription and pack the same. (see Patent Document 4: Japanese Laid-Open Patent Application No. 2001-276183). - The prior art medicine dispensing device is used in such a manner that each of the medicine feeding containers accommodates different kinds of medicines. However, the prior art medicine dispensing device is not configured to simply and accurately grasp characteristic data of each medicine feeding container, such as a date and time when the medicine feeding container is filled with medicines, a user filling the medicine feeding container, data related to medicines accommodated in the medicine feeding container, etc. Further, as the number of the medicine feeding containers increases with an increase in the kinds of medicines to be dealt with, such a tendency becomes strong. Thus, the relevant art requires a medicine dispensing device configured to simply and accurately grasp characteristic data of each medicine feeding container. Similarly, a medicine dispensing system, which is constructed by combining a plurality of medicine dispensing devices, is required to be configured to simply and accurately grasp characteristic data of each medicine feeding container.
- Thus, to satisfy the aforementioned demand, it is an object of the present invention to provide a medicine dispensing device and a medicine dispensing system, which are configured to simply and accurately grasp characteristic data of each medicine feeding container.
- In on embodiment a medicine dispensing device, which includes a medicine feeding container configured to store a medicine, the medicine feeding container including an information recordable medium; a container mounting part configured to mount the medicine feeding container; and a control means. The medicine is allowed to be dispensed by mounting the medicine feeding container to the container mounting part. The control means is configured to perform data communication for a characteristic data of the medicine feeding container with the information recordable medium of the medicine feeding container.
- According to such configuration, there can be provided a medicine dispensing device, which can perform the data communication for the characteristic data between the control means and the medicine feeding container having the information recordable medium and can simply and accurately grasp the characteristic data.
- Further, a medicine dispensing device, which is provided based on the same knowledge, may include a storage means configured to store and dispense medicine; and a control means configured to data-communicate with an information recordable medium. The storage means may include a plurality of attachable/detachable medicine feeding containers configured to store and dispense the medicine. The information recordable medium may be provided in some or all of the medicine feeding containers. A data communication for the characteristic data of the medicine feeding container may be performed between the information recordable medium of the medicine feeding container and the control means.
- The above-described medicine dispensing device includes a storage means configured to store and dispense medicine; and a control means configured to data-communicate with the information recordable medium. Herein, the storage means includes a shelf or drum, in which a plurality of medicine feeding container are removably provided (for example, this may be referred to as a main storage part or a sub storage part in embodiments described below). Further, in the medicine dispensing device, a plurality of medicine feeding containers configured to store and dispense a medicine are removably provided in the storage means, which includes a shelf or drum. Herein, the medicine feeding container corresponds to a feeder container in the below-described embodiments and a container capable of dispensing the medicine accommodated therein. The above-described storage means, which includes the medicine feeding container, can dispense the medicine dispensed from the medicine feeding container for the purpose of packing the same.
- With the above-described constitution, there can be provided a medicine dispensing device, which can data communicate with the control means with respect to the characteristic data of each of the medicine feeding containers with the information recordable medium and thus can simply and accurately grasp the characteristic data.
- Further, the control means may be configured to data communicate with an operator information recordable medium recording an operator information specifying an operator. The operator information read from the operator information recordable medium through the data communication may be recorded into the information recordable medium.
- According to such constitution, information on an operator, who performs tasks relevant to the medicine feeding container, such as filling the medicine feeding container with medicines, may be recorded into the information recordable medium of each of the medicine feeding containers.
- Further, the medicine dispensing device may be configured to operate in a plurality of operation modes. The operation mode may change in a predetermined operation mode selected from a plurality of operation modes upon a condition that the data communication is allowed between the control means and the information recordable medium of the medicine feeding container removed from a container mounting part.
- In the medicine dispensing device, the operation mode changes upon a condition that the data communication is allowed between the control means and the information recordable medium of the medicine feeding container. That is, it can be used as a trigger for changing the operation modes that the information recordable medium provided in each of medicine feeding container is allowed to data communicate with the control means. Thus, efforts required to change the operation modes can be minimized and misoperation can be prevented.
- Further, the medicine dispensing device may include a mark reading means for reading an identification mark assigned to each of the kinds of medicine. The kinds of medicine may be specified by the control means based on the identification mark read by the mark reading means. Information on the kinds of medicine may be recorded into the information recordable medium through data communication between the control means and the information recordable medium of the medicine feeding container removed from the container mounting part.
- According to such configuration, if the mark reading means reads the identification mark assigned to each of the kinds of medicine when filling the medicine feeding container removed from the container mounting part with a medicine, the information on the kind of such a medicine can be recorded into the information recordable medium of the medicine feeding container through data communication. Thus, according to the medicine dispensing device of one embodiment, when the medicine feeding container is filled with a medicine, the information on the kinds of medicine can be easily and reliably recorded into the information recordable medium.
- Further, the medicine dispensing device according to the above-described invention may further include a cassette placing part configured to place the medicine feeding container removed from the container mounting part; and an interface means wiredly or wirelessly connected to the control means. When the medicine feeding container is placed on the cassette placing part, the information recordable medium of the medicine feeding container may be allowed to data communicate with the control means via the interface means.
- According to such configuration, efforts required to enable the data communication between the information recordable medium and the control means after removing the medicine feeding container from the container mounting part can be minimally saved.
- Further, the medicine dispensing device may further include an interface means wiredly or wirelessly connected to the control means. The interface means may be configured to read and record data as not in contact with the information recordable medium.
- According to such configuration, efforts required to enable the data communication between the information recordable medium and the control means after removing the medicine feeding container from the container mounting part can be saved.
- The above-described medicine dispensing device can data-communicate with the information recordable medium of each of the medicine feeding containers with respect to the characteristic data of the medicine feeding container. Thus, the medicine dispensing device can be configured to dispense medicines for purposes of packing the same even if the medicine feeding container accommodating a predetermined medicine is situated at any location in the storage means. However, some medicine of the plurality kinds of medicines is prone to bound, roll over, break or chip due to drop impact at a dispensing portion while dispensed from the medicine feeding container. In case of dealing with such a medicine, it must be dealt with in a different manner from those for other medicines (for example, adjustment in dispensing timing regarding bound or roll, means for mitigating drop impact, etc.) so as not to cause an abnormality in dispensing medicine. Accordingly, the medicine feeding container accommodating medicine having such a particular characteristics is attached to a location capable of resolving the foregoing matter.
- Thus, based on such knowledge, medicines may be sequentially dispensed based on prescription data inputted to the control means. A plurality of the container mounting parts configured to mount the medicine feeding container may be provided. The control means may include a correspondence relationship storing part defining and storing a correspondence relationship between the plurality of container mounting parts and the medicine feeding container to be attached to the plurality of the container mounting parts; and a judging part. The judging part may be configured to perform an error judgment operation for judging the following states, by comparing the correspondence relation storing part and the characteristic data of the medicine feeding container obtained from the data communication with the information recordable medium of the medicine feeding container mounted on the container mounting part: a right mount state where the medicine feeding container is properly mounted on the container mount part coinciding with the correspondence relationship regulated in the correspondence relationship storing part; and an erroneous mount state where the medicine feeding container is erroneously mounted on the container mounting part against the correspondence relationship regulated in the correspondence relationship storing part. Dispensing the medicines may continue from other medicine feeding containers excluding a erroneously mounted medicine feeding container upon a condition that it is judged by the error judgment operation that there is an erroneously mounted medicine feeding container, and that a medicine accommodated in the erroneously mounted medicine feeding container is not medicine to be dispensed according to the prescription data. Dispensing the medicines may stop upon a condition that it is judged by the error judgment operation that there is the erroneously mounted medicine feeding container, and that a medicine accommodated in the erroneously mounted medicine feeding container is a medicine to be dispensed according to the prescription data.
- In the medicine dispensing device of one embodiment, the judging part of the control means performs an error judgment operation. Based on the correspondence relationship between the container mounting part and the medicine feeding container, which is regulated in the correspondence relationship storing part, it can be judged whether the medicine feeding container is properly mounted or erroneously mounted on the container mounting part dedicated for said medicine feeding container. Further, in the medicine dispensing device, where the medicine feeding container is erroneously mounted and such a medicine feeding container does not accommodate a medicine to be dispensed, even if dispensing a medicine does not intentionally stop in other medicine feeding containers, problems such as bound, roll, breakage, chipping, etc. of medicines do not occur. And, stopping to dispense a medicine leads to loss of work efficiency. Accordingly, in the medicine dispensing device, where the erroneously mounted medicine feeding container does not accommodate a medicine to be dispensed, dispensing a medicine continues and the erroneously mounted medicine feeding container can be dismounted without stopping to dispense medicine. Accordingly, in the medicine dispensing device, even if the erroneously mounted medicine feeding container exists, the loss of work efficiency resulting therefrom can be minimized.
- By contrast, where the erroneously mounted medicine feeding container exists and such a medicine feeding container accommodates a medicine to be dispensed, continuing to dispense a medicine causes the aforementioned problems such as bound, roll, breakage, chipping, etc. of medicines. Accordingly, in such a case, the medicine dispensing device of in some embodiments is configured to stop to dispense a medicine. Thus, according to the medicine dispensing device in some embodiments, it is possible to prevent medicines from being dispensed from the erroneously mounted medicine feeding container.
- Further, it is preferred that medicines prone to bound, roll over, break or chip due to drop impact at the dispensing portion are dispensed at a side as low as possible.
- Thus, in the above-described medicine dispensing device provided based on such knowledge, the storage means may include a plurality of the container mounting parts configured to mount the medicine feeding container. The container mounting parts may be vertically arranged. It may be judged through the error judgment operation whether a medicine feeding container to be mounted on a container mounting part provided below a predetermined height is erroneously mounted on a container mounting part provided in a position above the predetermined height.
- According to such configuration, it can be prevented that the medicine feeding container accommodating the medicine to be dispensed at a side as low as possible (i.e. the aforementioned medicine causing problems such as bound, roll, breakage or chipping concomitantly with drop) is erroneously mounted on the container mounting part situated in a position above the predetermined height.
- Further, the above-described medicine dispensing device provided based on the same knowledge, the container mounting part configured to mount the medicine feeding container may be disposed in each of a plurality of container mounting regions defined along a height direction. The correspondence relationship storing part may regulate the correspondence relationship between the container mounting part and the medicine feeding container to be attached to the container mounting part as a relationship relative to the container mounting region located at a height corresponding to an upper attachment limit of a medicine feeding container that is determined according to a kind of medicine. The erroneous mount state may be judged through the error judgment operation when a medicine feeding container is mounted on a container mounting part of a container mounting region locating beyond a container mounting region located at a height corresponding to the upper attachment limit. The right mount state may be judged through the error judgment operation when a medicine feeding container is mounted on a container mounting part of a container mounting region located at a height below the upper attachment limit.
- In the medicine dispensing device, the correspondence relationship storing part can regulate the correspondence relationship between the container mounting regions and the height corresponding to the upper attachment limit of the medicine feeding container at a plurality of steps in view of that bound, roll, breakage or chipping occurs at what level concomitantly with drop. Further, the erroneous mount state can be judged through the error judgment operation based on such a regulation, when a medicine feeding container is mounted on a container mounting part of a container mounting region located upward beyond a container mounting region located at a height corresponding to the upper attachment limit. Thus, it is possible to prevent the occurrence of trouble such as an abnormality in dispensing a medicine resulting from the erroneous mount state.
- Further, the control means may be configured to perform a search operation for searching and selecting a container mounting part, on which the medicine feeding container judged to be in the erroneous mount state through the error judgment operation must be mounted.
- According to such configuration, it can be easily determined through the search operation on which container mounting part the erroneously mounted medicine feeding container must be mounted.
- Further, a search condition may be determined based on the characteristic data of the medicine feeding container obtained by the data communication with the information recordable medium, which the medicine feeding container judged to be in the erroneous mount state through the error judgment operation includes.
- According to such configuration, even if an operator does not separately input a search condition in the search operation, the container mounting part on which the erroneously mounted medicine feeding container must be mounted can be selected. Thus, convenience in the search operation can be enhanced.
- In the above-described invention, the storage means may be configured to move each of the container mounting parts to an attachment/detachment work position where an attachment/detachment work of the medicine feeding container can be performed. The container mounting part selected through the search operation may be moved to the attachment/detachment work position.
- In such a medicine dispensing device, a container mounting part located at a proper position, in which the erroneously mounted medicine feeding container must be properly attached, is moved to the attachment/detachment work position. Thus, convenience in attaching the medicine feeding container in the proper position can be enhanced.
- Further, there is provided a medicine dispensing system that includes a main unit; one or more sub units; and a transfer device configured to connect the main unit and the sub units. The main unit includes the above-described medicine dispensing device. The sub unit includes a sub storage means configured to store and dispense a plurality kinds of medicines. The sub storage means includes a plurality of attachable/detachable medicine feeding containers configured to store and dispense a medicine. The transfer device transfers the medicine dispensed from the sub storage means toward the main unit. The medicine is dispensed in the main unit.
- Such a medicine dispensing system includes the main unit and the sub unit. A plurality of medicine feeding containers are removably attached to both the storage means of the main unit and the sub storage means of the sub unit. Accordingly, the medicine dispensing system has a large number of medicine feeding containers and thus needs to be configured to even more easily and reliably control the characteristic data of each of the medicine feeding containers. Thus, the medicine dispensing system, which is provided based on such knowledge, includes the above-described medicine dispensing device as the main unit. As a result, the medicine dispensing system can simply and accurately grasp and control the characteristic data through the data communication between the control means provided in the main unit and the information recordable medium of each of the medicine feeding containers provided in the main unit and the sub unit.
- Thus, there can be provided a medicine dispensing device and a medicine dispensing system, which are configured to simply and accurately grasp the characteristic data of each medicine feeding container.
Claims (24)
1. A medicine dispensing device comprising:
a medicine feeding container configured to store a medicine;
a container mounting part configured to mount the medicine feeding container thereon;
a cassette placing part configured to place the medicine feeding container thereon;
a control means; and
an interface means wiredly or wirelessly connected to the control means,
wherein the medicine is allowed to be dispensed by mounting the medicine feeding container to the container mounting part,
wherein the medicine feeding container includes an information recordable medium to which a characteristic container information on the medicine feeding container is recordable,
wherein when the medicine feeding container is placed on the cassette placing part, a data communication between the control means and the information recordable medium of the medicine feeding container is allowed via the interface means, and
wherein when the medicine feeding container is mounted on the container mounting part, a data communication between the control means and the information recordable medium is allowed via the interface means.
2. The medicine dispensing device of claim 1 , wherein when the medicine feeding container is placed on the cassette placing part, the characteristic container information on the medicine feeding container is read by the control means and the characteristic container information is displayed.
3. The medicine dispensing device of claim 1 , wherein the medicine dispensing device is operable in a general operation mode for dispensing medicines according to a prescription and in a medicine filling mode for filling the medicine feeding container with medicines, and
wherein when the medicine feeding container removed from the container mounting part is placed on the cassette placing part, the medicine dispensing device is changed from the general operation mode to the medicine filling mode.
4. The medicine dispensing device of claim 1 , further comprising a mark reading means configured to read an identification mark assigned per kinds of medicine,
wherein the kinds of medicine is specified by the control means based on the identification mark read by the mark reading means, and
wherein an information on the kinds of medicine is recorded into the information recordable medium through the data communication between the control means and the information recordable medium of the medicine feeding container.
5. The medicine dispensing device of claim 1 , wherein a dispensing history of the medicine in the medicine feeding container is recorded into the information recordable medium by the control means while the medicine feeding container is mounted on the container mounting part.
6. The medicine dispensing device of claim 1 , wherein the characteristic container information includes a data on a usage history of the medicine feeding container, and
wherein, based on the data on the usage history, the control means judges whether the medicine feeding container reaches a durable term and/or a maintenance time.
7. The medicine dispensing device of claim 1 , wherein another device provided separately accesses the information recordable medium and reads and writes a data from and into the information recordable medium.
8. The medicine dispensing device of claim 1 , wherein medicines are sequentially dispensed based on a prescription data inputted to the control means,
wherein a plurality of the container mounting parts configured to mount the medicine feeding container are provided,
wherein the control means comprises:
a correspondence relationship storing part regulating and storing a correspondence relationship between the plurality of the container mounting parts and the medicine feeding container to be attached to the plurality of the container mounting parts; and
a judging part,
wherein the judging part is configured to perform an error judgment operation for judging the following states, by comparing the correspondence relation storing part and the characteristic data of the medicine feeding container obtained from the data communication with the information recordable medium of the medicine feeding container mounted on the container mounting part:
a right mount state where the medicine feeding container is properly mounted on the container mount part coinciding with the correspondence relationship regulated in the correspondence relationship storing part; and
an erroneous mount state where the medicine feeding container is erroneously mounted on the container mounting part against the correspondence relationship regulated in the correspondence relationship storing part,
wherein dispensing the medicines continues through other medicine feeding containers excluding a erroneously mounted medicine feeding container upon a condition that it is judged by the error judgment operation that there is the erroneously mounted medicine feeding container, and that a medicine accommodated in the erroneously mounted medicine feeding container is not a medicine to be dispensed according to the prescription data, and
wherein dispensing the medicines stops upon a condition that it is judged by the error judgment operation that there is the erroneously mounted medicine feeding container, and that a medicine accommodated in the erroneously mounted medicine feeding container is a medicine to be dispensed according to the prescription data.
9. The medicine dispensing device of claim 8 , wherein the container mounting part configured to mount the medicine feeding container is disposed in each of a plurality of container mounting regions defined along a height direction,
wherein the correspondence relationship storing part regulate the correspondence relationship between the container mounting part and the medicine feeding container to be attached to the container mounting part as a relationship relative to the container mounting region located at a height corresponding to an upper attachment limit of a medicine feeding container that is determined according to the kinds of medicine,
wherein the erroneous mount state is judged through the error judgment operation when the medicine feeding container is mounted on a container mounting part of a container mounting region locating above a container mounting region located at the height corresponding to the upper attachment limit, and
wherein the right mount state is judged through the error judgment operation when the medicine feeding container is mounted on a container mounting part of a container mounting region located at a height equal to or lower than the upper attachment limit.
10. The medicine dispensing device of claim 8 , wherein the control means is configured to perform a search operation for searching and selecting a container mounting part, on which the medicine feeding container judged to be in the erroneous mount state through the error judgment operation is mounted.
11. The medicine dispensing device of claim 10 , wherein a search condition in the search operation is determined based on the characteristic data of the medicine feeding container obtained by the data communication with the information recordable medium, which the medicine feeding container judged to be in the erroneous mount state through the error judgment operation includes.
12. The medicine dispensing device of claim 10 , wherein each of the container mounting parts is movable to an attachment/detachment work position where an attachment/detachment work of the medicine feeding container is performed, and
wherein the container mounting part selected through the search operation is moved to the attachment/detachment work position.
13. A medicine dispensing device comprising:
a medicine feeding container configured to store a medicine;
a container mounting part configured to mount the medicine feeding container thereon;
a cassette placing part configured to place the medicine feeding container thereon;
a control means; and
an interface means provided in each of the container mounting part and the cassette placing part, the interface means being wiredly or wirelessly connected to the control means,
wherein the medicine is allowed to be dispensed by mounting the medicine feeding container to the container mounting part,
wherein the medicine feeding container includes an information recordable medium to which a characteristic container information on the medicine feeding container is recordable,
wherein when the medicine feeding container is mounted on the container mounting part, a data communication between the control means and the information recordable medium is allowed via the interface means, and
wherein when the medicine feeding container removed from the container mounting part is placed on the cassette placing part for filling the medicine feeding container with a medicine, a data communication between the control means and the information recordable medium of the medicine feeding container is allowed via the interface means and thus the characteristic container information including a data on the medicine is grasped by the control means and the characteristic container information is allowed to be renewed and recorded.
14. The medicine dispensing device of claim 13 , wherein when the medicine feeding container is placed on the cassette placing part, the characteristic container information on the medicine feeding container is read by the control means and the characteristic container information is displayed.
15. The medicine dispensing device of claim 13 , wherein the medicine dispensing device is operable in a general operation mode for dispensing medicines according to a prescription and in a medicine filling mode for filling the medicine feeding container with medicines, and
wherein when the medicine feeding container removed from the container mounting part is placed on the cassette placing part, the medicine dispensing device is changed from the general operation mode to the medicine filling mode.
16. The medicine dispensing device of claim 13 , further comprising a mark reading means configured to read an identification mark assigned per kinds of medicine,
wherein the kinds of medicine is specified by the control means based on the identification mark read by the mark reading means, and
wherein an information on the kinds of medicine is recorded into the information recordable medium through the data communication between the control means and the information recordable medium of the medicine feeding container.
17. The medicine dispensing device of claim 13 , wherein a dispensing history of the medicine in the medicine feeding container is recorded into the information recordable medium by the control means while the medicine feeding container is mounted on the container mounting part.
18. The medicine dispensing device of claim 13 , wherein the characteristic container information includes a data on a usage history of the medicine feeding container, and
wherein, based on the data on the usage history, the control means judges whether the medicine feeding container reaches a durable term and/or a maintenance time.
19. The medicine dispensing device of claim 13 , wherein another device provided separately accesses the information recordable medium and reads and writes a data from and into the information recordable medium.
20. The medicine dispensing device of claim 13 , wherein medicines are sequentially dispensed based on a prescription data inputted to the control means,
wherein a plurality of the container mounting parts configured to mount the medicine feeding container are provided,
wherein the control means comprises:
a correspondence relationship storing part regulating and storing a correspondence relationship between the plurality of the container mounting parts and the medicine feeding container to be attached to the plurality of the container mounting parts; and
a judging part,
wherein the judging part is configured to perform an error judgment operation for judging the following states, by comparing the correspondence relation storing part and the characteristic data of the medicine feeding container obtained from the data communication with the information recordable medium of the medicine feeding container mounted on the container mounting part:
a right mount state where the medicine feeding container is properly mounted on the container mount part coinciding with the correspondence relationship regulated in the correspondence relationship storing part; and
an erroneous mount state where the medicine feeding container is erroneously mounted on the container mounting part against the correspondence relationship regulated in the correspondence relationship storing part,
wherein dispensing the medicines continues through other medicine feeding containers excluding a erroneously mounted medicine feeding container upon a condition that it is judged by the error judgment operation that there is the erroneously mounted medicine feeding container, and that a medicine accommodated in the erroneously mounted medicine feeding container is not a medicine to be dispensed according to the prescription data, and
wherein dispensing the medicines stops upon a condition that it is judged by the error judgment operation that there is the erroneously mounted medicine feeding container, and that a medicine accommodated in the erroneously mounted medicine feeding container is a medicine to be dispensed according to the prescription data.
21. The medicine dispensing device of claim 20 , wherein the container mounting part configured to mount the medicine feeding container is disposed in each of a plurality of container mounting regions defined along a height direction,
wherein the correspondence relationship storing part regulate the correspondence relationship between the container mounting part and the medicine feeding container to be attached to the container mounting part as a relationship relative to the container mounting region located at a height corresponding to an upper attachment limit of a medicine feeding container that is determined according to the kinds of medicine,
wherein the erroneous mount state is judged through the error judgment operation when the medicine feeding container is mounted on a container mounting part of a container mounting region locating above a container mounting region located at the height corresponding to the upper attachment limit, and
wherein the right mount state is judged through the error judgment operation when the medicine feeding container is mounted on a container mounting part of a container mounting region located at a height equal to or lower than the upper attachment limit.
22. The medicine dispensing device of claim 20 , wherein the control means is configured to perform a search operation for searching and selecting a container mounting part, on which the medicine feeding container judged to be in the erroneous mount state through the error judgment operation is mounted.
23. The medicine dispensing device of claim 22 , wherein a search condition in the search operation is determined based on the characteristic data of the medicine feeding container obtained by the data communication with the information recordable medium, which the medicine feeding container judged to be in the erroneous mount state through the error judgment operation includes.
24. The medicine dispensing device of claim 22 , wherein each of the container mounting parts is movable to an attachment/detachment work position where an attachment/detachment work of the medicine feeding container is performed, and
wherein the container mounting part selected through the search operation is moved to the attachment/detachment work position.
Priority Applications (2)
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US14/717,966 US9833384B2 (en) | 2007-10-23 | 2015-05-20 | Medicine dispensing system and medicine dispensing device |
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JP2007274932A JP5224167B2 (en) | 2007-10-23 | 2007-10-23 | Drug dispensing apparatus and drug dispensing system |
JP2007274931 | 2007-10-23 | ||
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JP2008240590A JP2009119246A (en) | 2007-10-23 | 2008-09-19 | Drug delivery device, and drug delivery system |
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US12/765,741 US8234838B2 (en) | 2007-10-23 | 2010-04-22 | Medicine dispensing system and medicine dispensing device |
US13/364,210 US20120130532A1 (en) | 2007-10-23 | 2012-02-01 | Medicine dispensing system and medicine dispensing device |
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US14/717,966 Active US9833384B2 (en) | 2007-10-23 | 2015-05-20 | Medicine dispensing system and medicine dispensing device |
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