JP5682786B2 - Dispensing audit system - Google Patents

Description

  The present invention relates to a plurality of drug names or a plurality of drug names with information on the number of packaging units versus weight, which indicates the relationship between the number of packaging units and the weight, which is the number of drugs in a packaging unit packaged in a packaging material. Storage means for storing the corresponding medicine codes in association with each other, prescription information input means for inputting prescription information including the name and prescription quantity of the prescribed prescription medicine, and packaging in the packaging material based on the prescription information An examination table on which a drug assembly in which the drugs are collected in a state of being placed is placed as a drug to be dispensed, an imaging unit for imaging the drug assembly placed on the examination table, and imaging information of the imaging unit Based on the above, drug name determination means for determining the drug name of the drug assembly placed on the examination table, weighing means for weighing the weight of the drug assembly placed on the examination table, Input by prescription information input means Based on the prescription information, the number-of-packaging unit-weight relationship information stored in the storage unit, the drug name determination result by the drug name determination unit, and the weighing data of the weighing unit, the drug name of the drug assembly and The present invention relates to a dispensing inspection system provided with dispensing suitability determination means for determining the suitability of dispensing contents including the quantity of medicines, and determination result output means for outputting a determination result by the dispensing suitability determination means.

Such a dispensing audit system is such that a dispensing operator (such as a pharmacist), for example, refers to a prescription, and the drug name and quantity of the drug dispensed based on the prescription information match the content of the prescription information in the prescription. This is to determine whether or not.
In other words, since various forms of drugs such as tablets, capsules, powders, etc. are packaged in a packaging material, the dispensing operator collects drugs in a packaged condition in a packaging material based on prescription information. As a body, you will collect drugs. Here, the drug assembly is a group of one type of drug packaged individually, and when there are a plurality of types of prescription drugs, a plurality of types of drugs corresponding to the plurality of types of prescription drugs are used. Aggregates will be collected.
By the way, the packaging material for packaging the medicine is a sheet-like packaging material such as a PTP (Press Through Package) sheet that is packaged in a form in which a plurality of tablets or capsules are housed in a dome-shaped housing part one by one, and There is a seal wrapping material that wraps a granular or fine powder powder in a form in which a predetermined amount is stored in a bag-shaped storage portion.

The storage means includes a plurality of drug names or a plurality of drug names indicating information on the relationship between the number of packaging units and the weight, which is the number of drugs in the packaging unit packaged in the packaging material, and the weight. Is stored in association with each of the medicine codes corresponding to.
When the dispensing operator places the medicine assembly on the examination table, the imaging means picks up the medicine assembly placed on the examination table, and the medicine name discrimination means examines based on the imaging information of the imaging means. The drug name of the drug assembly placed on the table is discriminated, and the weight of the drug assembly placed on the examination table is weighed by the weighing means.
Then, the prescription information input by the prescription information input means by the dispensing suitability determination means, the number-of-packaging unit-weight relationship information stored in the storage means, the drug name determination result by the drug name determination means, and the weighing means Based on the weighing data, the suitability of the dispensing contents including the drug name of the drug assembly and the quantity of the drug is determined, and the determination result is output to the determination result output means.

In such a dispensing audit system, conventionally, the medicine name discriminating unit is configured to be able to discriminate the drug name of a single type of drug assembly based on the imaging information of the imaging unit, and the dispensing propriety determination The means is configured to determine the suitability of the dispensing contents for a single type of drug assembly, and is configured to perform a dispensing audit for the single type of drug assembly (see, for example, Patent Document 1). ).
Therefore, when a plurality of types of drugs are prescribed, the dispensing operator collects a plurality of types of drug aggregates corresponding to the plurality of types of prescription drugs, and places the drug aggregates on the examination table for each type. The suitability of the contents of dispensing will be determined.

JP 2005-279228 A

  However, in the conventional dispensing audit system, when there are a plurality of types of drug assemblies dispensed based on prescription information, the suitability of the content of dispensing must be determined by placing the drug assembly on the examination table for each type. Therefore, there is a problem that the dispensing auditing work is complicated and the dispensing auditing work takes time. Therefore, the efficiency of the dispensing auditing work is poor, and there is room for improvement in improving the efficiency.

  The present invention has been made in view of such circumstances, and an object of the present invention is to provide a dispensing audit system capable of improving the efficiency of dispensing auditing work.

The dispensing inspection system according to the present invention provides the number of packaging units versus weight relationship information indicating the relationship between the number of packaging units and the weight, which is the number of medicines in the packaging unit in a state of being packaged with a packaging material. Based on the prescription information, storage means for storing the medicine code corresponding to each medicine name in association with each other, prescription information input means for inputting prescription information including the name and prescription quantity of the prescribed prescription medicine An inspection table on which a drug assembly in which the drugs are collected while being packaged in a packaging material is placed as a drug subject to dispensing inspection, an imaging means for imaging the drug assembly placed on the inspection table, and the imaging Based on the imaging information of the means, the medicine name discriminating means for discriminating the drug name of the medicine assembly placed on the examination table, and the weighing for weighing the weight of the medicine assembly placed on the examination table Means and said prescription information Based on the prescription information input by the force means, the number-of-packaging unit-weight relation information stored in the storage means, the medicine name discrimination result by the medicine name discrimination means, and the weighing data of the weighing means Dispensing propriety determining means for determining the propriety of dispensing contents including the drug name of the assembly and the quantity of the drug, and a determination result output means for outputting a determination result by the dispensing propriety determining means, are provided,
The first characteristic configuration is configured such that, when a plurality of types of drug assemblies are placed on the examination table, the drug name determination unit can determine the drug names for each of the plurality of types of drug assemblies,
The dispensing suitability determining means is
If the prescription information includes the names of a plurality of types of prescription drugs, the weight in the number of packaging units corresponding to the prescription quantity in the plurality of types of prescription drugs based on the information on the number of packaging units versus weight and the prescription information The total weight of the prescription drugs, and a total weight tolerance range for determining the propriety of dispensing based on the total weight of the prescription drugs, and the total of a plurality of types of drug aggregates weighed by the weighing means The total weight of the drug assembly, which is the weight, is within the total weight allowable range, and the plurality of drug names determined by the drug name determining means match the names of a plurality of types of prescription drugs included in the prescription information Then, it is configured to output information indicating that the dispensing content is appropriate to the determination result output unit ,
A mode command section for instructing execution of an individual drug name discrimination mode for lifting a kind of drug aggregate from a plurality of kinds of drug aggregates placed on the examination table and discriminating the drug name of the lifted drug aggregate Is provided,
The dispensing suitability determining means is
When the individual medicine name discrimination mode is commanded by the mode command section and the weighing data of the weighing means is reduced, the individual medicine name discrimination mode is executed,
In the individual drug name discrimination mode, the prescription by drug, which is the weight in the number of packaging units corresponding to the prescription quantity of the medicine, for each of a plurality of types of prescription medicines based on the information on the number of packaging units versus weight and the prescription information In addition to obtaining the weight, a drug-specific weight tolerance range for determining the suitability of dispensing is set based on the drug-specific prescription weight, and a decrease value of the weighing data of the weighing means is raised as a drug weight, and each of a plurality of types of prescription drugs It is determined whether or not there is any drug weight tolerance range set for the drug whose lifting drug weight falls within the tolerance range. If there is, the drug name corresponding to the drug weight tolerance range is determined as described above. and outputs the result output means, if not, that lifted drug aggregates are constituted of information indicating that the improperly formulated drug to output the determination result output unit A.

That is, when the dispensing operator places a plurality of types of drug aggregates on the examination table, the imaging means images the plurality of types of drug aggregates placed on the examination table, and based on the imaging information, The drug name discriminating means discriminates the drug name for each of a plurality of types of drug aggregates placed on the examination table, and the weighing means measures the total weight of the drug aggregate, which is the total weight of the plurality of types of drug aggregates. Is weighed.
Then, based on the packaging unit number-to-weight relationship information and the prescription information, the dispensing propriety determination means obtains the total prescription drug weight that is the sum of the weights in the number of packaging units corresponding to the prescription quantities in the plural types of prescription drugs. In addition, a total weight allowable range for determining the propriety of dispensing is set based on the total prescription drug weight, the total weight of the drug assembly measured by the weighing means is within the total weight allowable range, and the drug name is determined. If the names of the plurality of medicines determined by the means match the names of a plurality of kinds of prescription medicines included in the prescription information, the content of the dispensing is determined to be appropriate, and information indicating the determination result is output to the determination result output means Is done.

That is, when multiple types of drugs are prescribed, the dispensing operator collects multiple types of drug aggregates corresponding to the multiple types of prescription drugs, and uses the multiple types of drug aggregates at a time as an examination table. Place. Then, it is determined at once whether or not the dispensing contents of the plurality of types of drug assemblies are appropriate, and information indicating the determination result is output to the determination result output means. This eliminates the need for complicated operations such as determining the suitability of the contents of dispensing, and simplifies and shortens the dispensing auditing work.
Accordingly, it has become possible to provide a dispensing inspection system that can improve the efficiency of dispensing inspection work.

Further , when the dispensing operator lifts a predetermined type of drug assembly from a plurality of types of drug assemblies placed on the examination table and instructs the individual drug name determination mode by the mode command unit, the individual drug name The discrimination mode is executed.
In the individual drug name discrimination mode, a prescription weight for each drug is obtained for each of a plurality of types of prescription drugs based on the number of packaging units vs. weight relationship information and prescription information, and the dispensing suitability determination is based on the prescription weight for each drug. The drug-specific weight tolerance is set.
Subsequently, the reduced value of the weighing data of the weighing means is set as the lifted drug weight, and whether there is a lifted drug weight that falls within the allowable range among the drug-specific weight allowable ranges set for each of the plural types of prescription drugs. If yes, the drug name corresponding to the weight tolerance range for each drug is output to the determination result output means. If not, the lifted drug assembly is an improperly dispensed drug. Is output to the determination result output means.

Then, when the drug name is output to the determination result output unit, the dispensing operator visually recognizes the drug name of the lifted drug assembly, and the recognized drug name is output to the determination result output unit. If it matches the name, it can be seen that the dispensing content for the lifted drug assembly is appropriate, and if it does not match, the dispensing content for the lifted drug assembly is incorrect. In addition, when information indicating that the lifted drug assembly is a drug that has been improperly dispensed is output to the determination result output means, it is understood that the content of the dispensed drug aggregate is inappropriate. .
In other words, for each of a plurality of types of drug assemblies placed on the examination table, when the individual drug name determination mode is executed in order by lifting and returning one by one, which drug among the plurality of types of drug assemblies is selected. Since it can be seen whether the dispensing content of the assembly is inappropriate, it is possible to quickly and accurately find a drug assembly whose dispensing content does not match the prescription information.
Therefore, the efficiency of the dispensing inspection work can be further increased.

The dispensing inspection system according to the present invention provides the number of packaging units versus weight relationship information indicating the relationship between the number of packaging units and the weight, which is the number of medicines in the packaging unit in a state of being packaged with a packaging material. Based on the prescription information, storage means for storing the medicine code corresponding to each medicine name in association with each other, prescription information input means for inputting prescription information including the name and prescription quantity of the prescribed prescription medicine An inspection table on which a drug assembly in which the drugs are collected while being packaged in a packaging material is placed as a drug subject to dispensing inspection, an imaging means for imaging the drug assembly placed on the inspection table, and the imaging Based on the imaging information of the means, the medicine name discriminating means for discriminating the drug name of the medicine assembly placed on the examination table, and the weighing for weighing the weight of the medicine assembly placed on the examination table Means and said prescription information Based on the prescription information input by the force means, the number-of-packaging unit-weight relation information stored in the storage means, the medicine name discrimination result by the medicine name discrimination means, and the weighing data of the weighing means Dispensing propriety determining means for determining the propriety of dispensing contents including the drug name of the assembly and the quantity of the drug, and a determination result output means for outputting a determination result by the dispensing propriety determining means, are provided,
The second feature configuration is configured such that, when a plurality of types of drug assemblies are placed on the examination table, the drug name determination unit is capable of determining a drug name for each of a plurality of types of drug assemblies,
The dispensing suitability determining means is
If the prescription information includes the names of a plurality of types of prescription drugs, the weight in the number of packaging units corresponding to the prescription quantity in the plurality of types of prescription drugs based on the information on the number of packaging units versus weight and the prescription information The total weight of the prescription drugs, and a total weight tolerance range for determining the propriety of dispensing based on the total weight of the prescription drugs, and the total of a plurality of types of drug aggregates weighed by the weighing means The total weight of the drug assembly, which is the weight, is within the total weight allowable range, and the plurality of drug names determined by the drug name determining means match the names of a plurality of types of prescription drugs included in the prescription information Then, it is configured to output information indicating that the dispensing content is appropriate to the determination result output unit,
The examination table is divided into a plurality of placement sections that can be placed by dividing a plurality of types of drug aggregates by type,
The weighing means is provided corresponding to each placement section, and includes a plurality of section weighing sections capable of weighing the weight of the drug assembly placed in each placement section,
The drug name determination means is configured to determine the drug name of each of a plurality of types of drug assemblies placed on the examination table in association with each of the plurality of placement sections,
The dispensing suitability determining means is
The total of the weighing results of the plurality of compartment weighing units is used as the total weight of the drug assembly, and is configured to determine the suitability of the contents of dispensing, and
When the total weight of the drug assembly is not within the total weight allowable range, the packaging unit corresponding to the prescription quantity of the drug for each of a plurality of types of prescription drugs based on the information on the number of packaging units versus the weight and the prescription information The prescription weight for each medicine, which is a weight in number, is determined, and the weight tolerance for each medicine for determining the suitability of dispensing is set based on the prescription weight for each medicine. The weight of the drug assembly weighed in the section weighing section of the section is determined to be not within the weight tolerance range for each drug corresponding to the drug name determined corresponding to the placement section, and the determination result is determined. It is the point which is comprised so that it may output to the said determination result output means.

That is, when the dispensing operator places a plurality of types of drug aggregates on the examination table, the imaging means images the plurality of types of drug aggregates placed on the examination table, and based on the imaging information, The drug name discriminating means discriminates the drug name for each of a plurality of types of drug aggregates placed on the examination table, and the weighing means measures the total weight of the drug aggregate, which is the total weight of the plurality of types of drug aggregates. Is weighed.
Then, based on the packaging unit number-to-weight relationship information and the prescription information, the dispensing propriety determination means obtains the total prescription drug weight that is the sum of the weights in the number of packaging units corresponding to the prescription quantities in the plural types of prescription drugs. In addition, a total weight allowable range for determining the propriety of dispensing is set based on the total prescription drug weight, the total weight of the drug assembly measured by the weighing means is within the total weight allowable range, and the drug name is determined. If the names of the plurality of medicines determined by the means match the names of a plurality of kinds of prescription medicines included in the prescription information, the content of the dispensing is determined to be appropriate, and information indicating the determination result is output to the determination result output means Is done.
That is, when multiple types of drugs are prescribed, the dispensing operator collects multiple types of drug aggregates corresponding to the multiple types of prescription drugs, and uses the multiple types of drug aggregates at a time as an examination table. Place. Then, it is determined at once whether or not the dispensing contents of the plurality of types of drug assemblies are appropriate, and information indicating the determination result is output to the determination result output means. This eliminates the need for complicated operations such as determining the suitability of the contents of dispensing, and simplifies and shortens the dispensing auditing work.
Accordingly, it has become possible to provide a dispensing inspection system that can improve the efficiency of dispensing inspection work.
Further , a plurality of types of drug aggregates are classified according to type and placed on a plurality of placement sections.
Then, the drug names of the plurality of types of drug assemblies placed on the examination table are determined in correspondence with the plurality of placement sections, and the weight of the drug assembly in each placement section is determined for each placement section. Are weighed in a section weighing section corresponding to
The total weight of the drug assembly, which is the sum of the weighing results of each section weighing unit, is within the total weight allowable range, and a plurality of types in which a plurality of drug names determined by the drug name determination unit are included in the prescription information If it matches the name of the prescription drug, information indicating that the content of the dispensing is appropriate is output to the determination result output means.
In addition, when the total weight of the drug assembly is not within the total weight allowable range, the prescription weight for each prescription drug is obtained for each of a plurality of prescription drugs based on the number of packaging units versus the weight relation information and the prescription information. Based on the prescription weight, an acceptable weight range for each drug for determining the suitability of dispensing is set, and among the plurality of placement sections, the weight of the drug assembly measured by the section weighing section of each placement section Those that are not within the permissible drug weight corresponding to the medicine name determined corresponding to the placement section are determined, and the determination result is output to the determination result output means.

In other words, when a plurality of types of drug assemblies are placed on the examination table all at once, it is not only determined whether or not the contents of the plurality of types of drug assemblies are appropriate. Since it can be determined whether the dispensing content of the medicine assembly in the placement section is not appropriate, when the dispensing content does not match the prescription information, a drug that does not match the prescription information can be found quickly and accurately.
Therefore, the efficiency of the dispensing inspection work can be further increased.

The third feature configuration is in addition to the second feature configuration,
Each of the plurality of placement sections is configured to include a base portion that protrudes upward from the peripheral portion of each placement section,
Each compartment weighing unit is configured to weigh the load applied to each platform,
An inspection tray that can be placed on the examination table and includes a plurality of storage compartments corresponding to the plurality of placement compartments that can contain a plurality of types of drug aggregates by type, and is provided.
The inspection tray forms a tray main body having a frame section for dividing and forming the plurality of storage sections, and forms a bottom portion of each storage section, and is relatively movable in the vertical direction with respect to the frame section in each storage section. Each of the receiving sections is provided with a mounting plate, and each mounting plate is lifted by each base portion as the tray body is mounted on the inspection table. It is in the point comprised so that it may be mounted and supported by a part.

That is, a plurality of types of drug assemblies are classified according to type and stored in a plurality of storage sections of the inspection tray, and the inspection tray is placed on the inspection table.
Then, the mounting plate of each receiving section of the inspection tray is lifted by each base portion of the inspection table and is placed and supported on each base portion, and is placed on the mounting plate and the mounting plate. Since the load of the drug assembly is applied to the platform, the weight of the drug assembly placed in each placement section can be weighed by each section weighing unit.
That is, a plurality of types of drug aggregates collected based on prescription information are classified according to type and stored in a plurality of storage compartments of a dispensing tray, and when the dispensing tray is placed on an examination table as it is, When the determination of dispensing contents is performed all at once, and the determination is inappropriate, it is possible to identify a drug assembly with an inappropriate dispensing content as it is (without having to lift and return one by one). Done.
Therefore, the efficiency of the dispensing inspection work can be further increased.

The fourth feature configuration is in addition to any one of the first to third feature configurations,
Image display means for displaying an image picked up by the image pickup means is provided;
When there is a drug assembly whose drug name cannot be identified among a plurality of types of drug assemblies placed on the examination table, the drug name determination unit displays the drug name on the image display unit. It is configured to display information indicating that the drug name cannot be identified in association with the image of the drug aggregate that cannot be identified.

That is, when a plurality of types of drug aggregates are placed on the examination table and there are drug aggregates whose drug names cannot be identified among the plurality of types of drug aggregates, the drug name is displayed on the image display means. The information indicating that the drug name cannot be determined is displayed in association with the image of the drug assembly that cannot be determined. Therefore, based on the display content, the drug assembly whose drug name cannot be determined is a plurality of types of drug assemblies. You can see which one is.
Therefore, based on the display content of the image display means, the dispensing operator changes the posture on the examination table of the drug assembly whose drug name could not be determined by changing the orientation or turning it over, The drug name can be determined again. As a result, even if there is a drug assembly for which the drug name cannot be identified among a plurality of types of drug assemblies, the drug names of all the drug assemblies can be identified as quickly as possible, and the suitability of the dispensing contents can be determined. Can be done.
Therefore, the efficiency of the dispensing inspection work can be further increased.

In addition to any one of the first to fourth feature configurations described above, the fifth feature configuration is
When the prescription quantity included in the prescription information is equal to or greater than the set prescription quantity for adding the rubber band weight, the prescription quantity of the drug for each of a plurality of types of prescription drugs under the condition for adding the set rubber band weight The prescription weight classified by medicine which is the weight in the number of packaging units corresponding to is obtained, and the total weight of the prescription medicine is obtained based on the obtained prescription weight by medicine.

  That is, when the prescription quantity included in the prescription information is equal to or greater than the set prescription quantity for adding the rubber band weight, the prescription weight for each drug is obtained for each of the plural types of prescription drugs under the condition of adding the set rubber band weight. The total prescription drug weight is determined based on the prescription weight for each drug. Based on the total prescription drug weight thus determined, the suitability of the content of the dispensing is determined.

In other words, a collective package in which a predetermined number of packaging units (dome-shaped or bag-shaped accommodating portions) containing medicines are usually formed by a packaging material such as a PTP sheet. If the prescription quantity included in the prescription information is greater than the number of packaging units that make up the collective package, combine the package assembly or a fraction package assembly that is obtained by separating an unnecessary number of packaging units from the package assembly. Collect as a drug assembly. When the collected drug assembly is composed of a plurality of collective package bodies or a combination of the collective package bodies and the fraction collective package bodies, they are bundled together with rubber bands.
Then, when it is predicted that the rubber band is used by setting the set prescription quantity for adding the rubber band weight to the number of the packaging units constituting the collective package, the weight of the rubber band is taken into consideration in preparation. Since it is possible to appropriately determine the suitability of the quantity of the medicines that have been dispensed, a dispensing audit can be performed appropriately.

The sixth feature configuration is in addition to any one of the first to fifth feature configurations,
From the imaging information of the imaging means, the medicine name discriminating means displays the medicine name displayed on the medicine and the medicine code corresponding to the medicine name, and the medicine name and medicine name displayed on the packaging material packaging the medicine. The medicine code is identified by identifying one of the medicine codes corresponding to the medicine name.

That is, a medicine name and a medicine code corresponding to the medicine name are displayed on the packaging material in which the medicine is packaged by printing or the like. In addition, the medicine name and medicine code may be displayed on the medicine by printing or engraving.
And any one of the medicine name and the medicine code displayed on the medicine and the medicine name and the medicine code displayed on the packaging material packaging the medicine from the imaging information of the imaging means by the medicine name discrimination means Is identified, and the drug name is determined.
That is, for example, when it is difficult to identify one drug name displayed on the packaging material, it becomes possible to identify the drug name by identifying other drug names and drug codes displayed on the packaging material, The ability to discriminate drug names can be further improved.
Therefore, the efficiency of the dispensing inspection work can be further increased.

The block diagram which shows the whole structure of the dispensing inspection system which concerns on 1st Embodiment. The perspective view which shows the external appearance in the state which pulled out the drawer part in the dispensing inspection unit which concerns on 1st Embodiment. The perspective view which shows the external appearance in the state which accommodated the drawer part in the dispensing inspection unit which concerns on 1st Embodiment. Longitudinal front view of the dispensing inspection unit according to the first embodiment Diagram showing the collective package of drugs Diagram showing the collective package of drugs Diagram showing the collective package of drugs The perspective view which shows the dispensing tray which accommodated the multiple types of chemical | medical agent assembly which concerns on 1st Embodiment. The figure which shows the initial screen of the display apparatus which concerns on 1st Embodiment. The figure which shows the audit exclusion chemical | medical agent setting screen of the display apparatus which concerns on 1st Embodiment. The figure which shows the chemical | medical agent name rejection determination screen of the display apparatus which concerns on 1st Embodiment. The figure which shows the flowchart of control operation of the dispensing inspection system which concerns on 1st Embodiment. The block diagram which shows the whole structure of the dispensing inspection system which concerns on 2nd Embodiment. The perspective view which shows the external appearance in the state which pulled out the drawer part in the dispensing inspection unit which concerns on 2nd Embodiment. The perspective view which shows the inspection table and weighing device which concern on 2nd Embodiment. The perspective view of the dispensing tray which concerns on 2nd Embodiment. Longitudinal side view of a dispensing tray according to the second embodiment Longitudinal side view of the inspection table and weighing device in a state where the dispensing tray according to the second embodiment is placed. The figure which shows the flowchart of control operation of the dispensing inspection system which concerns on 2nd Embodiment.

Hereinafter, embodiments of the present invention will be described with reference to the drawings.
[First Embodiment]
First, a first embodiment will be described based on the drawings.
As shown in FIG. 1, the dispensing audit system includes a central control device C that executes control of each device constituting the dispensing audit system and various processes in dispensing audit, a storage device 11 that stores various information, and various information. An input device 12 for inputting, a display device 13 for displaying and outputting various information, a printing device 14 for printing and outputting various information, and a medicine 2 (see FIGS. 5 to 7) based on prescription information described in a prescription 3 (see FIG. 5 to FIG. 7) is placed on the examination table 15 (see FIG. 2) on which the medicine assembly 1 collected in a packaged state is placed as a medicine subject to dispensing inspection. The imaging device 16 as an imaging means for imaging the medicine assembly 1, the weighing device 17 as a weighing means for weighing the weight of the medicine assembly 1 placed on the examination table 15, and the dispensing inspection system are operated. Power for It is configured to include a supply power supply 18 and the like.

In this embodiment, the storage device 11 is configured by an HDD built in the central control device C. The storage device 11 is not limited to the one built in the central controller C, and may be an external device.
In this storage device 11, the packaging unit number-to-weight relationship information indicating the relationship between the number of packaging units and the weight, which is the number of medicines 2 in the packaging unit packaged in the packaging material 3, includes a plurality of medicines The name is stored in association with each name, and the storage device 11 corresponds to a storage unit.

  In this embodiment, the input device 12 is configured by an OCR (Optical Character Reader). When a prescription created by a doctor is set at a predetermined position, the input device 12 includes a prescription drug name and a prescription quantity described in the prescription. Information can be read and functions as a prescription information input means.

  The central controller C is configured with a microcomputer, and a program for executing various processes is installed. The program includes a drug name determination unit P1 for executing a drug name determination process for determining the name of the drug assembly 1 placed on the examination table 15 based on the imaging information of the imaging device 16, and an input device. 12, based on the prescription information input in 12, the number-of-packaging unit-weight relationship information stored in the storage device 11, the drug name discrimination result by the drug name discrimination means P 1, and the weighing data of the weighing device 17. Dispensing suitability determination means P2 for executing a dispensing auditing process for determining the suitability of the contents of the dispensing including the name and quantity of the body 1 is included.

Although illustration is omitted, when this dispensing inspection system is installed in a hospital, the central controller C is connected to a hospital host computer via a LAN, and this dispensing audit system is installed in a dispensing pharmacy. In this case, the central controller C is connected to the host computer of the management department that supervises the dispensing pharmacy via the Internet.
And the program memorize | stored in the memory | storage device 11 and memorize | stored information, such as packaging unit number versus weight relationship information, are comprised so that it can update by a host computer.

  In this embodiment, the display device 13 is configured by an LCD, and a touch panel type operation unit 19 for inputting various commands to the central control device C is provided on the display surface.

  As shown in FIG. 1 to FIG. 4, among the devices constituting the dispensing inspection system, the central control device C, the display device 13, the touch panel type operation unit 19, the inspection table 15, the imaging device 16, which incorporates the storage device 11. The weighing device 17 and the power supply device 18 are integrally assembled using a casing 20 and configured in the dispensing inspection unit U.

Next, the dispensing auditing unit U will be described based on FIGS.
The casing 20 is configured in a substantially rectangular parallelepiped box shape in which the outer shape in a plan view is a rectangular shape, and the upper part of the front surface is an obliquely upward inclined portion.
In the dispensing inspection unit U, the drawer 21 is housed in an imaging space 23 (details will be described later) formed in the casing 20 through a drawer opening 22 provided at the lower end of the front surface of the casing 20. It is provided in such a manner that it can be retracted and retracted at a storage position where it is pulled out and a drawing position where it is pulled out forward of the casing 20.
Further, the drawer portion 21 is provided with a lid 24 so as to close the drawer opening 22 of the casing 20 when the drawer portion 21 is located at the storage position.
The drawer portion 21 is supported on the casing 20 by a pair of slide rails 25 that are arranged in a left and right manner so as to be slidable in the horizontal direction between the storage position and the drawer position.

The inspection table 15 is provided on the upper portion of the drawing portion 21 and can place a dispensing tray 26 for storing the drug assembly 1 collected by a dispensing operator (pharmacist or the like).
Further, although the illustration of the installation state is omitted, a load detection sensor (for example, a load cell) constituting the weighing device 17 is arranged so that the load of the inspection table 15 is applied, and the weighing device 17 detects the load detection sensor. Based on the signal, the load applied to the examination table 15 is weighed. Incidentally, the weighing accuracy of the weighing device 17 is, for example, 10 mg.
In order to conduct a dispensing audit of the dispensed medicine, the dispensing tray 26 containing the collected medicine assembly 1 is placed on the inspection table 15, but the weighing device 17 is not shown in the figure. A function of canceling the tare of the dispensing tray 26 and the like that has been measured and stored in advance is provided. By canceling the tare, the collected medicine assembly 1 is stored in the dispensing tray 26 in the inspection table 15. Even when placed, the weight of the drug assembly 1 can be weighed.

  As shown in FIG. 4, a substantially dome-shaped reflector 27 is disposed in the casing 20 so as to cover the upper part of the drawer portion 21 located at the storage position, and the imaging space 23 is provided inside the reflector 27. Is formed. In the casing 20, the central control device C and the power supply device 18 are disposed at the rear of the reflector 27.

At the top of the dome-shaped reflector 27, the imaging device 16 is disposed so that the entire dispensing tray 26 placed on the examination table 15 can be imaged from above, and a pair of reflectors 27 is disposed below the reflector 27. The lighting devices 28 are arranged separately on the left and right sides. Incidentally, the imaging device 16 is configured using an electronic imaging device such as a CCD device or a CMOS device. Moreover, each illuminating device 28 is comprised with the fluorescent lamp, for example.
As shown in FIGS. 2 and 3, the display device 13 in which the touch panel type operation unit 19 is incorporated in the display surface is disposed in an obliquely upward inclined portion at the upper front of the casing 20.

As shown in FIG. 2, when the dispensing tray 26 storing the drug assembly 1 is placed on the inspection table 15 and the drawer portion 21 is pushed into the casing 20 to the storage position, as shown in FIG. Since the 20 extraction openings 22 are closed by the lid 24 of the extraction portion 21, it is possible to prevent external light from entering the imaging space 23 and light from the illumination device 28 from leaking to the outside.
The medicine assembly 1 in the dispensing tray 26 placed on the examination table 15 is imaged by the imaging device 16 in a state where the imaging space 23 is illuminated by the pair of lighting devices 28.

Next, a description will be given of the number-of-packaging unit-weight relationship information stored in the storage device 11.
Even if the components contained in the drug 2 are the same, there are some types of drugs 2 of the same component due to the different contents. Therefore, when there are a plurality of types having the same components but different contents, the name of the drug 2 is, for example, “Al XX tablet 10 mg”, “Al XX tablet 20 mg” The name also includes the content of. Incidentally, the name of the medicine 2 having only one kind of content is, of course, a name that does not include the content of the component, such as “GLOOO”.

Examples of the form of the medicine 2 include a tablet shape, a capsule shape, a granule shape, and a fine particle shape.
As shown in FIGS. 5 to 7, the packaging material 3 for packaging the drug 2 includes a sheet-shaped packaging material 3 s such as a PTP sheet for packaging a plurality of tablets and capsules, and a granular or fine powder powder. There is a seal wrapping material 3t for packaging.
As shown in FIGS. 5 and 6, a plurality of dome-shaped packaging bodies 4 (corresponding to packaging units) that individually accommodate tablets and capsules one by one are arranged in a lattice pattern by the sheet-shaped packaging material 3 s. A sheet-like collective package 5 is formed. As shown in FIG. 7, a band-shaped collective package 5 in which a plurality of bag-shaped packages 4 (corresponding to a packaging unit) are continuous in a band shape is formed by the seal packaging material 3t. Each bag-like package 4 contains a predetermined amount of granules or fine powder.
In the following description, when the names of the medicines 2 are distinguished from each other, the signs “a”, “b”, “c”,... A description will be given.

As shown in FIG. 5, in the tablet A medicine 2a, ten dome-shaped packaging bodies 4 are combined into one in a sheet-shaped packaging material 3s to form a sheet-shaped collective packaging body 5. As shown in FIG. 6, the capsule B medicine 2 b is also formed by combining the 10 packaging bodies 4 into one in the sheet-shaped packaging material 3 s to form the sheet-shaped collective packaging body 5. On the other hand, as shown in FIG. 7, in the powder C medicine 2c, ten bag-shaped packaging bodies 4 are combined into one in the sealing packaging material 3t to form a strip-shaped collective packaging body 5.
The number of the packaging bodies 4 forming the collective packaging body 5 is not limited to the above-described 10 pieces, but is convenient when set to 20 pieces or 30 pieces or for a weekly prescription period. , A multiple of 7 (for example, 14 or 21) may be set.

As shown in FIG. 8, when the prescribed quantity of the prescribed medicine 2 is less than the number of the packaging bodies 4 constituting the collective packaging body 5, the dispensing operator is unnecessary, for example, A medicine 2 a. The fraction set package 5 h from which the package 4 is cut is collected as the drug assembly 1.
Further, when the prescribed quantity of the prescribed medicine 2 is larger than the number of the packaging bodies 4 constituting the assembly packaging body 5, for example, the assembly packaging body 5 and the fractional assembly like the B medicine 2b and the C medicine 2c. The package 5h is combined and collected as the drug assembly 1. And when the medicine assembly 1 of the dispensed medicine 2 is composed of a plurality of assembly packaging bodies 5 or a combination of the assembly packaging body 5 and the fraction assembly packaging body 5h, they are bundled together with a rubber band 6.
In the following, when the drug assembly 1 is described by distinguishing the name of the drug 2, the reference numerals “a”, “b”, “ c ”……………….

The number-of-packaging-units-to-weight relationship information is set by determining the weight in association with the number of packages 4 (corresponding to the number of packaging units) for each drug 2 name.
This weight is set based on the actual measurement data, for example, by actually measuring the weight for each number of the packaging bodies 4 in the state where the medicine 2 is packaged by the packaging material 3 and averaging the actual measurement data.
For example, in the case of the medicine A 2a, when the number of the packaging bodies 4 is 10 which is the same as the number of the packaging bodies 4 constituting the assembly packaging body 5, the actual measurement is performed in the packaging state of the assembly packaging body 5 as shown in FIG. When the number of the packaging bodies 4 is set based on the information thus obtained and is smaller than the number of the packaging bodies 4 constituting the assembly packaging body 5, the fractional assembly packaging body 5h having a shape corresponding to the number of the packaging bodies 4 (for example, If the number of the wrapping bodies 4 is 7, the shape is set based on the information measured in the packaging state according to the shape shown in FIG.

Further, when the number of the wrapping bodies 4 is larger than the number of the wrapping bodies 4 constituting the collective wrapping body 5, the number is set based on information measured by the combination of the collective wrapping body 5 and the fractional collective wrapping body 5h. .
When the number of the wrapping bodies 4 is larger than the number of the wrapping bodies 4 constituting the collective wrapping body 5, the set rubber band weight is added and the weight is determined in association with the number of the wrapping bodies 4. The set rubber band weight is set according to the weight of the rubber band 7 used for bundling the plurality of collective package bodies 5 and the fraction collective package bodies 5h.
For example, in the medicine A 2a, the number of the packaging bodies 4 constituting the collective packaging body 5 is 10, so that when the number of the packaging bodies 4 is 11 or more, the set body rubber weight is added and the packaging body 4 is added. The weight is determined in association with the number of.

Next, a description will be given of the drug name displayed on the packaging material 3 of the drug 2 and the drug code corresponding to the drug name.
As shown in FIGS. 5 to 7, the medicine name and the medicine code are printed on the packaging material 3 of the medicine 2. 5 and 6, (a) shows the surface of the collective package 5, and (b) shows the back surface of the collective package 5. FIG. 7 shows the surface of the collective package 5.
5-7, the code | symbol 7 is the pattern (it may be described as a name pattern hereafter) which printed the medicine name, and the code | symbol 8 is the pattern (henceforth a code pattern) which printed the medicine code. May be). Incidentally, as the medicine code, there are a bar code and the like in addition to a form set by combining a plurality of alphabets, numerals, marks for identifying a pharmaceutical manufacturer, and the like as shown in FIGS.

For example, as shown in FIG. 5, in the A medicine 2a packaged in the sheet-shaped packaging material 3s, the name pattern 7 is printed on the surface of the sheet-shaped packaging material 3s forming the collective package 5, and on the back surface, A name pattern 7 and a code pattern 8 are printed.
In other words, the name pattern 7 is a pattern such as “AlOO tablet 10 mg”, and the code pattern 8 is a pattern such as “AOO”.
As shown in FIG. 6, the name pattern 7 is printed on the surface of the sheet-shaped packaging material 3s forming the collective package 5 in the B drug 2b packaged in the sheet-shaped packaging material 3s as in the case of the drug A 2a. The name pattern 7 and the code pattern 8 are printed on the back surface.
That is, the name pattern 7 is “Serve XX50 mg”, “Sel XX × 50 mg”, and the code pattern 8 is “S50 OO”.
As shown in FIG. 7, in the C medicine 2c packaged in the seal package 3t, a name pattern 7 such as “Show XXX” is printed on the surface of the seal package 3t forming the assembly package 5. Has been.

Next, description is added about prescription information described in the prescription.
The prescription information includes information for identifying the patient such as the patient name, and the number of times of medication taken per day, the time taken, and the number of medication taken per time (for example, the number of tablets, the number of capsules, etc.) , Number of bags), number of days taken, etc. Here, the product of the quantity taken per day and the number of days taken is the prescription quantity.
For example, A drug 2a is described as “Al XX tablet 10 mg once a day: 1 tablet after dinner for 7 days”, and B drug 2b is “Selve XX 50 mg twice a day: morning”・ It is described as “1 tablet 7 days after dinner”, and C drug 2c is described as “show XX 2 times a day: each morning 7 days after dinner 7 bags each”.
That is, the prescription quantity is 7 for the A medicine 2a, and the prescription quantity is 14 for the B medicine 2b and the C medicine 2c.

  When a prescription (not shown) is set in the input device 12, the above prescription information described in the prescription is read and input to the central controller C. For example, when there are a plurality of types of prescription drugs, the names of a plurality of types of prescription drugs and the prescription quantities corresponding to the names of the plurality of types of prescription drugs are input.

Based on the prescription information described in the prescription, the dispensing operator collects the prescription quantity of the medicine 2 as the medicine assembly 1 in a state of being packaged in the packaging material 3. When the names of a plurality of types of prescription drugs are described in the prescription, a plurality of types of drug assemblies 1 are collected corresponding to the plurality of types of prescription drugs.
For example, when the names of three types of prescription drugs, A drug 2a, B drug 2b, and C drug 2c, are described in the prescription, the prescription quantity for A drug 2a is 7, so that it is shown in FIG. In this way, the fraction set package 5h for seven packages separated from the three packages is collected as the drug assembly 1a. Since the prescription quantity for B medicine 2b is 14, as shown in FIG. 8, one collective package 5 and fraction collective package 5h for four packages are collected as drug aggregate 1a. The collective package 5 and the fraction collective package 5h are bundled together with a rubber band 6 one by one.
Since the prescription quantity for C medicine 2c is 14, as well as B medicine 2b, as shown in FIG. 8, one set package 5 and one fraction set 5h are grouped together with rubber band 6. Bundle it up.

Next, the control operation of the central controller C will be described.
In the present invention, when a plurality of types of drug assemblies 1 are placed on the examination table 15, the drug name determination unit P <b> 1 is configured to be able to determine the drug names for each of the plurality of types of drug assemblies 1.
When the dispensing propriety determining means P2 includes the names of a plurality of types of prescription drugs in the prescription information, the dispensing audit process determines the number of prescription drugs in the plurality of types of prescription drugs based on the number of packaging units versus the weight relationship information and the prescription information. The total weight of the prescription drug, which is the sum of the weights in the number of packaging units corresponding to the prescription quantity, is obtained, and a total weight allowable range for determining the suitability of dispensing is set based on the total prescription drug weight. The total weight of the drug assembly, which is the total weight of the weighed plural kinds of drug assemblies 1, is within the total weight tolerance, and the plurality of drug names determined by the drug name determining means P1 are included in the prescription information. When it matches the names of a plurality of types of prescription drugs, information indicating that the content of dispensing is appropriate is displayed and output on the display device 13 (corresponding to the determination result output means).

Hereinafter, explanation will be given on the medicine name discrimination processing by the medicine name discrimination means P1 and the dispensing inspection processing by the dispensing suitability judgment means P2.
First, the drug name determination process by the drug name determination unit P1 will be described. Since the drug name determination unit P1 is configured using a known image recognition program, a detailed algorithm of the drug name determination process will be described. Omitted, the basic functions are briefly described.
In the storage device 11, a reference pattern (hereinafter referred to as a reference name pattern) corresponding to the name pattern 7 printed on the packaging material 3 for packaging the medicine 2 and a reference pattern (hereinafter referred to as a reference) corresponding to the code pattern 8. Reference pattern information consisting of a code pattern) is stored in association with each of a plurality of drug names.
When the name of the medicine 2 is printed in a plurality of name patterns 7 having different forms on the packaging material 3 for packaging the medicine 2, the reference pattern information includes a plurality of names having different forms for the medicine 2. A plurality of reference name patterns corresponding to the pattern 7 are stored. Similarly, when the medicine code of the medicine 2 is printed on the packaging material 3 for packaging the medicine 2 with a plurality of code patterns 8 having different forms, the reference pattern information includes the form for the medicine 2. A plurality of reference code patterns corresponding to a plurality of different code patterns 8 are stored.

  For example, for the A medicine 2a, a reference name pattern such as “Al XX tablet 10 mg” indicated by reference numeral 7 in FIG. 5 is stored, and a reference code pattern is indicated by reference numeral 8 in FIG. A pattern such as “A ○ 1 ○” is stored. For the B medicine 2b, patterns such as “Selve XX50 mg” and “Sel XXx50 mg” indicated by reference numeral 7 in FIG. 6 are stored as the reference name pattern, and the reference code pattern is shown in FIG. In FIG. 8, a pattern such as “S 50” indicated by reference numeral 8 is stored.

The medicine name discriminating means P1 identifies the image of the drug assembly 1 from the captured image of the imaging device 16, and identifies the name pattern 7 and the code pattern 8 from the image information of the medicine assembly 1, and identifies them. The name pattern 7 and the code pattern 8 are sequentially compared with the reference name pattern and the reference code pattern of the reference pattern information of the storage device 11, and the name of the medicine 2 corresponding to the reference name pattern and the reference code pattern having the highest degree of matching is obtained. It is determined as the drug name of the assembly 1.
In addition, when a plurality of patterns such as the name pattern 7 and the code pattern 8 are identified from the image information of the drug assembly 1, if the drug name cannot be determined due to the low matching level, the matching level of the next pattern Are compared with the reference pattern information in the storage device 11 one by one in order, and the drug name of the drug assembly 1 is determined.
That is, the medicine name discrimination means P1 identifies either the medicine name displayed on the packaging material 3 in which the medicine 2 is packaged or the medicine code corresponding to the medicine name from the imaging information of the imaging device 16. This means that the medicine name is determined.

  When identifying a plurality of types of drug assemblies 1 from the captured image of the imaging device 16, the drug name determination unit P1 executes a drug name determination process as described above for each of the plurality of types of drug assemblies 1, The drug names are determined for all of the multiple types of drug assemblies 1.

When the drug name discriminating means P1 identifies a plurality of types of drug aggregates 1 from the captured image of the imaging device 16 and cannot identify the drug names of all the drug aggregates 1, the drug name discriminating means P1 11 displays a “drug name rejection screen”. In this “drug name rejection determination screen”, an image captured by the imaging device 16 is displayed, and an image of the drug assembly 1 whose drug name could not be determined is surrounded by a frame or the like. In addition to the image, information indicating that the drug name cannot be determined, such as “cannot be determined”, is displayed in association with the image of the drug assembly 1 whose drug name could not be determined.
Incidentally, the “drug name rejection screen” shown in FIG. 11 illustrates the case where the drug name of the leftmost drug assembly 1 (the drug assembly 1a of the drug A 2a) cannot be determined. In addition, 19f in FIG. 11 is a “screen switching” button. When this “screen switching” button 19f is touched, an initial screen (details will be described later) shown in FIG. .

That is, the display device 13 is configured to display an image picked up by the image pickup device 16 (corresponding to an image display means).
Then, when there is a drug assembly 1 in which the drug name cannot be determined among the plurality of types of drug assemblies 1 placed on the examination table 15, the drug name determination unit P1 The information indicating that the drug name cannot be identified is displayed in association with the image of the drug assembly 1 in which the drug name cannot be identified.

Next, the dispensing audit process by the dispensing suitability determination unit P2 will be described.
When the dispensing audit system is activated, an initial screen is displayed on the display device 13 as shown in FIG. 9, and in the initial screen, a “dispensing audit” button 19 a constituting the touch panel type operation unit 19, “excluded medicine for auditing” is displayed. A “set” button 19b, an “individual drug name discrimination mode” button 19c, a “prescription information import” button 19d, and an “end” button 19e are displayed.
When the “END” button 19e is touched, the dispensing inspection system is stopped. The functions of the buttons other than the “end” button 19e will be described in detail below.

When the “prescription information import” button 19d is touched, the prescription information described in the prescription is read by the input device 12, and the read prescription information is taken into the central controller C.
When a plurality of types of prescription drugs are described in the prescription, the name and the prescription quantity corresponding to the name of each prescription drug are captured for all of the plurality of types of prescription drugs.

As shown in FIG. 10, an “audit excluded medicine setting” button 19b is touched, and an audit excluded medicine setting screen is displayed.
In the audit exclusion medicine setting screen shown in FIG. 10, buttons corresponding to the names of all the prescription medicines in the prescription information input by the input device 12 are displayed. For example, the name of the prescription drug in the prescription information is “Al XX tablet 10 mg” which is the drug name of A drug 2a, “Selve XX 50 mg” which is the drug name of B drug 2b, and the drug of C drug 2c In the case of the name “Show XXX” and the name of the D medicine 2d “Sari XX ointment”, four “medicine name” buttons 19g corresponding to each medicine name. To 19j and a “screen switching” button 19f.

Then, when any one of the plurality of “medicine name” buttons 19g to 19j displayed on the audit exclusion medicine setting screen is touched, the medicine name corresponding to the touched “medicine name” button 19g to 19j is changed from the dispensing audit target. Excluded. For example, when the “sari ○○○○ ointment” button 19j is touched, the D medicine 2d having the medicine name “SariOOOO ointment” is excluded from the dispensing audit target.
Accordingly, it is possible to exclude drugs that do not necessarily need to be audited for dispensing, drugs that are packed in bottle-shaped containers, etc., and whose drug names are difficult to distinguish, from the targets for auditing.

When the “Dispensing Audit” button 19a is touched, the dispensing propriety determination means P2 first sets the name of the prescription drug subject to the dispensing audit, and based on the prescription information about the set prescription drug targeted for the dispensing audit, Started dispensing audit process.
In other words, when no medicine name to be excluded from the dispensing audit is set on the audit exclusion medicine setting screen, all of the names of the plurality of prescription drugs taken in are set as dispensing audit targets. On the other hand, when a drug name to be excluded from the dispensing audit is set on the audit excluded drug setting screen, the dispensing suitability determining means P2 displays the audit excluded drug setting screen among the names of the plurality of types of prescription drugs taken in. The name of the prescription drug excluding the set drug name is set as the dispensing audit target.

  For example, if the names of the prescription drugs taken in are “Al XX Tablets 10 mg”, “Selbe XX 50 mg”, “Show XX O”, and “Sari XX Ointment”, When touching the “OOXX ointment” button 19j, the drug name of “SariOOXX ointment” is excluded from the dispensing audit target, and “AlOO tablet 10 mg”, “Selve OO50 mg”, Dispensing audits are performed for three types of drugs 2, A drug 2a, B drug 2b, and C drug 2c, each having the drug name “Show XXX”.

In other words, the touch panel type operation unit 19 in a state of displaying the audit exclusion medicine setting screen has an audit exclusion medicine setting in which a prescription medicine to be excluded from the dispensing audit target can be freely selected from a plurality of kinds of prescription medicines in the prescription information. It functions as a part.
Then, the dispensing suitability determination unit P2 determines the suitability of the dispensing contents for the prescription drugs excluding the prescription drugs set in the audit exclusion drug setting unit among the plural types of prescription drugs in the prescription information. It will be configured.

  In the dispensing inspection process, the dispensing suitability determining means P2 reads the weight corresponding to the prescription quantity of the prescription drug to be dispensed from the packaging unit number / weight relationship information in the storage device 11. When there are multiple types of prescription drugs, for each of the multiple types of prescription drugs, the weight corresponding to the prescription quantity for each prescription drug is read from the number of packaging units vs. weight relation information, and each prescription drug is read The total weight is integrated, and the integrated value is taken as the total prescription drug weight. The dispensing suitability determination means P2 is for dispensing suitability determination with the weight obtained by subtracting the allowable range setting value from the total prescription drug weight as the lower limit value and the weight obtained by adding the allowable range setting value to the total prescription drug weight as the upper limit value. Set the gross weight tolerance. The allowable range setting value is set in advance to a predetermined value (for example, 1 mg) and stored in an internal memory (not shown) of the central control device C.

Subsequently, the dispensing suitability determination unit P2 compares the total weight of the drug assembly, which is the weighing data of the weighing device 17, and the total weight allowable range, and the drug name determined by the drug name determination unit P1 and the dispensing audit. Compare the name of the prescription drug set as the target. Then, the dispensing suitability determining means P2 determines that the total weight of the drug assembly is within the total weight allowable range and that the drug name determined by the drug name determining means P1 matches the name of the prescription drug. Although the illustration is omitted, the display device 13 displays a dispensation appropriate notice screen with a message indicating that the dispensation is appropriate, for example, “Dispensing is appropriate”. On the other hand, if either one is not established or neither is established, the illustration is omitted, but for example, dispensation inappropriate notification by a message indicating that the dispensing is inappropriate, such as “Dispensing is inappropriate” The screen is displayed on the display device 13.
It should be noted that the “screen switching” button 19f similar to that shown in FIGS. 10 and 11 is displayed on the dispensing appropriateness notification screen and the dispensing inappropriateness notification screen, and when this “screen switching” button 19f is touched, FIG. Is displayed on the display device 13.

  When a plurality of types of drug assemblies 1 are placed on the examination table 15, the weighing device 17 measures the total weight of the plurality of types of drug assemblies 1, and determines the total weight of the plurality of types of drug assemblies 1. It is determined whether or not the weighing data is within the total weight allowable range, and whether or not the plurality of drug names determined by the drug name determination unit P1 matches the names of a plurality of types of prescription drugs set as dispensing inspection targets. Is determined.

When the “individual drug name determination mode” button 19c is touched on the initial screen shown in FIG. 9, the dispensing suitability determination means P2 executes the individual drug name determination mode as follows.
That is, when the “individual drug name determination mode” button 19c is touched and the weighing data of the weighing device 17 decreases, the dispensing suitability determining means P2 first increases the decrease value of the weighing data of the weighing device 17 and sets the drug weight. To do.
Subsequently, the dispensing propriety determination means P2 determines the names of a plurality of prescription drugs read in the previous dispensing audit process (excluded from the dispensing audit target on the audit exclusion medicine setting screen) from the information on the number of packaging units versus weight in the storage device 11. The weight corresponding to the prescription quantity is read as the prescription weight for each drug, and the weight obtained by subtracting the allowable range setting value from the prescription weight for each drug is set as the lower limit value. A drug-specific weight tolerance range for determining the suitability of dispensing is set with a weight obtained by adding the tolerance range setting value to the upper limit.

Subsequently, the dispensing suitability determination unit P2 determines whether there is a drug weight within the permissible range among the permissible weights set for each of the plurality of types of prescription drugs, and the determination result. Is displayed on the display device 13.
That is, if there is a drug weight that falls within the allowable range among the drug-specific weight tolerance ranges set for each of a plurality of types of prescription drugs, for example, the drug name “Selve XX50 mg” When the corresponding drug-specific weight tolerance is entered, the illustration of the individual drug name discrimination result notification screen is omitted, but for example, “the lifted drug is“ Selve XX50 mg ””, for example, A screen showing the medicine name corresponding to the allowable range is displayed on the display device 13. On the other hand, if not, the illustration of the individual drug name determination result notification screen is omitted, but the lifted drug assembly 1 is improperly dispensed, for example, “the lifted drug does not match the prescription content”. The display device 13 displays a screen indicating that the medicine is a drug.
Although illustration is omitted, the “screen switching” button 19f is also displayed on the individual medicine name discrimination result notification screen.

That is, the individual medicine name discrimination mode is a mode in which one kind of medicine assembly 1 is lifted from the plurality of kinds of medicine assemblies 1 placed on the examination table 15 and the medicine name of the lifted medicine assembly 1 is discriminated. The “individual drug name discrimination mode” button 19b of the touch panel type operation unit 19 functions as a mode command unit that commands execution of the individual drug name discrimination mode.
Then, when the individual drug name discrimination mode is commanded by the “individual drug name discrimination mode” button 19b and the weighing data of the weighing device 17 decreases, the dispensing suitability determination means P2 executes the individual drug name discrimination mode. It will be configured.
And in the individual medicine name discrimination mode, the dispensing suitability judging means P2 uses the number of packaging units corresponding to the prescription quantity of the medicine for each of a plurality of kinds of prescription medicines based on the number of packaging units vs. weight relation information and prescription information. The prescription weight for each drug, which is the weight of the drug, and set the permissible weight range for each drug based on the prescription weight for each drug, and raise the decrease value of the weighing data of the weighing device 15 as the drug weight , It is determined whether or not there is a lifting drug weight that falls within the allowable range among the drug-specific weight tolerances set for each of multiple types of prescription drugs, and if there is, it corresponds to the drug-specific weight tolerance The medicine name to be output is output to the display device 13, and when there is no medicine, the information indicating that the lifted medicine assembly 1 is an inappropriately dispensed medicine is output to the display device 13. It becomes Rukoto.

When the number of packaging bodies 4 (ie, the number of packaging units) is larger than the number of packaging bodies 4 constituting the collective packaging body 5 in the information on the number of packaging units versus weight in the storage device 11, The set rubber band weight is added to the weight set corresponding to the number.
Therefore, when the prescription quantity included in the prescription information is larger than the number of the packaging bodies 4 constituting the collective packaging body 5, the medicine-specific prescription weight obtained by the dispensing suitability determining means P2 is a weight obtained by adding the set rubber band weight. It is.
That is, the number of the packages 4 constituting the collective package 5 is set to the set prescription quantity for adding the rubber band weight. When the prescription quantity included in the prescription information is equal to or greater than the set prescription quantity for adding the rubber band weight, the prescription of the drug is determined for each of a plurality of types of prescription drugs under the condition of adding the set rubber band weight. The medicine-specific prescription weight, which is the weight in the number of packaging units corresponding to the quantity, is obtained, and the total prescription medicine weight is obtained based on the obtained medicine-specific prescription weight.

Next, the control operation of the central controller C will be described based on the flowchart shown in FIG. In addition, description of “ON” of each button of the touch panel type operation unit 19 in the flowchart corresponds to touching each button.
When an operation switch (not shown) is turned on, an initial screen is displayed on the display device 13 (step # 1).
Subsequently, when the “prescription information import” button 19d is touched on the initial screen, the prescription information is fetched, and when the “audit exclusion medicine setting” button 19b is touched, the audit exclusion medicine setting screen is displayed. When the “screen switching” button 19f is touched and the “audit exclusion medicine setting” button 19b is not touched, the “dispensing inspection” button 19a is touched or the “individual medicine name discrimination mode” button is touched. Wait for 19c to be touched (steps # 2-8).
When the “Dispensing Audit” button 19a is touched, the name of the prescription drug subject to the dispensing audit as described above depending on whether the “prescription information import” button 19d is touched first or not, as described above. And the medicine name discrimination process is executed (steps # 7 and 9).

In the drug name discrimination process of step # 9, when the drug names can be discriminated for all the drug assemblies 1, the dispensing audit process is executed as described above to determine whether the dispensing contents are appropriate or not. Is displayed, the dispensing proper notification screen is displayed on the display device 13. On the other hand, if the dispensing content is not proper, the dispensing inappropriate notification screen is displayed on the display device 13, and then the “screen switching” button 19 f is displayed. When touched, the process returns (steps # 10 to 14, 6).
On the other hand, in the drug name determination process of step # 9, if the drug names cannot be determined for all drug assemblies 1, a drug name rejection determination screen is displayed on the display device 13, and the “screen switching” button 19f is touched. If it is done, the process returns (steps # 10, 15, 6).

  When the “individual drug name discrimination mode” button 19c is touched on the initial screen, the individual drug name discrimination mode is executed as described above, and the individual drug name discrimination result notification screen is displayed based on the discrimination result. 13 and then, when the “screen switching” button 19f is touched, the process returns (steps # 8, 16, 17, 6).

  When the “audit exclusion medicine setting” button 19b is touched on the initial screen, the process proceeds to step # 5. When the “dispensing inspection” button 19a is touched on the initial screen, the process proceeds to step # 9.

Next, the procedure of the dispensing operation performed by the dispensing operator will be described.
The dispensing operator collects the drug assembly 1 based on the prescription information described in the prescription, but when there are a plurality of types of prescription drugs, as shown in FIG. Collect multiple types of drug assembly 1. Further, when the collected drug assembly 1 is composed of a plurality of assembly packages 5 or a combination of the assembly package 5 and the fraction assembly package 5h, they are bundled together with a rubber band 6.
Then, as shown in FIG. 8, a plurality of types of drug assemblies 1 are placed on the dispensing tray 26, and the dispensing tray 26 is placed on the inspection table 15 of the drawer 21 that is pulled out from the casing 20, and then the drawer 21 is pushed in and stored in the casing 20. Also, a prescription for dispensing inspection is set in the input device 12 and the “prescription information import” button 19d on the initial screen is touched.
When there are prescription drugs that are excluded from the dispensing audit target among the prescription drugs described in the prescription, touch the “audit excluded drug setting” button 19b on the initial screen to select a drug to be excluded from the dispensing audit target. Set.

Subsequently, when the “Dispensing Audit” button 19a on the initial screen is touched, a medicine name discrimination process is executed, and in the medicine name discrimination process, when all the drug names of the plurality of types of drug assemblies 1 are discriminated, The audit process is executed, and either the appropriate dispensing notification screen or the inappropriate dispensing notification screen is displayed on the display device 13.
When the dispensing proper notification screen is displayed on the display device 13, it can be seen that the content of the dispensing was appropriate.
When the dispensing inappropriate notification screen is displayed on the display device 13, the drawer unit 21 is pulled out, and a predetermined one is lifted and taken out from the plurality of types of drug assemblies 1. The container 20 is stored in the casing 20, and the “individual drug name discrimination mode” button 19c on the initial screen is touched.
Then, the individual drug name discrimination mode is executed and the individual drug name discrimination result notification screen is displayed on the display device 13, so that it can be determined whether or not the content of the dispensed drug assembly 1 is appropriate. Then, the individual drug name discrimination mode is executed for all of the plurality of types of drug assemblies 1 to find the drug assembly 1 having an inappropriate dispensing content among the plurality of types of drug assemblies 1. Can be corrected.

On the other hand, in the drug name determination process, when all of the drug names of the plurality of types of drug aggregates 1 cannot be determined, a display screen for displaying the drug name as shown in FIG. Therefore, the dispensing operator pulls out the drawer 21 and changes the posture by inverting or changing the direction of the drug assembly 1 corresponding to the image that “cannot be determined”, and then again, The drawer 21 is housed in the casing 20 and the “Dispensing Audit” button 19a on the initial screen is touched.
Then, the medicine name discrimination process is executed again. If the drug names of all the plural types of drug aggregates 1 are discriminated in the medicine name discrimination process, the dispensing audit process is executed.
As described above, even when a plurality of types of medicines are prescribed, the dispensing inspection work can be performed efficiently.

[Second Embodiment]
Hereinafter, a second embodiment of the present invention will be described with reference to FIGS. 13 to 19. This second embodiment mainly includes the configurations of the inspection table 15 and the weighing device 17 and the control of the central control device C. Another embodiment of the operation will be described. Therefore, the inspection table 15 and the weighing device 17 are mainly described in the entire configuration of the dispensing inspection system, and the other components are denoted by the same reference numerals as those in the first embodiment and the description thereof is omitted. Further, regarding the control operation of the central controller C, mainly the control operation different from the first embodiment will be described.

In the second embodiment, as shown in FIGS. 13 to 15, the examination table 15 is divided into a plurality of placement sections 15 d on which a plurality of types of drug assemblies 1 can be placed by type, and a weighing device. 17 is provided corresponding to each placement section 15d, and includes a plurality of section weighing sections 17d capable of weighing the weight of the drug assembly 1 placed in each placement section 15d. .
Further, each of the plurality of placement sections 15d is configured to include a base portion 15s protruding above the peripheral portion of each placement section 15d, and each section weighing portion 17d weighs a load applied to each base portion 15s. Is configured to do.

As shown in FIGS. 16 to 18, a plurality of storage compartments 29 d that can be placed on the examination table 15 and can accommodate a plurality of types of drug assemblies 1 by type correspond to a plurality of placement compartments 15 d. A dispensing tray 29 is provided as an inspection tray.
The dispensing tray 29 forms a tray main body 29m having a square cylindrical portion 29f as a frame portion for dividing and forming a plurality of storage compartments 29d, and a bottom portion of each storage compartment 29d, and in each storage compartment 29d, a square tube And a mounting plate 29p provided in each housing section 29d so as to be relatively movable in the vertical direction with respect to the shape portion 29f, and as the tray body 29m is mounted on the inspection table 15, Each mounting plate 29p is lifted by each base part 15s, and is mounted and supported on each base part 15s.

  As shown in FIGS. 14, 15, and 18, the base portion 15 s is a rectangular trapezoidal shape in a plan view, and six base portions 15 s are arranged in the front-rear direction and three in the left-right direction. And it is provided on the inspection table 15 in a state where a lattice-shaped groove portion 15g is formed with an interval between adjacent ones in front and rear and right and left.

  A load detection sensor (for example, a load cell) that constitutes each section weighing section 17d of the weighing device 17 is provided so as to apply a load on each section 15s of the inspection table 15, and each section weighing section 17d is provided with this load detection sensor. Based on this detection signal, the load applied to each base 15s is weighed.

As shown in FIGS. 16 to 18, the rectangular tubular portion 29 f is in a constricted shape that becomes narrower downward, and six square tubular portions 29 f are arranged in the front-rear direction and three in the left-right direction. The tray main body 29m is provided in a state where the upper end portions are aligned and connected.
A square frame-shaped receiving portion 29h is provided at the lower end opening of each square tubular portion 29f so as to protrude inward.
Each mounting plate 29p is provided in each receiving section 29d in a state of being received by each receiving portion 29h.

Then, as shown in FIG. 18, as the dispensing tray 29 is placed on the inspection table 15, the plurality of rectangular cylindrical portions 29 f of the dispensing tray 29 fit into the lattice-shaped grooves 15 g of the inspection table 15. In addition, each mounting plate 29p of the dispensing tray 29 is lifted by each table portion 15s of the inspection table 15 and is mounted and supported on each table portion 15s.
In performing a dispensing audit of a dispensed medicine, a dispensing tray 29 containing a plurality of medicine assemblies 1 divided into a plurality of placement sections 29d is placed on the inspection table 15. Although not shown in the drawing, the portion 17d has a function of canceling the tare such as the mounting plate 29p. Therefore, by canceling the tare, when the dispensing tray 29 storing the plurality of medicine assemblies 1 divided into the plurality of placement sections 29d is placed on the inspection table 15, the weights of the plurality of medicine assemblies 1 are individually set. Can be weighed.

In the second embodiment, the configurations of the medicine name determination unit P1 and the dispensing suitability determination unit P2 are different from those of the first embodiment and are configured as follows.
That is, in the medicine name discrimination process, the medicine name discrimination means P1 discriminates the medicine names of the plurality of types of medicine aggregates 1 placed on the examination table 15 in correspondence with the placement sections 15d. It is configured.
In addition, the dispensing suitability determination means P2 is configured to determine the suitability of the contents of dispensing by using the total of the weighing results of the plurality of section weighing units 17d as the total weight of the drug assembly in the dispensing audit process, If the weight is not within the total weight tolerance, based on the number of packaging units vs. weight relationship information and prescription information, for each of several types of prescription drugs, it is the weight in the number of packaging units corresponding to the prescription quantity of the drug A prescription weight is obtained, and a weight tolerance range for determining the suitability of dispensing is set based on the prescription weight for each medicine, and among the plurality of placement sections 29d, the section weighing unit 17d of each placement section 29d is set. When the weight of the weighed drug assembly is not within the permissible drug weight corresponding to the drug name determined corresponding to the placement section 15d, the determination result is displayed on the display device 13. To output It has been made.

Hereinafter, explanation will be given on the medicine name discrimination processing by the medicine name discrimination means P1 and the dispensing inspection processing by the dispensing suitability judgment means P2.
The medicine name determination means P1 omits the illustration when the drug names cannot be determined for all of the plural kinds of drug assemblies 1 placed on the examination table 15, but the display device 13 displays “No drug name The “Determination screen” is displayed. In this “drug name rejection determination screen”, for example, information related to the placement section 29d in which the drug name cannot be determined, such as “the name of the second drug from the left and the first drug from the front cannot be determined” is displayed.

When the dispensing inspection system is activated, an initial screen is displayed on the display device 13 as in the first embodiment. Although not shown, a “Dispensing Audit” button 19a, an “Audit Excluded Medicine Setting” button 19b, a “Prescription Information Import” button 19d, and an “End” button 19e are displayed on the display screen, as shown in FIG. The “individual drug name discrimination mode” button 19c on the initial screen in the first embodiment is not displayed.
Since the control operation when the “audit exclusion medicine setting” button 19b, the “prescription information import” button 19d, and the “end” button 19e are touched is the same as that in the first embodiment, description thereof will be omitted.

When the “Dispensing Audit” button 19a is touched, the dispensing propriety determination means P2 sets the name of the prescription drug subject to the dispensing audit and sets the prescribed prescription drug targeted for the dispensing audit, as in the first embodiment. Based on the prescription information about the dispensing audit process.
In the dispensing inspection process, the dispensing suitability determination unit P2 reads the weight corresponding to the prescription quantity for the prescription drug to be dispensed from the packaging unit number / weight relationship information in the storage device 11, and is the same as in the first embodiment. In addition, the total weight of the prescription drug is obtained, and a total weight allowable range is set, and the total of the weighing results of the plurality of compartment weighing units 17d is set as the total weight of the drug assembly.
The dispensing suitability determining unit P2 compares the total weight of the drug assembly with the total weight allowable range, and determines the drug name determined by the drug name determining unit P1 and the name of the prescription drug included in the prescription information. Compare. Then, the dispensing suitability determination means P2 both has the total weight of the drug assembly within the total weight allowable range and that the medicine name determined by the medicine name determination means P1 matches the name of the prescription drug. Is established, a dispensation appropriate notice screen with a message indicating that the dispensing is appropriate, such as “Dispensing is appropriate”, is displayed on the display device 13.

  On the other hand, if the medicine name determined by the medicine name determining means P1 and the name of the prescription drug included in the prescription information do not match, the dispensing suitability determination means P2 is the name of the prescription medicine among the determined medicine names. The placement section 29d corresponding to the one not included in the is specified. Although not shown, for example, the location of the placement section 29d where the drug name is not appropriate and the reason why the dispensing is not appropriate (name, such as “the drug name of the second drug from the left in the front row is inappropriate”) A name improper notification screen indicating “improper” is displayed on the display device 13.

Also, the dispensing suitability determining means P2 determines that the total weight of the drug assembly is within the total weight allowable range even if the drug name determined by the drug name determining means P1 matches the name of the prescription drug included in the prescription information. If not, the weight corresponding to the prescription quantity for each prescription drug subject to dispensing audit read from the information on the number of packaging units in the storage device 11 and the weight is used as the prescription weight for each medicine, and allowed from the prescription weight for each medicine. A weight tolerance range for determining the suitability of dispensing is set, with the weight obtained by subtracting the range setting value as the lower limit value and the weight obtained by adding the tolerance range setting value to the drug-specific prescription weight as the upper limit value.
Subsequently, the dispensing suitability determination unit P2 corresponds to the weight of the drug assembly 1 weighed by the section weighing unit 17d of each placement section 29d and the placement section 15d for each of the plurality of placement sections 29d. The placement weight 29d in which the weight of the medicine assembly 1 is not within the weight tolerance for each medicine is judged by comparing with the weight tolerance for each medicine corresponding to the determined medicine name.
The dispensing suitability determination unit P2 omits the illustration as the determination result, but the placement section 29d whose quantity is not appropriate is, for example, “the quantity of the second medicine from the left in the front row is inappropriate”. The display device 13 displays a quantity inappropriateness notification screen indicating the location of the item and the reason why the dispensing is not appropriate (quantity inappropriate).

Next, the control operation of the central controller C will be described based on the flowchart shown in FIG.
When an operation switch (not shown) is turned on, an initial screen is displayed on the display device 13 (step # 21).
Subsequently, when the “prescription information import” button 19d is touched on the initial screen, the prescription information is fetched, and when the “audit exclusion medicine setting” button 19b is touched, the audit exclusion medicine setting screen is displayed. When the “screen switching” button 19f is touched, and when the “audit exclusion medicine setting” button 19b is not touched, the “dispensing inspection” button 19a is touched (steps # 22 to 27). .
When the “Dispensing Audit” button 19a is touched, the name of the prescription drug subject to the dispensing audit is set as described above depending on whether the “prescription information import” button 19d is touched or not touched, respectively. Then, a medicine name discrimination process is executed (step # 28).

In the drug name determination process in step # 28, when the drug names can be determined for all drug assemblies 1, the dispensing audit process is executed as described above to determine whether the dispensing contents are appropriate. When the content of the dispensing is appropriate, a proper dispensing notification screen is displayed on the display device 13, and when the content of the dispensing is not appropriate due to a drug name not matching, the name inappropriate notification screen is displayed on the display device 13. If the dispensing contents are not appropriate because the quantities do not match, the quantity improper notification screen is displayed on the display device 13, and then, when the “screen switching” button 19f is touched, the process returns (step # 29-35, 26).
On the other hand, in the drug name determination process of step # 28, if the drug names cannot be determined for all drug assemblies 1, a drug name rejection determination screen is displayed on the display device 13, and the “screen switching” button 19f is touched. Then, the process returns (steps # 29, 36, 26).

Next, the procedure of the dispensing operation performed by the dispensing operator will be described.
Similarly to the first embodiment, when there are a plurality of types of prescription drugs, the dispensing operator collects a plurality of types of drug assemblies 1 corresponding to the plurality of types of prescription drugs. Then, as shown in FIG. 16, the collected plural kinds of drug aggregates 1 are classified according to type and accommodated in a plurality of accommodating sections 29 d of the dispensing tray 29, and the dispensing tray 29 is drawn out from the casing 20. Then, the drawer 21 is pushed in and stored in the casing 20. Also, a prescription for dispensing inspection is set in the input device 12 and the “prescription information import” button 19d on the initial screen is touched.
When there are prescription drugs that are excluded from the dispensing audit target among the prescription drugs described in the prescription, touch the “audit excluded drug setting” button 19b on the initial screen to select a drug to be excluded from the dispensing audit target. Set.

Subsequently, when the “Dispensing Audit” button 19a on the initial screen is touched, a medicine name discrimination process is executed. In the drug name determination process, when all the drug names of the plurality of types of drug aggregates 1 are determined, a dispensing audit process is executed. If the dispensing contents are appropriate, the display device 13 Announcement screen is displayed.
On the other hand, if the content of the dispensing is not appropriate, the display device 13 displays either the name improper notice screen or the quantity improper notice screen.
And the dispensation operator can correct the dispensation content of the medicine assembly 1 in the corresponding placement section 15d based on the display content of the name improper notification screen or the quantity improper notification screen.

In the drug name discrimination process, when all of the drug names of the plurality of types of drug aggregates 1 cannot be discriminated, a drug name denial discrimination screen is displayed on the display device 13, and the “medicine name denial discrimination screen” indicates which It can be seen that the drug name of the drug assembly 1 in the placement section 15d could not be determined.
Thus, as in the first embodiment, the dispensing operator pulls out the drawer 21 and changes the posture by inverting or changing the direction of the drug assembly 1 in the corresponding placement section 15d. After that, the drawer 21 is housed in the casing 20 again, and the “Dispensing Audit” button 19a on the initial screen is touched.
Then, the medicine name discrimination process is executed again. If the drug names of all the plural types of drug aggregates 1 are discriminated in the medicine name discrimination process, the dispensing audit process is executed.
As described above, even when a plurality of types of medicines are prescribed, the dispensing inspection work can be performed efficiently.

[Another embodiment]
Next, another embodiment will be described.
(A) In the above-described embodiment, a function of setting one to be excluded from the dispensing audit target among a plurality of prescription drugs in the prescription information is provided by displaying the “audit exclusion drug setting” button 19b on the initial screen. However, such an “excluded medicine setting” button 19b may be omitted and all prescription medicines in the prescription information may be subject to dispensing audits.

(B) In the medicine 2 such as a tablet or capsule, the medicine name or medicine code may be displayed on the medicine 2 itself by printing or engraving.
In such a case, the medicine name discriminating means P1 identifies either the medicine name or medicine code displayed on the medicine 2 in addition to the medicine name or medicine code printed on the packaging material 3. The medicine name may be discriminated.

(C) The load detection sensor constituting the weighing device 17 is not limited to the load cell exemplified in the above embodiment, and for example, a tuning fork type sensor can be used.

(D) The specific configuration of the input device 12 is not limited to the OCR exemplified in the above embodiment. For example, a configuration that is input via a LAN in a hospital or a configuration that is input via a receipt computer that manages information in a dispensing pharmacy may be used. Alternatively, it may be configured to input manually by using a keyboard or the like.

(E) In the first embodiment, the dispensing tray 26 may be omitted, and a plurality of types of drug assemblies 1 may be directly placed on the examination table 15. Moreover, in said 2nd Embodiment, it is good also as a structure which abbreviate | omits the dispensing tray 29 and mounts the some chemical | medical agent assembly 1 directly on the some base part 15s according to a kind.

(F) The specific configuration of the determination result output unit is not limited to the display device 13 illustrated in the above embodiment, and may be a speaker, for example.

(G) As a so-called image recognition format in which the drug name is determined by the drug name determination unit P1 based on the imaging information of the imaging device 16, various known formats can be used.

DESCRIPTION OF SYMBOLS 1 Drug assembly 2 Drug 3 Packaging material 4 Packaging unit 11 Storage means 12 Prescription information input means 13 Determination result output means, image display means 15 Examination table 15d Mounting section 15s Stand section 16 Imaging means 17 Weighing means 17d Section weighing section 19c Mode command part 29 Inspection tray 29d Storage section 29f Frame part 29m Tray body 29p Placement plate P1 Drug name determination means P2 Dispensing suitability determination means

Claims (6)

Packing unit number vs. weight relation information indicating the relationship between the number of packaging units and the weight, which is the number of drugs in the packaging unit packaged in the packaging material, the drug code corresponding to multiple drug names or multiple drug names Storage means for storing in association with each of the
Prescription information input means for inputting prescription information including the name of the prescribed prescription drug and the prescription quantity;
An examination table for placing a drug assembly in which the drugs are collected in a state of being packaged in a packaging material based on the prescription information as a drug to be dispensed,
Imaging means for imaging the drug assembly placed on the examination table;
Based on the imaging information of the imaging means, drug name determination means for determining the drug name of the drug assembly placed on the examination table,
Weighing means for weighing the weight of the drug assembly placed on the examination table;
Based on the prescription information input by the prescription information input means, the number-of-packaging unit-weight relation information stored in the storage means, the drug name determination result by the drug name determination means, and the weighing data of the weighing means Dispensing propriety determination means for determining the propriety of the dispensing contents including the drug name of the drug assembly and the quantity of the drug,
A dispensing audit system provided with a determination result output means for outputting a determination result by the dispensing suitability determination means,
In the case where a plurality of types of drug assemblies are mounted on the examination table, the drug name determination unit is configured to be able to determine the drug names for each of the plurality of types of drug assemblies,
The dispensing suitability determining means is
If the prescription information includes the names of a plurality of types of prescription drugs, the weight in the number of packaging units corresponding to the prescription quantity in the plurality of types of prescription drugs based on the information on the number of packaging units versus weight and the prescription information The total weight of the prescription drugs, and a total weight tolerance range for determining the propriety of dispensing based on the total weight of the prescription drugs, and the total of a plurality of types of drug aggregates weighed by the weighing means The total weight of the drug assembly, which is the weight, is within the total weight allowable range, and the plurality of drug names determined by the drug name determining means match the names of a plurality of types of prescription drugs included in the prescription information Then, it is configured to output information indicating that the dispensing content is appropriate to the determination result output unit ,
A mode command section for instructing execution of an individual drug name discrimination mode for lifting a kind of drug aggregate from a plurality of kinds of drug aggregates placed on the examination table and discriminating the drug name of the lifted drug aggregate Is provided,
The dispensing suitability determining means is
When the individual medicine name discrimination mode is commanded by the mode command section and the weighing data of the weighing means is reduced, the individual medicine name discrimination mode is executed,
In the individual drug name discrimination mode, the prescription by drug, which is the weight in the number of packaging units corresponding to the prescription quantity of the medicine, for each of a plurality of types of prescription medicines based on the information on the number of packaging units versus weight and the prescription information In addition to obtaining the weight, a drug-specific weight tolerance range for determining the suitability of dispensing is set based on the drug-specific prescription weight, and a decrease value of the weighing data of the weighing means is raised as a drug weight, and each of a plurality of types of prescription drugs It is determined whether or not there is any drug weight tolerance range set for the drug whose lifting drug weight falls within the tolerance range. If there is, the drug name corresponding to the drug weight tolerance range is determined as described above. and outputs the result output means, if not, adjusting the lifting drug aggregates are constituted of information indicating that the improperly formulated drug to output the determination result output unit Audit system. Packing unit number vs. weight relation information indicating the relationship between the number of packaging units and the weight, which is the number of drugs in the packaging unit packaged in the packaging material, the drug code corresponding to multiple drug names or multiple drug names Storage means for storing in association with each of the
Prescription information input means for inputting prescription information including the name of the prescribed prescription drug and the prescription quantity;
An examination table for placing a drug assembly in which the drugs are collected in a state of being packaged in a packaging material based on the prescription information as a drug to be dispensed,
Imaging means for imaging the drug assembly placed on the examination table;
Based on the imaging information of the imaging means, drug name determination means for determining the drug name of the drug assembly placed on the examination table,
Weighing means for weighing the weight of the drug assembly placed on the examination table;
Based on the prescription information input by the prescription information input means, the number-of-packaging unit-weight relation information stored in the storage means, the drug name determination result by the drug name determination means, and the weighing data of the weighing means Dispensing propriety determination means for determining the propriety of the dispensing contents including the drug name of the drug assembly and the quantity of the drug,
A dispensing audit system provided with a determination result output means for outputting a determination result by the dispensing suitability determination means,
In the case where a plurality of types of drug assemblies are mounted on the examination table, the drug name determination unit is configured to be able to determine the drug names for each of the plurality of types of drug assemblies,
The dispensing suitability determining means is
If the prescription information includes the names of a plurality of types of prescription drugs, the weight in the number of packaging units corresponding to the prescription quantity in the plurality of types of prescription drugs based on the information on the number of packaging units versus weight and the prescription information The total weight of the prescription drugs, and a total weight tolerance range for determining the propriety of dispensing based on the total weight of the prescription drugs, and the total of a plurality of types of drug aggregates weighed by the weighing means The total weight of the drug assembly, which is the weight, is within the total weight allowable range, and the plurality of drug names determined by the drug name determining means match the names of a plurality of types of prescription drugs included in the prescription information Then, it is configured to output information indicating that the dispensing content is appropriate to the determination result output unit,
The examination table is divided into a plurality of placement sections that can be placed by dividing a plurality of types of drug aggregates by type,
The weighing means is provided corresponding to each placement section, and the medicine placed on each placement section
It comprises a plurality of compartment weighing units that can weigh the aggregate,
The drug name determination means is configured to determine the drug name of each of a plurality of types of drug assemblies placed on the examination table in association with each of the plurality of placement sections,
The dispensing suitability determining means is
The total of the weighing results of the plurality of compartment weighing units is used as the total weight of the drug assembly, and is configured to determine the suitability of the contents of dispensing, and
When the total weight of the drug assembly is not within the total weight allowable range, the packaging unit corresponding to the prescription quantity of the drug for each of a plurality of types of prescription drugs based on the information on the number of packaging units versus the weight and the prescription information The prescription weight for each medicine, which is a weight in number, is determined, and the weight tolerance for each medicine for determining the suitability of dispensing is set based on the prescription weight for each medicine. The weight of the drug assembly weighed in the section weighing section of the section is determined to be not within the weight tolerance range for each drug corresponding to the drug name determined corresponding to the placement section, and the determination result is determined. A dispensing inspection system configured to output to the determination result output means . Each of the plurality of placement sections is configured to include a base portion that protrudes upward from the peripheral portion of each placement section,
Each compartment weighing unit is configured to weigh the load applied to each platform,
An inspection tray that can be placed on the examination table and includes a plurality of storage compartments corresponding to the plurality of placement compartments that can contain a plurality of types of drug aggregates by type, and is provided.
The inspection tray forms a tray main body having a frame section for dividing and forming the plurality of storage sections, and forms a bottom portion of each storage section, and is relatively movable in the vertical direction with respect to the frame section in each storage section. Each of the receiving sections is provided with a mounting plate, and each mounting plate is lifted by each base portion as the tray body is mounted on the inspection table. The dispensing inspection system according to claim 2 , wherein the dispensing inspection system is configured to be placed and supported by the unit . Image display means for displaying an image picked up by the image pickup means is provided;
When there is a drug assembly whose drug name cannot be identified among a plurality of types of drug assemblies placed on the examination table, the drug name determination unit displays the drug name on the image display unit. The dispensing audit system according to any one of claims 1 to 3, wherein the dispensing audit system is configured to display information indicating that a drug name cannot be identified in association with an image of a drug assembly that cannot be identified . When the prescription quantity included in the prescription information is equal to or greater than the set prescription quantity for adding the rubber band weight, the prescription quantity of the drug for each of a plurality of types of prescription drugs under the condition for adding the set rubber band weight The prescription weight according to medicine which is the weight in the number of packaging units corresponding to the above is obtained, and the total weight of the prescription medicine is obtained based on the obtained prescription weight by medicine. Dispensing audit system according to item. From the imaging information of the imaging means, the medicine name discriminating means displays the medicine name displayed on the medicine and the medicine code corresponding to the medicine name, and the medicine name and medicine name displayed on the packaging material packaging the medicine. The dispensing audit system according to any one of claims 1 to 5, wherein the dispensing inspection system is configured to identify any one of the medicine codes corresponding to the name and determine the medicine name .

Images