JPH06345003A - Controller for medicine packing device - Google Patents

Abstract

PURPOSE:To display all types of medicine to be given to a patient on a display screen of a CRT and apply an identifier such as a mark to types of medicine which cannot be packed in a packing device. CONSTITUTION:A controller for a medicine packing device comprises medicine file memories M11 to M1n for storing types of medicine to be registered and information as to whether the types of medicine can be packed in addition to a central processor 18 and a key input part 12 for extracting the types of medicine to be given to a patient from the types stored in the medicine file memories and also inputting the number of types of medicine. It comprises the central processor 18 for identifying a type of medicine which cannot be packed in the packing device 11 based on the information as to whether it can be packed and a CRT 22 for displaying the extracted types of medicine to be given to the patient, so that the types of medicine which cannot be packed among those displayed on the CRT are marked.

Description

Detailed Description of the Invention

[0001]

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a control device for a medicine packing machine capable of selectively packing one or several kinds of medicines in a hospital or the like based on a prescription different for each patient.

[0002]

2. Description of the Related Art A medicine packaging machine is disclosed in, for example, Japanese Patent Laid-Open No. 59-77.
As disclosed in Japanese Patent No. 568, a patient's past prescription is called, and based on the called past prescription, predetermined prescription information is classified into information to be processed by a medicine packaging machine and other information, and this packaging is performed. The information that can be processed by the machine is stored in the A file, the information that cannot be processed by the packaging machine is stored in the B file, and the prescription information stored in the A file is packaged by the medicine packaging machine.

[0003]

However, since the medicine packing machine displays only the A file when the medicine packing machine packs the medicine, the prescription information of the B file which cannot be packed by the medicine packing machine is stored in the medicine packing machine. There was a problem that it could not be processed during the packaging work of the machine.

The present invention solves the above problems,
It is an object of the present invention to provide a control device for a medicine packaging machine, which displays all the medicine types to be administered on a display device and has a mark or the like for identifying a medicine type that cannot be packaged by the medicine packaging machine.

[0005]

According to the present invention, a drug type to be registered and a means for storing packaging availability information of this drug type, and a drug type to be administered from the drug types stored in this storage means are stored. A means for extracting and inputting the number of medicines of this medicine type, a means for discriminating a medicine type that cannot be packaged in the packaging machine based on the medicine packaging availability information, and a means for displaying the extracted medicine type to be administered And a mark is attached to a non-packable drug type among the drug types displayed on the display means.

[0006]

With the above-described structure, the control device for the medicine packaging machine of the present invention can store the information as to whether or not the medicine type to be registered can be packaged. When the medicine type and the number of medicines are input during the packaging, the display device is displayed. In addition to displaying all the drug types to be dispensed on the packaging machine, detect the drug types that cannot be packaged by the packaging machine, and notify the worker by attaching a mark etc. to identify the drug types that cannot be packaged. It was done like this.

[0007]

EXAMPLE FIG. 1 shows an external view of a tablet packing machine, which comprises an operating device (10) and a packing machine (11). The operating device (10) creates prescription data by key operation of the key input unit (12) and transfers it to the packaging machine (11), and the packaging machine (1)
1) performs the packaging operation based on the transferred prescription data.

FIG. 2 shows the construction of the packaging machine (11), in which a tablet case storage section (1) is formed in the upper part, and below the hopper (2), the shutter (3) and the tablet packing mechanism (4). Are arranged. The tablet case (1) has a tablet case (5) according to the type of tablet.
... (5) is placed on the tablet case (5) ...
(5) is configured to be driven by the input of a predetermined extraction signal to extract a tablet and introduce it into the hopper (2) through a drop passage (not shown). The tablet wrapping mechanism (4) is heat-sealable, and the roller (7) around which the wrapping paper (6) previously folded in two is wound, the tension roller (8), and the wrapping paper (6) are heat-sealed vertically. Vertical heat-sealing mechanism (9) for forming continuous pouches, and horizontal heat-sealing mechanism (1) for sealing the upper opening of the pouch in which the tablets are loaded.
0) and a feed roller (11).
Then, the feed roller (11) is intermittently driven to convey the wrapping paper (6), and when the conveyance is stopped, a sachet is formed by vertical heat sealing and a tablet is put into the sachet by opening the shutter (3). Each operation of sealing the sachet by lateral heat sealing is performed.

FIG. 3 shows a control device for the tablet packing machine according to the present invention, in which (13) is a control device on the operating device (10) side, and (1)
Reference numeral 4) is a control device on the side of the packaging machine (11), which is connected by a transmission line (17) through interfaces (15) and (16) for converting transmission data to serial and receiving data to parallel. The control device (13) includes a central processing unit (18), a system memory (19) in which a control procedure on the operating device (10) side is programmed, and a key input unit (1).
2) A keyboard interface (20) that detects the operation of the touch panel and generates a key input signal, a controller (21) that controls the display of a CRT (22), and drug file memories M11 to M1n and prescriptions corresponding to each drug type. Data memories M21 to M2n, control data memory M3, register R3
It is equipped with R4. Then, the control device (14) has a system memory (25) programmed with a control procedure on the packaging machine (11) side, a packaging machine controller (28) for controlling the packaging operation of the packaging machine (11), and a central processing unit ( 24)
, A memory M4, a control counter (27), and registers R1 and R2.

FIG. 4 is a flow chart showing the operation when the control device (13) registers the names, abbreviation codes and code numbers of all the medicines handled by the pharmacy in the medicine file memories M11 to M1n. The process is started by operating the function key indicating the start of registration. N0
In the step, an arbitrary code number for the chemical species is input by operating the ten keys of the key input unit (12). At this time, the medicine to be registered can be packed in the packing machine (11),
If any of the tablet cases (5) ... (5) is filled, a code number other than “0” is entered with the numeric keypad, and powder or water that cannot be packaged by the packaging machine (11). In the case of a drug, "0" is input by the ten keys.
The N1 step is to store the code number data input by the key in the medicine file memories M11 to M1n. The drug file memories M11 to M1n corresponding to each drug type have storage areas m7, m8, m9, and m10 as shown in FIG. 5, and the code number data for each drug is stored in the storage area m7. When the abbreviation for the medicine type is keyed in at the N2 step, it is judged at the N3 step whether or not this abbreviation overlaps with the abbreviations of other already registered medicines, and if not, at the N4 step. The abbreviation code is stored in the storage area m8 of the corresponding storage units M11 to M1n. For example, if "A" is input as an abbreviation for a drug named "A lock", a character code representing the character "A" is stored in the storage area m8. On the other hand, when the codes are duplicated, the process is changed from the N3 step to the N2 step and waits until the code is re-keyed. Then, when the medicine name of the medicine type is keyed in in the N5 step, each character constituting the medicine name is stored in the storage area m9 by the character code in the N6 step. This process is repeated for each drug type, and the drug file memory M11-
The code number data, the abbreviation code and the medicine name are registered in M1n, and when it is detected in step N7 that the function key indicating the end of registration of the key input section (12) is operated, the registration operation is ended.

The control device (14) performs packaging control based on the control data transmitted from the control device (13), and the transfer mode between the control devices (13) and (14) is the control device (1).
4) starts by transmitting a transfer request signal to the control device (13). At this time, the control device (14) periodically outputs the transfer request signal in a state where the packaging control is not performed. FIG. 6 is a flow chart showing a normal operation of the control device (13), and the processing based on this flow chart is always executed except for the registration operation to the medicine file memories M11 to M1n. In the N10 step, "1" is stored in the register R3 and the transfer number is set to 1, and "0" is stored in the register R4. In the N11 step, the presence or absence of the transfer request signal from the control unit (14) is checked. If the transfer request signal is not output, the presence / absence of a key input is determined in step N12. When the key input section (12) is operated,
When the abbreviation of the medicine to be administered and the number of medicines and the number of days to be taken are keyed in every morning, noon, evening and before going to bed, in step N13, prescription data is created based on this key input according to the format of FIG. Any prescription data memory M21
~ M2n, but hereinafter stored in the prescription data memory M21.

FIG. 8 is a flow chart for explaining the operation at N13 step. When the abbreviation of the medicine is keyed in at the n0 step, the medicine file memory M1 at the n1 step.
1 to M1n are indexed to determine which chemical has been keyed in, and the n2 step is performed. However, if the same abbreviation as the key input is not stored in any of the medicine file memories M11 to M1n, the process returns to the n0 step and waits for another abbreviation input. In the n2 step, the code number and the medicine name of the medicine corresponding to the keyed abbreviation are read from the medicine file memories M11 to M1n and stored in the storage areas m5 and m6 of the prescription data memory M21, respectively. Then, in the n3 step, the number of medicines for each of the morning, noon, evening, and before bedtime is input, and in the n4 step, the morning number is input to each address 0 to 3 in the storage area m2 of the prescription data memory M21.
When the drug number data for each day, evening, and bedtime is written and there is a key input in the n5 step, it is determined in the n6 step whether the content of the key input is an abbreviation for a drug or the number of doses. When a plurality of types of tablets are packed in one package, the abbreviation is input again. Therefore, the process returns to the n1 step and the same process is repeated, and the medicines matching this abbreviation are stored in the prescription data memory M21. The code number, drug name, and number of drugs are stored. When the medicines to be packed in one packet and the number of medicines have been set, and the number of days to take the medicine is entered in n5 steps, the steps from n6 to n7 are carried out to the storage area m1 of the prescription data memory M21. Store days data. In the n8 step, the day
The total number of packets for each day, evening and before going to bed is calculated and stored in each address 0 to 3 of the storage area m3 of the prescription data memory M21. In the n9 step, the transfer number stored in the register R3 is written in the storage area m4 of the prescription data memory M21, the content of the register R3 is incremented by 1 in the n10 step, the transfer number is incremented by 1, and the N11 step is performed. . When the prescription data is again keyed in the state where the transfer request signal is not transmitted, the prescription data is stored in the memory M22. At this time, the content of the register R3 is incremented by 1 in the storage area m4 of the prescription data memory M22. Because of being
The forwarded transfer number is stored.

FIG. 9 shows a CRT at the time of such key input.
The display contents of (22) are shown, and the name of the drug designated by the operator's key input and the number and the number of days of this drug every morning, noon, evening and before bedtime are displayed (31) (32) ( 33)
And the code numbers read from the medicine file memories M11 to M1n based on the abbreviations are displayed on the display unit (34). In the input example shown in FIG. 9, one A tablet, one B tablet, and one C tablet are packed every morning, noon, and evening for 7 days.
It indicates that the key input was to pack one unit of E powder for 7 days each in the evening and before bed. E is a powder
The powder cannot be packaged in the packaging machine (11) and is packaged by another packaging machine dedicated to powder medicine or manually, but is input for inventory management. Therefore, the prescription data memory M21
No. 1 to No. In each storage area m5 up to 4, the code number data of each chemical of A, B, C, E is written, respectively, and No. 1 to No. The drug number data "1" is written to the addresses 0 to 2 corresponding to morning, noon, evening, and before going to bed of each storage area m2 for storing the drug number data up to 3, and "0" is written to the address 3. Is written, and No. "1" is written in each address 0 to 3 of the storage area m2 of 4, and the number of days data "7" is written in the storage area m1.
And by inputting the drug number data and the number of days data, morning, noon,
The total number of packets for each evening and before going to bed is calculated and stored in each address 0 to 3 of the storage area m3, and the CRT (22)
Is displayed on the display section (35). Moreover, since the E powder cannot be packaged in the packaging machine (11), the code number is "0".
Is stored in the prescription data memory M21.
The display part (34) of (22) displays "..." For E powder to indicate that packaging is not possible.

In this way, the prescription data is created and N11
Returning to the step, when it is detected that the transfer request signal is transmitted from the control device (14), it becomes N14 step and it is judged whether the content of the register R4 is a value other than "0". When the packaging machine (11) is in the packaging operation, the register R4 stores the transfer number of the prescription data which is the basis of the packaging operation at this time. Therefore, at present, the packaging machine (1
When 1) has stopped the packaging operation, the content of the register R4 is "0", so that the process proceeds to the N19 step to judge the presence or absence of prescription data. When the prescription data is stored in the prescription data memory M21 by the process of the above N13 step, the transfer number stored in the storage area m4 of the prescription data memory M21 is written in the register R4 in the N20 step, and the N21 step is performed. The prescription data transferred to the control device (14) is converted into control data according to the format shown in FIG. If any two or more prescription data memories M21 to M2n store the prescription data, the prescription data with the smaller transfer number stored in the storage area m4 is selected.

FIG. 10 shows a flow chart for creating control data. In step n20, memories M21 to M2n storing prescription data are selected, and the selected memory M is selected.
The head storage areas m5 and m2 are designated in the respective storage areas m5 and m2 of 21. In the n21 step, the code number data of the medicine stored in the storage area m5 of the prescription data memory M21 is written in the storage area m5 'of the control data memory M3. The control data memory M3 corresponds to the storage areas m2, m3, m5 of the prescription data memories M21-M2n, and the storage areas m2 ', m3', m.
It has 5 '. In the n22 step, it is judged whether the code number data stored in the storage area m5 'is "0",
If the value is other than "0", the number of steps is n23, and the data on the number of medicines stored in each address 0 to 3 of the storage area m2 of the prescription data memory M21 for each morning, noon, evening and before bedtime is stored in the control data memory. The data is stored in each address 0 to 3 of the storage area m2 'of M3. In the case of "0", "0" is written in each address 0 to 3 of the storage area m2 'of the control data memory M3 in the step n24. The n25 step shifts the storage areas m5 and m2 of the prescription data memory M21 respectively, and the n26 step determines whether or not all the storage areas m5 of the prescription data memory M21 are designated. By repeating the processing from the n21 step to the n26 step, the code number data of the medicine stored in the storage area m5 of the prescription data memory M21 selected in the n20 step is transferred to the control data memory M3 and the code number data is stored. When the value is other than "0", the drug number data of the drug type is directly used as the control data memory M
3 is written, and in the case of "0", the drug number data of the drug type is corrected to "0" and written in the control data memory M3. Therefore, in the input example shown in FIG. 1 to No. 3 in storage area m5 'up to 3
・ C Code number data of each tablet, No. 4 storage areas m
In the 5 ', "0" is written corresponding to the E powder, and the No. of the control data memory M3. 1 to No. "1" is written in the addresses 0 to 2 of each storage area m2 'up to 3 and "0" is written in the address 3, and No. Four
"0" for each address from 0 to 3 in the memory area m2 '
Are written respectively.

In the n27 step, the first address 0 in the storage area m3 of the storage section of the prescription data memory M21 selected in the n20 step is designated, and the address of each of the storage areas m2 'and m3' of the control data memory M3 is specified. 0
Are specified respectively. In the n28 step, it is determined whether the logical sum of the drug number data for each drug type stored in the address 0 of each storage area m2 'is "0". At this time, if at least one of the drug number data stored in the address 0 of each storage area m2 'is other than "0", the total package for the morning stored in the address 0 of the storage area m3 in step n29. The numerical data is written to address 0 of the storage area m3 'of the control data memory M3. If all the drug number data stored in the address 0 of each memory area m2 'is "0", "0" is written in the address 0 of the memory area m3' of the control data memory M3 in step n30. In the n31 step, the address in the storage area m3 of the storage unit of the prescription data memory M2 selected in the n27 step is shifted from 0 to 1 and each storage area m of the control data memory M3 is changed.
All the 2'addresses are shifted from 0 to 1, and in the n32 step, it is determined whether the address of the storage area m3 of the prescription data memory M2 is over, and if the address is within 3, the n
Go to step 28. Then, in the processing from step n28 to step n32, whether the logical sum of the drug number data for each drug type stored in each address 1 of each storage area m2 'of the control data memory M3 is "0" It is determined whether or not the total package number data needs to be corrected, and if it is not "0", the data stored in the address 1 of the storage area m3 is written to the address 1 of the storage area m3 'and "0" In the case of ",""0" is written in the address 1 of the storage area m3 'to correct the total packaging number data. Similarly, the total number of packets for the evening and before going to bed is determined to be corrected by the processing from step n28 to step n32, respectively, and the control data memory M
Predetermined data is written in addresses 2 and 3 of the memory area m3 'of 3, respectively. When the address of the prescription data memory M2 exceeds the storage area m3, the steps n32 to N22
It becomes a step. Therefore, according to the prescription input of this example,
Only E powder is used before bedtime, and control data memory M
Since the logical sum of the data stored in the address 3 of each storage area m2 'in 3 is "0", the storage area m3'
The corrected value "0" is written in the address 3 of.

In step N22, it is determined whether the total number of packets stored in addresses 0 to 3 of the storage area m3 'of the control data memory M3 is "0" for every morning, noon, evening and before going to bed. , "0", the packaging machine (11) does not need to perform packaging, and the process returns to step N11. Then morning, noon,
At least one of the total packages before evening / sleep is "0"
Otherwise, the packaging machine (11) needs to package the control data, and the control data is transferred to the control device (14) in step N23.
It is serial-converted in 5) and transmitted. Then, after the transfer is completed, the process returns to the N11 step, but the control device (14) does not output the transfer request signal because the control of the packaging machine (11) is performed by receiving the control data. Therefore, the control device (13) repeatedly determines the presence / absence of a key input in the N12 step, and when there is a key input, the N13 step is performed, and the key input data is stored in any of the prescription data memories M21 to M2n in which the prescription data is not stored. To do.

The operation of the control device (14) will be described with reference to the flow chart of FIG. When the transfer request signal is output and the control data is received in the N0 'step, the N1' step is changed to the N2 'step and the control data is stored in the memory M4. The memory M4 is a memory area m2 ′ of the memory M3.
・ Memory area corresponding to m3 '・ m5' m2 "・ m3" ・ m
It has 5 ”and stores the data of the number of medicines, the data of the total number of packages, and the code number of the drug type. The N3 ′ step sequentially increments from“ 0 ”to“ 3 ”each time 1 is added. The ternary control counter (27) that repeatedly counts is set to "0".
Set to. In the N4 'step, it is determined whether the content of the storage area m3 "of the memory M4 is" 0 ". The storage area m3 "stores the total number of packages at four addresses 0 to 3 corresponding to morning, noon, evening and before going to bed. In this case, the content CN of the control counter (27) is" Address 0 is designated for "0", and it is determined whether the total package data in the morning is "0". In this example, the number of packets for morning use is 7 days, and the process proceeds to step N5 '. In the N5 'step, the code number data stored in the storage area m5 "of the memory M4 is stored in the register R1 and the drug number data stored in the storage area m2" is stored in the register R2. At this time, as for the storage area m2 ", since the content CN of the control counter (27) is" 0 ", the drug number data stored in the address 0 of the storage area m2" is first read and stored in the register R2. Therefore, register R1 has A and B
・ C The code number data of each tablet is written, and the register R
The data on the number of medicines in the morning for these tablets is written in 2. The N6 'step determines whether the content of the register R2 is "0", but if the drug number data of at least one tablet type for each of A, B, and C tablet types is other than "0", it becomes the N7' step. And the tablet is removed. N
In the 7'step, the code number data for the tablet type having the drug number data other than "0" is read from the register R1 and introduced into the packaging machine controller (28). Then, the packaging machine controller (28) outputs an extraction signal to the tablet cases (5) ... (5) accommodating various tablets of A, B and C. Therefore, the tablet cases (5) ... (5) to which the extraction signal is introduced are driven to extract one tablet. In the N8 'step, "1" is subtracted from the drug number data of the tablet type for which the extracting operation has been performed, and the process returns to the N6' step. In this example, the number data of each drug of A, B, and C stored in the register R2 in order to package each tablet of each drug of A, B, and C in the morning sachet is "0". Become. Therefore, the tablets for one minute in the morning are extracted and introduced into the hopper (2), and the packing operation is performed in the next N9 'step. At step N9 ', the packaging machine controller (28) gives control signals to the shutter (3), the horizontal heat seal mechanism (10), and the vertical heat seal mechanism (9), respectively, to insert tablets, seal the sachets, and form sachets. Then, a control signal is given to the drive device of the feed roller (11) to move the wrapping paper (6) by a predetermined dimension in the longitudinal direction, and the packaging operation for the sachets for the morning dose is completed. N10 '
The step specifies the address 0 of the storage area m3 "of the memory M4 by the content" 0 "of the control counter (27), subtracts" 1 "from the data stored therein, and N11 '.
In the step, it is judged whether the data of all addresses 0 to 3 in the storage area m3 "is" 0 ". in this case,
This is the stage when "1" is subtracted from the data at address 0 in the storage area m3 "after one package for the morning dose is completed. N12 '
At the step, the content CN of the control counter (27) is advanced from "0" to "1" to return to the N4 'step. And N
In the 4'step, since the content of the control counter (27) is "1", the address 1 of m3 "is designated and it is determined whether the content is" 0 ". At this time, the content of the address 1 is" 7 ". Therefore, the process shifts to N5 'step and the packing operation for lunch is started.

In the N5 'step, the code number data stored in the storage area m5 "is stored in the register R1 and the drug number data stored in the address 1 of each storage area m2" is stored in the register R2. Then, from the N6 'step to the N7' step, tablets are extracted from the tablet cases (5) ... (5) for tablet types in which the drug number data stored in the register R2 is other than "0",
In the N8 'step, "1" is obtained from the drug number data in the register R2.
Subtract. In the present example, since the sachets for lunch are also packaged one by one for each of the drugs A, B and C, the drug number data in the register R2 is all "0" and the steps N6 'to N9'. In the N9 'step, the packing operation of the one-minute packet for lunch taken out into the hopper (2) is performed, and N1
In the 0'step, "1" is subtracted from the data stored in the address 1 of the storage area m3 "to store the end of the daytime one-pack operation. Then, from the N11 'step to the N12' step, the content CN of the control counter (27) is advanced from "1" to "2". Therefore, the next N
From step 4 ', since the content of the control counter (27) is "2", the storage area m5 "/ m2" is designated as the address 2 and the processing for the evening one-pack operation is performed. When the processing for the package is completed, the content CN of the control counter (27) is advanced from "2" to "3" and N4 '.
Return to step. At this time, the content of the address 3 of the storage area m3 "is" 0 ", and the steps N4 'to N11'
It becomes a step. That is, in the input prescription of this example, since the E powder which cannot be packaged by the packaging machine (11) is packaged before bedtime, the packaging operation for the dose before bedtime is omitted. Then, in the N12 'step, the control counter (2
The content of 7) is advanced from "3" to "0", and the process for the morning sachet is performed again. In this way, the packaging operation is repeated in the order of morning, noon and evening until all the data stored in the addresses 0 to 3 of the memory area m3 'of the memory M4 becomes "0". Then, when the packaging of 7-minute packages for 7 days of morning, noon, and evening is completed, it is determined that the packaging for one input prescription is completed, and the process returns from the N11 'step to the N0' step. Then, in the N0 'step, a transfer request signal of prescription data relating to the next packaging operation is transmitted to the control device (13).

When the controller (13) detects that the controller (14) is outputting the transfer request signal at step N11, the prescription data at this time is the controller (14).
Since the transfer number is transferred to the register R4 and the transfer number is stored in the register R4, the steps from N14 to N15. In the N15 step, the corresponding drug file memories M11 to M1n are indexed from the drug names stored in the prescription data memory M21,
In step N16, the cumulative drug number is recorded in the drug number storage area m10 of the memory. In step N17, prescription data memory M21
Is cleared, and in the N18 step, the register R4 is set to "0" to become the N19 step. In this way the control device (13)
Determines that the packaging operation based on the transferred control data is completed based on the presence or absence of the transfer request signal in the N11 step and the contents of the register R4 in the N14 step, the drug type indicated in the prescription data after the packaging is completed. Specify the medicine file memory M11-M1n corresponding to
The drug number data of the drug type is added to the cumulative drug number stored in. When the prescription data is stored in any of the prescription data memories M22 to M2n, the control data is created again, and in the case of a drug type that can be packaged by the packaging machine (11), the control data is stored in the control device (14). Transfer to. Further, the data stored in the medicine file memories M11 to M1n is operated by operating a predetermined key of the key input unit (12) and inputting a display command for instructing display of the data into the central processing unit (18), It is displayed on the CRT (22). That is, in the flowchart of FIG. 6, it is indicated that the display command is generated in the state where the transfer request signal is not transmitted from the control device (14) and the prescription is not input to the key input unit (12) in step N24. When detected by
In the N25 step, the data stored in the drug file memories M11 to M1n is introduced into the CRT controller (21), and the CRT (22) displays the code number, abbreviation code, drug name, and cumulative drug number for each drug type. indicate.

On the display screen of the CRT (22), all the drug species to be dispensed are displayed, and a mark indicating that the drug cannot be packed in the packing machine (11), for example, "..." An identification symbol is added to inform the operator that some prescription information cannot be packaged. In addition, by attaching identification symbols to the types of chemicals that cannot be packed, the packaging machine (1
In 1), during the packaging of the prescription information, the chemical species that cannot be packaged by this packaging machine can be packaged separately.

[0022]

As described above, according to the present invention, a means for storing a registered drug type and packaging availability information of this drug type, and a drug to be dispensed from among the drug types stored in this storage means. A means for extracting the species and inputting the number of medicines of this medicine type, a means for discriminating the medicine species that cannot be packed in the packaging machine based on the medicine packaging availability information, and displaying the extracted medicine species to be administered And a mark is attached to a chemical species that cannot be packed among the chemical species displayed on the display means, and the chemical species and the packaging that can be packaged by the pharmaceutical packaging machine displayed on the same screen of the display means are included. It is possible to identify the chemical species that cannot be packaged, notify the operator of the chemical species that cannot be packaged, and the chemical species that cannot be packaged by the pharmaceutical packaging machine can be separately packaged during packaging by this packaging machine, and the packaging work can be shortened. be able to.

[Brief description of drawings]

FIG. 1 is an external view of a drug packaging machine according to the present invention.

FIG. 2 is a configuration diagram of a medicine packaging machine of the present invention.

FIG. 3 is a configuration diagram of a control device of the present invention.

FIG. 4 is a flow chart showing a registration operation in the medicine file memories M11 to M1n.

FIG. 5 is a diagram showing a storage format of drug file memories M11 to M1n.

FIG. 6 is a flowchart showing the operation of the control device (13).

FIG. 7 is a diagram showing a format of prescription data.

FIG. 8 is a flowchart showing a prescription data creation process.

FIG. 9 is a diagram showing an input example of one prescription.

FIG. 10 is a flowchart showing a control data creation process.

FIG. 11 is a diagram showing a storage format of a control data memory M3.

FIG. 12 is a flowchart showing the operation of the control device (14).

[Explanation of symbols]

 (10) Controller (11) Packaging machine (12) Key input section (13) (14) Control device M11 to M1n Drug file memory M21 to M2n Prescription data memory M3 Control data memory

Claims (1)

[Claims] 1. A means for storing a drug type to be registered and packaging propriety information of this drug type, a drug type to be administered is extracted from the drug types stored in this storage means, and a drug of this drug type is extracted. The display means includes means for inputting a number, means for determining a medicine type that cannot be packaged in the packaging machine based on the medicine packaging availability information, and means for displaying the extracted medicine type to be administered. A control device for a medicine packaging machine, which marks a medicine type that cannot be packed among the displayed medicine types.