CN115510049B - Method, device and equipment for inputting standard data of medicine and storage medium - Google Patents
Method, device and equipment for inputting standard data of medicine and storage medium Download PDFInfo
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- CN115510049B CN115510049B CN202211420665.9A CN202211420665A CN115510049B CN 115510049 B CN115510049 B CN 115510049B CN 202211420665 A CN202211420665 A CN 202211420665A CN 115510049 B CN115510049 B CN 115510049B
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Abstract
The embodiment of the specification provides a method, a device, equipment and a storage medium for inputting standard data of a medicine. The method comprises the following steps: receiving an initial standard data entry application of a medicine; wherein, the initial standard data entry application is accompanied with initial drug data applied as standard data; the label data is used to characterize the drug; acquiring historical transaction data of the medicine; wherein the historical transaction data comprises drug verification data of the drug; and verifying the initial drug data through the drug verification data, and if the initial drug data accords with a preset verification standard, inputting the initial drug data serving as standard data into a standard database. The embodiment of the specification can improve the speed of inputting the data of the standard product.
Description
Technical Field
Embodiments in the present specification relate to the field of databases, and in particular, to a method, an apparatus, a device, and a storage medium for inputting standard product data of a drug.
Background
The standard drug database may store drug information, which may be used as a benchmark. The management of the drug information can be realized by establishing a standard drug database. For example, a drug sales platform can unify drug information by establishing a standard drug database, thereby reducing the occurrence of errors.
At present, when a standard medicine database is established, an operator needs to enter medicine information, and the entry of the medicine information is completed after the audit. However, in the prior art, when inputting the drug information into the standard drug database, manual verification needs to be performed on the input drug information, and the input of the drug information is completed after checking the input drug information without errors.
Therefore, the technical problem that the recording speed is slow when the medicine information is recorded into the database exists in the prior art.
Disclosure of Invention
In view of the above, embodiments of the present disclosure are directed to providing a method, an apparatus, a device and a storage medium for inputting standard data of a medicine, so as to increase the speed of inputting the standard data to some extent.
One embodiment of the present specification provides a method for inputting standard data of a medicine, including: receiving an initial standard data entry application of a medicine; wherein, the initial standard data entry application is accompanied with initial drug data applied as standard data; the standard data is used for characterizing the drug; acquiring historical transaction data of the medicine; wherein the historical transaction data comprises drug verification data of the drug; and checking the initial medicine data through the medicine checking data, and if the initial medicine data accords with a preset checking standard, inputting the initial medicine data serving as standard data into a standard database.
One embodiment of the present specification provides a drug product data entry device including: the receiving module is used for receiving an initial standard data entry application of the medicine; wherein, the initial standard data entry application is accompanied with initial drug data applied as standard data; the label data is used to characterize the drug; the acquisition module is used for acquiring historical transaction data of the medicine; wherein the historical transaction data comprises drug verification data of the drug; and the processing module is used for verifying the initial medicine data through the medicine verification data, and if the initial medicine data meets a preset verification standard, the initial medicine data is used as standard data to be recorded into a standard database.
The present specification provides a computer device, which includes a memory and a processor, wherein the memory stores a computer program, and the processor implements the method of any one of the above embodiments when executing the computer program.
The embodiment of the present specification provides a computer readable storage medium, on which a computer program is stored, and the computer program is executed by a processor to implement the method of any one of the above embodiments.
In a plurality of embodiments provided in this specification, an initial standard product data entry application accompanied by initial drug data applied as standard product data is received, historical transaction data including drug verification data is acquired, the initial drug data is verified by the drug verification data, and the initial drug data is entered into a standard product database as standard product data when the initial drug data meets a preset verification standard. The method can improve the speed of inputting the data of the standard products.
Drawings
Fig. 1 is a schematic diagram of an application scenario example of a standard product data entry method provided in an embodiment of the present specification.
Fig. 2 is a schematic diagram of an application scenario example of the standard data entry method provided in one embodiment of the present specification.
Fig. 3 is a schematic diagram of a flow of a method for inputting standard data provided in an embodiment of the present specification.
Fig. 4 is a schematic diagram of a standard data entry device provided in one embodiment of the present description.
FIG. 5 is a schematic diagram of a computer device according to one embodiment of the present disclosure.
Detailed Description
SUMMARY
In the related art, when a standard product database of a medicine is established, an operator needs to enter medicine information, and after the medicine information is audited, the entry of the medicine information is completed, so that the standard product data of the medicine is established. However, in the prior art, when inputting the medicine information into the standard product database, an operator or a background auditor needs to manually audit the input medicine information, and after checking that the input medicine information is correct, the input medicine information is completed. Because the manual auditing speed is low and no standard auditing standard exists, the problems of low entry speed and low entry efficiency of the standard product data of the medicine caused by low auditing speed exist when the medicine information is entered into the standard product database.
Therefore, it is necessary to provide a method for inputting standard product data of a drug, which can automatically check the received drug data, and input the drug data as standard product data into a standard product database when the check is passed. The technical problems of low input speed and low input efficiency when the medicine data are input into the standard product database are solved.
Example of a scene
Referring to fig. 1 and fig. 2, an example of an application scenario of a drug sample data entry system is provided in this specification. The standard data entry system may include a server interacting with a standard database and a plurality of clients interacting with the server. The client can acquire initial drug data of the drug, generate an initial standard product data entry application attached with the initial drug data according to the acquired initial drug data of the drug, and send the initial standard product data entry application to the server. The server can receive an initial standard product data entry application sent by the client, obtain initial medicine data of the medicine, and can obtain historical transaction data of the medicine, wherein the historical transaction data comprises medicine verification data of the medicine, verify the initial medicine data according to the medicine verification data in the historical transaction data, and enter the initial medicine data serving as the standard product data into a standard product database under the condition that the initial medicine data meets a preset verification standard.
In this scenario embodiment, the client may obtain initial drug data of the drug by scanning a tracing code or a commodity barcode set on a packaging box of the drug. Specifically, referring to table 1, the initial drug data may include drug basic information of the drug. The basic information of the drug may include a commodity code of the drug, a common name of the drug, a specification of the drug, a manufacturer of the drug, an approval letter of the drug, a type of the drug, a basic unit of the drug, a formulation of the drug, a business category of the drug, and the like. After the client acquires the initial drug data, the client can send an initial standard product data entry application with the initial drug data attached to the server.
TABLE 1
For example, after the initial drug data of the drug is acquired, a corresponding standard product code may be set for the initial drug data, so that the initial drug data corresponding to the standard product code may be queried according to the standard product code.
The server may verify the initial drug data in the received initial standard data entry application. Specifically, the server may obtain historical transaction data for the drug. Wherein the historical transaction data for the drug may include drug verification data for the drug. The drug verification data may include drug substance information for the drug,
the server can check the initial drug data through the drug check data, and if the initial drug data accords with the preset check standard, the initial drug data can be used as the standard data to be recorded into the standard database. Specifically, the preset calibration standard may be: and under the condition that the basic information of the medicines corresponding to the initial medicine data is the same as the basic information of the medicines corresponding to the medicine verification data, confirming that the initial medicine data accords with the preset verification standard. The historical transaction data of the medicine may refer to transaction record data generated during circulation of purchasing or selling the medicine.
Specifically, the historical transaction data of the medicine may be stored in the server, or may be stored in another server connected to the server through a network.
Further, the preset calibration standard may also be: and confirming that the initial medicine data accords with the preset verification standard under the condition that the basic medicine information corresponding to the initial medicine data is the same as the basic medicine information corresponding to the medicine verification data and the historical transaction data accords with the set conditions.
Specifically, the historical transaction data may also include transaction times for the drug. The transaction times of the medicines can refer to the purchase times, the sale times and the like of the medicines corresponding to the medicine verification data. When the initial drug data is verified through the drug verification data, the initial drug data can be further verified according to the transaction times of the drugs on the basis of determining whether the initial drug data is the same as the drug verification data, so that the reasonability of the initial drug data in the verification process can be improved. For example, the set condition may be that the set condition is greater than a preset transaction time threshold, on the basis that the initial drug data is the same as the drug verification data, it is determined whether the transaction time of the drug corresponding to the drug verification data is greater than the preset transaction time threshold, and if the transaction time of the drug corresponding to the drug verification data is greater than the preset transaction time threshold, the initial drug data may be used as the standard product data, and the initial drug data is entered into the standard product database. For example, the preset transaction frequency threshold may be 5, and under the condition that the initial drug data is the same as the drug verification data, if the transaction frequency of the drug corresponding to the drug verification data is greater than 5, it may be determined that the drug verification data meets the set condition, and the initial drug data may be entered into the standard product database as the standard product data.
In particular, the historical transaction data may also include the number of pharmacy associated with the drug verification data. The number of pharmacy associated with the drug corresponding to the drug verification data may refer to the number of pharmacy that generated the drug verification data. That is, the number of drug stores that purchase or sell the drugs corresponding to the drug verification data. As an example, the drug verification data may be obtained by a pharmacy purchasing or selling drugs, and the number of the pharmacy associated with the drug corresponding to the drug verification data is 1. The medicine verification data may be obtained by purchasing or selling medicines from a plurality of pharmacy, for example, may be obtained by purchasing or selling medicines from 3 pharmacy, and in this case, the number of pharmacy related to the medicine corresponding to the medicine verification data is 3. Therefore, when the initial drug data is verified through the drug verification data, the initial drug data can be verified according to the number of the drug stores associated with the drug corresponding to the drug verification data on the basis of determining whether the initial drug data is the same as the drug verification data, and therefore reasonability in the verification process of the initial drug data is further improved. For example, the setting condition may be that the setting condition is greater than a preset associated pharmacy quantity threshold, on the basis that the initial drug data is the same as the drug verification data, it is determined whether the associated pharmacy quantity of the drug corresponding to the drug verification data is greater than the preset associated pharmacy quantity threshold, and if the associated pharmacy quantity of the drug corresponding to the drug verification data is greater than the preset associated pharmacy quantity threshold, the initial drug data may be used as the standard product data, and the initial drug data may be entered into the standard product database. For example, the preset threshold of the number of associated pharmacy stores may be 2, and under the condition that the initial drug data is the same as the drug verification data, if the number of associated pharmacy stores of the drug corresponding to the drug verification data is greater than 2, it may be determined that the drug verification data meets the set condition, and the initial drug data is entered into the standard database as the standard data.
Furthermore, the server can record and apply for the initial standard data to be added into a waiting state task set under the condition that the drug verification data in the historical transaction data do not accord with the set conditions; the waiting state task set can comprise at least one standard data entry application, and historical transaction data corresponding to the standard data entry application do not accord with set conditions. The server can poll and read the standard product data entry application in the waiting state task set so as to take the initial drug data attached to the standard product data entry application as the standard product data to be entered into the standard product database under the condition that the historical transaction data corresponding to the standard product data entry application meets the set conditions. For example, under the condition that the initial drug data and the drug verification data are the same, when the set conditions are that the transaction frequency of the drug corresponding to the drug verification data is greater than 5 and the number of the associated pharmacy of the drug corresponding to the drug verification data is greater than 2, if the transaction frequency of the drug corresponding to the drug verification data and the number of the associated pharmacy are 5 and 2 respectively, the set conditions are not met, then the initial standard data with the initial drug data may be entered and applied to be added to the waiting status task set. Due to the fact that purchase and sale of medicines can cause changes of the transaction times of the medicines corresponding to the medicine verification data in the historical transaction data of the medicines and the number of the associated drug stores, and further the medicine verification data in the historical transaction data can meet set conditions, the standard data entry application in the waiting state task set can be polled and read, and under the condition that the medicine verification data in the historical transaction data corresponding to the standard data entry application meet the set conditions, initial medicine data of the standard data entry application are taken as the standard data to be entered into a standard database.
Further, the initial drug data attached to the initial standard product data entry application may be the same as the historical drug data attached to the historical standard product data entry application in the waiting state task set, and therefore, before the initial drug data of the initial standard product data entry application is entered into the standard product database as the standard product data or before the initial standard product data entry application is added to the waiting state task set, the historical standard product data entry application may be obtained from the waiting state task set, and in the case that the historical drug data is the same as the initial drug data, the initial standard product data entry application and the historical standard product data entry application are merged.
System architecture
The embodiment of the specification provides a standard data entry system. The standard data entry system may include a plurality of clients and servers. The client may be an electronic device with network access capabilities. Specifically, for example, the client may be a desktop computer, a tablet computer, a notebook computer, a smart phone, a digital assistant, a smart wearable device, a shopping guide terminal, a television, a smart speaker, a microphone, and the like. Wherein, wearable equipment of intelligence includes but not limited to intelligent bracelet, intelligent wrist-watch, intelligent glasses, intelligent helmet, intelligent necklace etc.. Alternatively, the client may be software capable of running in the electronic device.
The server may be an electronic device having a certain arithmetic processing capability. Which may have a network communication module, a processor, memory, etc. Of course, the server may also refer to software running in the electronic device. The server may also be a distributed server, which may be a system with multiple processors, memory, network communication modules, etc. operating in coordination. Alternatively, the server may also be a server cluster formed by several servers. Or, with the development of scientific technology, the server can also be a new technical means capable of realizing the corresponding functions of the specification implementation mode. For example, it may be a new form of "server" implemented based on quantum computing.
Example methods
Referring to fig. 3, one embodiment of the present disclosure provides a method for inputting standard data. The standard data entry method can be applied to a server. The method of standard data entry may include the following steps.
Step S110: receiving an initial standard data entry application of a medicine; wherein, the initial standard data entry application is accompanied with initial drug data applied as standard data; the label data is used to characterize the drug.
In some cases, the client may send an initial label data entry application to the server to request the server to enter initial drug data, accompanied by the initial label data entry application, into the label database as label data.
In this embodiment, the server may receive the initial standard product data entry application sent by the client, and obtain initial drug data attached to the initial standard product data entry application.
The initial standard data entry application may be sent by the client when the client acquires initial drug data of the drug. The initial drug data may include drug basic information of the drug, among others. Specifically, the client can obtain initial drug data of the drug by scanning a drug tracing code or a commodity bar code arranged on a packaging box of the drug. After the client acquires the initial drug data of the drug, an initial standard product data entry application with the initial drug data of the drug can be sent to the server. For example, the medicine tracing code or the commodity barcode provided on the packing box of the medicine may be scanned by a scanning method such as laser scanning, infrared scanning, or image scanning. Thus, the client can automatically acquire the initial drug data of the drug.
Further, the initial drug data may further include a label code of the drug, and the label code of the drug may be used to identify the initial drug data, so that after the initial drug data is entered into a label database as label data, the corresponding label data may be queried through the label code.
The standard database may refer to a database for storing standard data of medicines. The standard product data can be standardized and normalized medicine data, one medicine corresponds to one unique standard product data, and the standard product data is stored in the standard product database without being repeated.
Step S120: acquiring historical transaction data of the medicine; wherein the historical transaction data comprises drug verification data of the drug.
In some cases, after initial drug data is obtained based on the initial standard data entry application, the initial drug data needs to be verified, so that the initial drug data can be entered into the standard database as the standard data under the condition that the initial drug data meets the preset verification standard.
In this embodiment, the server may obtain historical transaction data including the drug, wherein the historical transaction data of the drug may include drug verification data of the drug, such that the initial drug data may be verified based on the drug verification data of the drug. The drug verification data in the historical transaction data can refer to transaction record data generated in the circulation process of purchasing, selling and the like of the drug. The drug verification data may include basic information of the drug, and the basic information of the drug may include a commodity code of the drug, a common name of the drug, a specification of the drug, a manufacturer of the drug, an approval document number of the drug, a type of the drug, a basic unit of the drug, a dosage form of the drug, a business category of the drug, and the like.
Step S130: and checking the initial medicine data through the medicine checking data, and if the initial medicine data accords with a preset checking standard, inputting the initial medicine data serving as standard data into a standard database.
In some cases, after the historical transaction data for the drug is obtained, the initial drug data may be verified according to drug verification data in the historical transaction data.
In this embodiment, when the initial drug data is verified according to the drug verification data of the historical transaction data, the verification of the initial drug data may be performed by determining whether the initial drug data and the drug verification data are the same, and when the initial drug data is the same as the drug verification data, it is determined that the initial drug data verification meets the preset verification standard. Specifically, when determining whether the initial drug data and the drug verification data are the same, the determination may be performed by determining whether the drug basic information corresponding to the initial drug data and the drug basic information corresponding to the drug verification data are the same, and when the drug basic information corresponding to the initial drug data and the drug basic information corresponding to the drug verification data are the same, determining that the initial drug data meets the preset verification standard.
In this embodiment, in order to improve the accuracy when verifying the initial drug data, the initial drug data may be further verified according to a set condition, where the set condition may be set according to an actual situation of the drug, on the basis of verifying the initial drug data according to whether the basic drug information corresponding to the initial drug data is the same as the basic drug information corresponding to the drug verification data in the historical transaction data. Specifically, it may be further determined whether the drug verification data in the historical transaction data meets the set condition under the condition that the drug basic information corresponding to the initial drug data is the same as the drug basic information corresponding to the drug verification data. And under the condition that the drug verification data meet the set conditions, inputting the initial drug data serving as the standard product data into the standard product database.
In some embodiments, the historical transaction data may further include transaction times of a drug corresponding to the drug verification data. In the case that the initial drug data is the same as the drug verification data, entering the initial drug data as standard data into a standard database may include: and under the condition that the basic information of the medicines corresponding to the initial medicine data is the same as the basic information of the medicines corresponding to the medicine verification data, and the transaction times of the medicines corresponding to the medicine verification data are larger than a preset transaction time threshold value, taking the initial medicine data as the standard data to be recorded into a standard database.
In some cases, the drug verification data in the historical transaction data for the drug may be stored uniquely, i.e., the same drug data as the drug verification data does not exist in the historical transaction data. The historical transaction data may also include transaction times of the drugs corresponding to the drug verification data. In order to improve the reasonability and accuracy in the process of checking the initial medicine data, when the initial medicine data are checked, the set conditions can be determined according to the transaction times of the medicines corresponding to the medicine checking data.
In this embodiment, specifically, for example, the transaction frequency of the medicine corresponding to the medicine verification data included in the historical transaction data may be the purchase frequency, the sale frequency, or the like of the medicine corresponding to the medicine verification data in the process of circulation, and may be 1 or more times. The setting conditions may be: greater than a preset transaction number threshold. In the process of checking the initial drug data, whether the transaction times of the drugs corresponding to the initial drug data meet set conditions or not can be judged on the basis that the drug basic information corresponding to the initial drug data is the same as the drug basic information corresponding to the drug checking data, namely whether the transaction times of the drugs corresponding to the drug checking data are larger than a preset transaction time threshold value or not, if the transaction times of the drugs corresponding to the drug checking data are larger than the preset transaction time threshold value, the initial drug data can be used as the standard data, and the initial drug data are recorded into a standard database. For example, the preset transaction number threshold may be 5, and under the condition that the initial drug data is the same as the drug verification data, if the transaction number of the drug corresponding to the drug verification data is greater than 5, it may be determined that the transaction number of the drug corresponding to the drug verification data meets the set condition, and the initial drug data may be entered into the standard product database as the standard product data.
In some embodiments, the historical transaction data further includes an associated pharmacy quantity of the drug to which the drug verification data corresponds. In the case that the initial drug data is the same as the drug verification data, entering the initial drug data as standard data into a standard database may include: and under the condition that the basic information of the medicines corresponding to the initial medicine data is the same as the basic information of the medicines corresponding to the medicine verification data, and the number of the associated pharmacy of the medicines corresponding to the medicine verification data is greater than a preset threshold value of the number of the associated pharmacy, taking the initial medicine data as the standard data and inputting the standard data into a standard database.
In some cases, the drug verification data in the historical transaction data may be associated with multiple drug stores, i.e., the drug corresponding to the drug verification data has been purchased, sold, etc. at the multiple drug stores. In order to improve the reasonableness and accuracy in the process of checking the initial medicine data, when the initial medicine data is checked, the setting conditions can be determined according to the number of the pharmacy related to the medicine checking data.
In this embodiment, the number of drug stores related to the drug verification data may be the number of drug stores that generate the drug verification data, for example, the drug verification data may be obtained by purchasing or selling drugs in one drug store, in this case, the number of drug stores related to the drug verification data is 1, the drug verification data may be obtained by purchasing or selling drugs in a plurality of drug stores, for example, 3 drug stores may be purchased or sold, and in this case, the number of drug stores related to the drug verification data is 3. The setting conditions may be: greater than a preset associated pharmacy quantity threshold. When the initial drug data is verified, whether the number of the associated pharmacy of the drug verification data is larger than a preset associated pharmacy number threshold value or not can be judged on the basis that the basic drug information corresponding to the initial drug data is the same as the basic drug information corresponding to the drug verification data, if the number of the associated pharmacy of the drug verification data is larger than a second set threshold value, the initial drug data can be used as standard data, and the initial drug data is recorded into a standard database. For example, the preset threshold of the number of associated drug stores may be 2, and in the case that the basic information of the drug corresponding to the initial drug data is the same as the basic information of the drug corresponding to the drug verification data, if the number of the associated drug stores of the drug verification data is greater than 2, it may be determined that the drug verification data meets the set condition, and the initial drug data may be entered into the standard product database as standard product data.
In some embodiments, the historical transaction data for the drug may include a plurality of drug verification data. Wherein at least some of the plurality of drug verification data belong to different drugstores. In the case that the initial drug data is the same as the drug verification data, entering the initial drug data as standard data into a standard database may include: and under the condition that the plurality of medicine verification data are the same and the initial medicine data are the same as the plurality of medicine verification data, taking the initial medicine data as the standard product data to be recorded into a standard product database.
In some cases, during the circulation of the medicine, such as purchasing and selling, each time purchasing or selling is performed, medicine verification data of the medicine is generated. The medicine corresponding to any two pieces of medicine verification data in the plurality of medicine verification data may be generated by purchasing or selling in the same pharmacy, or may be generated by purchasing or selling in different pharmacies. Therefore, determining whether the initial drug data and the drug verification data are the same may refer to determining whether the initial drug data and the multiple drug verification data are the same.
In some embodiments, entering the initial drug data as label data into a label database in the event that the initial drug data is the same as the drug verification data may include: and under the condition that the initial medicine data is the same as the medicine verification data and the historical transaction data meets set conditions, taking the initial medicine data as standard product data to be recorded into a standard product database. The method for inputting the standard data of the medicines can further comprise the following steps: under the condition that the historical transaction data do not accord with the set conditions, inputting and applying the initial standard data to be added into a waiting state task set; the waiting state task set comprises at least one standard data entry application, and historical transaction data corresponding to the standard data entry application do not accord with the set conditions; and polling and reading the standard product data entry application in the waiting state task set so as to take the initial drug data of the standard product data entry application as the standard product data entry standard product database under the condition that the historical transaction data corresponding to the standard product data entry application meets the set conditions.
In the embodiment, the server can record and apply the initial standard data to add into the waiting state task set under the condition that the drug verification data in the historical transaction data does not accord with the set conditions; the waiting state task set can comprise at least one standard data entry application, and historical transaction data corresponding to the standard data entry application do not accord with set conditions. The server can poll and read the standard product data entry application in the waiting state task set so as to take the initial drug data attached to the standard product data entry application as the standard product data to be entered into the standard product database under the condition that the historical transaction data corresponding to the standard product data entry application meets the set conditions. For example, in the case that the initial drug data and the drug verification data are the same, when the set conditions are that the transaction number of the drug verification data is greater than 5 and the number of associated pharmacies of the drug verification data is greater than 2, if the transaction number of the drug verification data and the number of associated pharmacies are 5 and 2, respectively, the set conditions are not satisfied, the initial standard data entry application with the initial drug data may be added to the waiting status task set. Due to the fact that purchase and sale of medicines can cause changes of transaction times and related pharmacy quantity in medicine verification data in historical transaction data of the medicines, and further medicine verification data in the historical transaction data can meet set conditions, and therefore the standard data entry application in a waiting state task set can be polled and read, and under the condition that the medicine verification data in the historical transaction data corresponding to the standard data entry application meet the set conditions, initial medicine data of the standard data entry application are taken as the standard data to be entered into a standard database.
In some embodiments, prior to entering the initial drug data of the initial label data entry application as label data into a label database, the method may further comprise: acquiring historical standard data entry application aiming at the medicine; the historical standard product data is input and applied with historical medicine data applied as standard product data; merging the initial standard data entry application and the historical standard data entry application under the condition that the historical medicine data is the same as the initial medicine data.
In some embodiments, the initial drug data accompanying the initial label data entry application may be the same as the historical drug data accompanying the historical label data entry application in the wait state task set, and thus, prior to entering the initial drug data of the initial label data entry application as label data into the label database or prior to joining the initial label data entry application into the wait state task set, the historical label data entry application may be obtained from the wait state task set, and in the event that the historical drug data is the same as the initial drug data, the initial label data entry application and the historical label data entry application are merged.
Example apparatus, electronic device, storage medium, and software
Referring to fig. 4, a device for inputting data of a drug label is disclosed. The standard data entry device can comprise a receiving module, an obtaining module and a processing module. The receiving module is used for receiving an initial standard data entry application of the medicine; wherein, the initial standard data entry application is accompanied with initial drug data applied as standard data; the label data is used to characterize the drug; the acquisition module is used for acquiring historical transaction data of the medicine; wherein the historical transaction data comprises drug verification data of the drug; and the processing module is used for verifying the initial medicine data through the medicine verification data, and if the initial medicine data meets a preset verification standard, the initial medicine data is used as standard data to be recorded into a standard database.
The specific functions and effects achieved by the standard data entry device can be explained by referring to other embodiments in this specification, and are not described herein again. The various modules in the means for distributing the prescription tasks may be implemented in whole or in part by software, hardware, and combinations thereof. The modules can be embedded in a hardware form or independent from a processor in the computer device, and can also be stored in a memory in the computer device in a software form, so that the processor can call and execute operations corresponding to the modules.
Please refer to fig. 5. In some embodiments, a computer device may be provided, comprising a memory having a computer program stored therein and a processor that, when executing the computer program, implements the method of standard data entry in the embodiments.
Embodiments of the present specification also provide a computer-readable storage medium having a computer program stored thereon, where the computer program is executed by a computer to make the computer execute the method for inputting standard data in any one of the above embodiments.
Embodiments of the present specification also provide a computer program product comprising instructions which, when executed by a computer, cause the computer to perform the method for data entry of a standard product according to any of the above embodiments.
It should be understood that the specific examples are included merely for purposes of illustrating the embodiments of the disclosure and are not intended to limit the scope of the disclosure.
It should be understood that, in the various embodiments of the present specification, the sequence numbers of the processes do not mean the execution sequence, and the execution sequence of the processes should be determined by the functions and the inherent logic, and should not limit the implementation process of the embodiments of the present specification.
It is to be understood that the various embodiments described in the present specification may be implemented individually or in combination, and the embodiments in the present specification are not limited thereto.
Unless otherwise defined, all technical and scientific terms used in the embodiments of the present specification have the same meaning as commonly understood by one of ordinary skill in the art to which the present specification belongs. The terminology used in the description is for the purpose of describing particular embodiments only and is not intended to limit the scope of the description. As used herein, the term "and/or" includes any and all combinations of one or more of the associated listed items. As used in the specification embodiments and the appended claims, the singular forms "a", "an", and "the" are intended to include the plural forms as well, unless the context clearly indicates otherwise.
It is to be understood that the processor of the embodiments of the present description may be an integrated circuit chip having signal processing capabilities. In implementation, the steps of the above method embodiments may be performed by integrated logic circuits of hardware in a processor or by instructions in the form of software. The Processor may be a general purpose Processor, a Digital Signal Processor (DSP), an Application Specific Integrated Circuit (ASIC), an off-the-shelf Programmable Gate Array (FPGA) or other Programmable logic device, discrete Gate or transistor logic device, or discrete hardware components. The various methods, steps, and logic blocks disclosed in the embodiments of the present specification may be implemented or performed. A general purpose processor may be a microprocessor or the processor may be any conventional processor or the like. The steps of the method disclosed in connection with the embodiments of the present specification may be embodied directly in a hardware decoding processor, or in a combination of hardware and software modules in the decoding processor. The software modules may be located in ram, flash, rom, prom, or eprom, registers, etc. as is well known in the art. The storage medium is located in a memory, and a processor reads information in the memory and completes the steps of the method in combination with hardware of the processor.
It will be appreciated that the memory in the implementations of the specification can be either volatile memory or nonvolatile memory, or can include both volatile and nonvolatile memory. The nonvolatile memory may be a Read Only Memory (ROM), a Programmable Read Only Memory (PROM), an Erasable Programmable Read Only Memory (EPROM), an Electrically Erasable Programmable Read Only Memory (EEPROM), or a flash memory. The volatile memory may be Random Access Memory (RAM). It should be noted that the memory of the systems and methods described herein is intended to comprise, without being limited to, these and any other suitable types of memory.
Those of ordinary skill in the art will appreciate that the various illustrative elements and algorithm steps described in connection with the embodiments disclosed herein may be implemented as electronic hardware or combinations of computer software and electronic hardware. Whether such functionality is implemented as hardware or software depends upon the particular application and design constraints imposed on the implementation. Skilled artisans may implement the described functionality in varying ways for each particular application, but such implementation decisions should not be interpreted as causing a departure from the scope of the present specification.
It is clear to those skilled in the art that, for convenience and brevity of description, the specific working processes of the above-described systems, apparatuses and units may refer to the corresponding processes in the foregoing method embodiments, and are not described herein again.
In the several embodiments provided in this specification, it should be understood that the disclosed system, apparatus, and method may be implemented in other ways. For example, the above-described apparatus embodiments are merely illustrative, and for example, the division of the units is merely a logical division, and other divisions may be realized in practice, for example, a plurality of units or components may be combined or integrated into another system, or some features may be omitted, or not executed. In addition, the shown or discussed mutual coupling or direct coupling or communication connection may be an indirect coupling or communication connection through some interfaces, devices or units, and may be in an electrical, mechanical or other form.
The units described as separate parts may or may not be physically separate, and parts displayed as units may or may not be physical units, may be located in one place, or may be distributed on a plurality of network units. Some or all of the units can be selected according to actual needs to achieve the purpose of the embodiment.
In addition, functional units in the embodiments of the present specification may be integrated into one processing unit, or each unit may exist alone physically, or two or more units may be integrated into one unit.
The functions, if implemented in the form of software functional units and sold or used as a stand-alone product, may be stored in a computer readable storage medium. Based on such understanding, the technical solutions of the present specification may be embodied in the form of a software product, which is stored in a storage medium and includes several instructions for causing a computer device (which may be a personal computer, a server, or a network device) to execute all or part of the steps of the method according to the embodiments of the present specification. And the aforementioned storage medium includes: a U disk, a removable hard disk, a Read Only Memory (ROM), a Random Access Memory (RAM), a magnetic disk, an optical disk, or the like.
The above description is only for the specific embodiments of the present disclosure, but the scope of the present disclosure is not limited thereto, and any person skilled in the art can easily conceive of the changes or substitutions within the technical scope disclosed in the present disclosure, and all the changes or substitutions should be covered within the scope of the present disclosure. Therefore, the protection scope of the present invention shall be subject to the protection scope of the claims.
Claims (14)
1. A method for inputting the data of a standard product of a medicine is characterized by comprising the following steps:
receiving an initial standard data entry application of a medicine; wherein, the initial standard data entry application is accompanied with initial drug data applied as standard data; the label data is used to characterize the drug;
acquiring historical transaction data of the medicine; wherein the historical transaction data comprises drug verification data of the drug; wherein the historical transaction data further comprises transaction times of the drug;
the initial drug data are verified through the drug verification data, and if the initial drug data accord with preset verification standards, the initial drug data are recorded into a standard product database as standard product data, and the method comprises the following steps: checking the initial medicine data through the medicine checking data and the transaction times of the medicines, and if the initial medicine data meet a preset checking standard, inputting the initial medicine data serving as standard product data into a standard product database; wherein, the preset calibration standard comprises: the initial medicine data are the same as the medicine verification data of the medicine, and the transaction times of the medicine are larger than a preset transaction time threshold value.
2. The method of claim 1, wherein the historical transaction data includes a plurality of drug verification data for the drug; at least some of the plurality of drug verification data belong to different drugstores;
the preset calibration standard comprises: the plurality of drug verification data are the same, and the initial drug data are the same as the plurality of drug verification data.
3. The method of claim 1, wherein the initial drug data comprises drug basic information for the drug; the drug verification data comprises drug basic information of the drug; the basic information of the medicine at least comprises at least one of the following information: the commodity code of the medicine, the common name of the medicine, the specification of the medicine, the manufacturer of the medicine, the approval code of the medicine, the basic unit of the medicine, the dosage form of the medicine and the operation category of the medicine;
the initial drug data is verified through the drug verification data, if the initial drug data accords with a preset verification standard, the initial drug data is recorded into a standard product database as standard product data, and the method comprises the following steps:
checking the basic information of the medicines corresponding to the initial medicine data through the basic information of the medicines corresponding to the medicine checking data, and if the initial medicine data accords with a preset checking standard, inputting the initial medicine data serving as standard data into a standard database;
wherein, the preset calibration standard comprises: and the basic information of the medicines corresponding to the initial medicine data is the same as the basic information of the medicines corresponding to the medicine verification data.
4. The method of claim 1, wherein the predetermined verification criteria comprises: under the condition that the initial drug data is the same as the drug verification data and the historical transaction data meets set conditions, taking the initial drug data as standard product data to be recorded into a standard product database;
the method further comprises the following steps:
under the condition that the historical transaction data do not accord with the set conditions, inputting the initial standard data into an application and adding the initial standard data into a waiting state task set; the waiting state task set comprises at least one standard data entry application, and historical transaction data corresponding to the standard data entry application do not accord with the set conditions;
and polling and reading the standard product data entry application in the waiting state task set so as to take the initial drug data of the standard product data entry application as the standard product data entry standard product database under the condition that the historical transaction data corresponding to the standard product data entry application meets the set conditions.
5. The method of claim 4, wherein prior to entering the initial drug data of the initial label data entry application as label data into a label database, the method further comprises:
acquiring historical standard data entry application aiming at the medicine; the historical standard product data is input and applied with historical medicine data applied as standard product data;
and under the condition that the historical medicine data is the same as the initial medicine data, combining the initial standard product data entry application and the historical standard product data entry application.
6. A method for inputting the data of a standard product of a medicine is characterized by comprising the following steps:
receiving an initial standard data entry application of a medicine; wherein, the initial standard data entry application is accompanied with initial drug data applied as standard data; the label data is used to characterize the drug;
acquiring historical transaction data of the medicine; wherein the historical transaction data comprises drug verification data of the drug; wherein the historical transaction data comprises an associated pharmacy quantity of the drug;
the initial drug data are verified through the drug verification data, and if the initial drug data accord with preset verification standards, the initial drug data are recorded into a standard product database as standard product data, and the method comprises the following steps: checking the initial medicine data through the medicine checking data and the number of the medicine stores related to the medicines, and if the initial medicine data meets a preset checking standard, inputting the initial medicine data serving as standard data into a standard database; wherein, the preset calibration standard comprises: the initial drug data is the same as drug verification data of the drugs, and the number of associated drug stores of the drugs is larger than a preset threshold value of the number of associated drug stores.
7. The method of claim 6, wherein the historical transaction data includes a plurality of drug verification data for the drug; at least some of the plurality of drug verification data belong to different drugstores;
the preset calibration standard comprises: the plurality of drug verification data are the same, and the initial drug data are the same as the plurality of drug verification data.
8. The method of claim 6, wherein the initial drug data comprises drug basic information for the drug; the drug verification data comprises drug basic information of the drug; the basic information of the medicine at least comprises at least one of the following information: the commodity code of the medicine, the common name of the medicine, the specification of the medicine, the manufacturer of the medicine, the approved code of the medicine, the basic unit of the medicine, the dosage form of the medicine and the operation category of the medicine;
the initial drug data is verified through the drug verification data, if the initial drug data accords with a preset verification standard, the initial drug data is recorded into a standard product database as standard product data, and the method comprises the following steps:
checking the basic information of the medicines corresponding to the initial medicine data through the basic information of the medicines corresponding to the medicine checking data, and if the initial medicine data accords with a preset checking standard, inputting the initial medicine data serving as standard data into a standard database;
wherein, the preset calibration standard comprises: and the basic information of the medicines corresponding to the initial medicine data is the same as the basic information of the medicines corresponding to the medicine verification data.
9. The method of claim 6, wherein the predetermined verification criteria comprises: under the condition that the initial medicine data is the same as the medicine verification data and the historical transaction data meets set conditions, the initial medicine data is used as standard product data to be recorded into a standard product database;
the method further comprises the following steps:
under the condition that the historical transaction data do not accord with the set conditions, inputting the initial standard data into an application and adding the initial standard data into a waiting state task set; the waiting state task set comprises at least one standard product data entry application, and historical transaction data corresponding to the standard product data entry application do not accord with the set conditions;
and polling and reading the standard product data entry application in the waiting state task set so as to take the initial drug data of the standard product data entry application as the standard product data entry standard product database under the condition that the historical transaction data corresponding to the standard product data entry application meets the set conditions.
10. The method of claim 9, wherein prior to entering the initial drug data of the initial label data entry application as label data into a label database, the method further comprises:
acquiring historical standard data entry application aiming at the medicine; the historical standard product data is input and applied with historical medicine data applied as standard product data;
merging the initial standard data entry application and the historical standard data entry application under the condition that the historical medicine data is the same as the initial medicine data.
11. A label data entry device for a pharmaceutical product, comprising:
the receiving module is used for receiving an initial standard data entry application of the medicine; wherein, the initial standard data entry application is accompanied with initial drug data applied as standard data; the standard data is used for characterizing the drug;
the acquisition module is used for acquiring historical transaction data of the medicine; wherein the historical transaction data comprises drug verification data of the drug; wherein the historical transaction data comprises transaction times for the drug;
the processing module is used for verifying the initial drug data through the drug verification data, and if the initial drug data accords with a preset verification standard, the initial drug data is used as standard data to be recorded into a standard database, and the method comprises the following steps: checking the initial medicine data through the medicine checking data and the transaction times of the medicines, and if the initial medicine data meet a preset checking standard, inputting the initial medicine data serving as standard product data into a standard product database; wherein, the preset calibration standard comprises: the initial medicine data are the same as the medicine verification data of the medicine, and the transaction times of the medicine are larger than a preset transaction time threshold value.
12. A label data entry device for a pharmaceutical product, comprising:
the receiving module is used for receiving an initial standard data entry application of the medicine; wherein, the initial standard data entry application is accompanied with initial drug data applied as standard data; the label data is used to characterize the drug;
the acquisition module is used for acquiring historical transaction data of the medicine; wherein the historical transaction data comprises drug verification data of the drug; wherein the historical transaction data comprises an associated pharmacy quantity of the drug;
the processing module is used for verifying the initial drug data through the drug verification data, and if the initial drug data accords with a preset verification standard, the initial drug data is used as standard data to be recorded into a standard database, and the method comprises the following steps: checking the initial medicine data through the medicine checking data and the number of the medicine stores related to the medicines, and if the initial medicine data meets a preset checking standard, inputting the initial medicine data serving as standard data into a standard database; wherein, the preset calibration standard comprises: the initial drug data is the same as drug verification data of the drugs, and the number of associated drug stores of the drugs is larger than a preset threshold value of the number of associated drug stores.
13. A computer device comprising a memory storing a computer program and a processor implementing the method of any one of claims 1 to 10 when executing the computer program.
14. A computer-readable storage medium, on which a computer program is stored which, when being executed by a processor, carries out the method of any one of claims 1 to 10.
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