Auxiliary reporting method of adverse drug reaction data and related equipment

Abstract

The invention discloses an auxiliary reporting method for adverse drug reaction data and related equipment, which can be applied to the technical field of drug data processing. According to the application, the adverse drug reaction auxiliary reporting system is deployed on each first terminal, and after the adverse drug reaction auxiliary reporting system is set to be connected with the intermediate library through the preset transmission data standard, the authentication certificate corresponding to the first terminal is generated in response to the connection request instruction of the first terminal; therefore, the influence of network fluctuation on the adverse drug reaction auxiliary reporting system can be reduced, then various instructions of the adverse drug reaction data report are responded, and the corresponding interface is displayed, so that a user can fill in data of the adverse drug reaction data report in the corresponding interface, the user does not need to edit the report format, and the user experience is improved. The efficiency and real-time performance of drug adverse reaction data transmission are effectively improved, and the workload of a user is reduced.

Description

TECHNICAL FIELD

[0001] The present application relates to the technical field of drug data processing, and in particular to a method for assisting in reporting of drug adverse reaction data and related equipment. BACKGROUND

[0002] In related technologies, in the reporting process of drug adverse reaction data by medical institutions, a web version system is mainly used to manually fill in the web version drug adverse reaction (ADR) report in the national drug adverse reaction monitoring system on the Internet. Since the web filling process has a high requirement for the stability of the network, the ADR filling process and feedback are easily affected by the network, thereby affecting the information transmission efficiency and real-time performance. Meanwhile, a large amount of content needs to be filled in for an ADR report, and if a user needs to process multiple ADR reports, the user needs to spend a large amount of time, thereby increasing the workload of the user and reducing the overall work efficiency. In addition, the format of the reported ADR report is difficult to unify, thereby possibly leading to repeated modification operations, further increasing the workload of the user.

[0003] To sum up, the technical problems in related technologies need to be improved. SUMMARY

[0004] The main purpose of the embodiments of the present application is to provide a method for assisting in reporting of drug adverse reaction data and related equipment, which can effectively improve the efficiency and real-time performance of the transmission of drug adverse reaction data and reduce the workload of the user.

[0005] To achieve the above purpose, one aspect of the embodiments of the present application provides a method for assisting in reporting of drug adverse reaction data, which comprises the following steps:

[0006] In response to a connection request instruction of a plurality of first terminals, an authentication certificate corresponding to the first terminal is generated, each of the first terminals is deployed with a drug adverse reaction assisting reporting system, and the drug adverse reaction assisting reporting system is connected with an intermediate library through a preset data transmission standard;

[0007] In response to a first processing instruction of a drug adverse reaction data report, a first processing interface of the drug adverse reaction data report is displayed, and the first processing interface is used to guide the user to process the data of the drug adverse reaction data report;

[0008] In response to a new report request instruction of the reporting interface, a report filling interface in a preset format is displayed, the report filling interface is used to guide the user to perform a data filling process of the drug adverse reaction data report, and the filled drug adverse reaction data is sent to the intermediate library.

[0009] In some embodiments, the method further comprises the following steps:

[0010] In response to the new report request instruction of the reporting interface, a basic information filling sub-interface in the report filling interface is displayed, and the basic information filling sub-interface is used to guide the user to fill in the basic information in the drug adverse reaction data report.

[0011] In response to the new report request instruction of the reporting interface, a patient information filling sub-interface in the report filling interface is displayed, and the patient information filling sub-interface is used to guide the user to fill in the patient information in the drug adverse reaction data report.

[0012] In some embodiments, the method further comprises the following steps:

[0013] In response to the temporary report operation instruction of the reporting interface, a temporary report interface in a preset format is displayed, and the temporary report interface is used to guide the user to view, improve or modify the temporary report.

[0014] In some embodiments, the method further comprises the following steps:

[0015] In response to the report list viewing instruction of the reporting interface, a report list interface is displayed, and the report list interface is used to display summary entries corresponding to all drug adverse reaction data reports, and the summary entries are associated with the corresponding drug adverse reaction data reports through a preset link.

[0016] In some embodiments, the method further comprises the following steps:

[0017] In response to the management instruction of the drug adverse reaction data report, a management selection interface of the drug adverse reaction data report is displayed, and the management selection interface is used to guide the user to perform management operations on the drug adverse reaction data report, and the management operations include pending report management operations and processed report management operations.

[0018] In some embodiments, in response to the management instruction of the drug adverse reaction data report, the management selection interface of the drug adverse reaction data report is displayed, which comprises:

[0019] In response to the pending report operation instruction in the management instruction of the drug adverse reaction data report, a pending report management selection interface of the drug adverse reaction data report is displayed.

[0020] In response to the condition query instruction of the pending report management selection interface, all pending report interfaces corresponding to the condition query instruction are displayed.

[0021] In some embodiments, the method further comprises the following steps:

[0022] In response to a second processing instruction of the adverse drug reaction data report, a second processing interface of the adverse drug reaction data report is displayed, and the second processing interface is used to guide a user to perform reported list viewing, report table searching, report perfecting, or report deletion searching.

[0023] In some embodiments, the method further comprises the following steps:

[0024] In response to a query instruction of the adverse drug reaction data report, a query interface of the adverse drug reaction data report is displayed, and the query interface is used to guide a user to perform query condition filling and query report downloading.

[0025] To achieve the above object, another aspect of the embodiment of the present application provides an adverse drug reaction data auxiliary reporting device, which comprises:

[0026] A generation module is configured to generate an authentication certificate corresponding to a plurality of first terminals in response to a connection request instruction of the first terminals, each of the first terminals being deployed with an adverse drug reaction auxiliary reporting system, and the adverse drug reaction auxiliary reporting system being connected to an intermediate library through a preset data transmission standard.

[0027] A first display module is configured to display a first processing interface of the adverse drug reaction data report in response to a first processing instruction of the adverse drug reaction data report, and the first processing interface is used to guide a user to perform data processing of the adverse drug reaction data report.

[0028] A second display module is configured to display a report filling interface in a preset format in response to a new report request instruction of the reporting interface, and the report filling interface is used to guide a user to perform a data filling process of the adverse drug reaction data report and send the filled adverse drug reaction data to the intermediate library.

[0029] To achieve the above object, another aspect of the embodiment of the present application provides an electronic device, which comprises a memory and a processor, the memory stores a computer program, and the processor implements the above method when executing the computer program.

[0030] To achieve the above object, another aspect of the embodiment of the present application provides a computer readable storage medium, which stores a computer program, and the computer program is executed by a processor to implement the above method.

[0031] To achieve the above object, another aspect of the embodiment of the present application provides a computer program product, which comprises a computer program, and the computer program is executed by a processor to implement the above method

[0032] The embodiments of the present application at least have the following beneficial effects: the present application provides a method and related device for assisting in reporting adverse drug reaction data, the scheme is that an adverse drug reaction assisting reporting system is deployed on each first terminal, and the adverse drug reaction assisting reporting system is connected with an intermediate library through a preset data transmission standard, and an authentication certificate corresponding to the first terminal is generated in response to a connection request instruction of the first terminal, so that the influence of network fluctuation on the adverse drug reaction assisting reporting system is reduced, then a first processing interface of the adverse drug reaction data report is displayed in response to a first processing instruction of the adverse drug reaction data report, so that the user can process the data of the adverse drug reaction data report in the interface, then a report filling interface in a preset format is displayed in response to a new report request instruction of the reporting interface, so that the user can fill in the data of the adverse drug reaction data report in the interface, thereby the user does not need to edit the report format by himself, the efficiency and real-time performance of the adverse drug reaction data transmission are effectively improved, and the workload of the user is reduced. BRIEF DESCRIPTION OF DRAWINGS

[0033] Figure 1 is a flowchart of the method for assisting in reporting adverse drug reaction data provided by the embodiments of the present application;

[0034] Figure 2 is a schematic diagram of a report filling interface provided by the embodiments of the present application;

[0035] Figure 3 is a schematic diagram of a to-be-processed report management selection interface provided by the embodiments of the present application;

[0036] Figure 4 is an interface schematic diagram of a reported list provided by the embodiments of the present application;

[0037] Figure 5 is a query interface schematic diagram of an adverse drug reaction data report provided by the embodiments of the present application;

[0038] Figure 6 is a structural schematic diagram of an adverse drug reaction data assisting reporting device provided by the embodiments of the present application. DETAILED DESCRIPTION

[0039] In order to make the purposes, technical solutions and advantages of the present application clearer, the present application will be further described in detail below with reference to the drawings and embodiments. It should be understood that the specific embodiments described herein are only used to explain the present application and not intended to limit the present application. When the following description refers to the drawings, the same numbers in different drawings represent the same or similar elements unless otherwise indicated. The implementations described in the following exemplary embodiments do not represent all implementations consistent with embodiments of the present application. They are only examples of devices and methods consistent with some aspects of embodiments of the present application.

[0040] It can be understood that the terms "first", "second", and the like used in the present application can be used herein to describe various concepts, but unless specifically stated, these concepts are not limited by these terms. These terms are only used to distinguish one concept from another. For example, without departing from the scope of embodiments of the present application, the first information can also be referred to as the second information, and similarly, the second information can also be referred to as the first information. Depending on the context, the word "if" as used herein can be interpreted as "when" or "when" or "in response to determining".

[0041] The terms "at least one", "multiple", "each", "any" and the like used in the present application include one, two or more than two, multiple includes two or more than two, each refers to each of the corresponding multiple, and any refers to any one of the multiple.

[0042] Unless otherwise defined, all technical and scientific terms used herein have the same meaning as understood by those skilled in the art to which the present application belongs. The terms used herein are only for the purpose of describing the embodiments of the present application and are not intended to limit the present application.

[0043] Before the embodiments of the present application are described in detail, first, some nouns and terms involved in the embodiments of the present application are described, and the nouns and terms involved in the embodiments of the present application are applicable to the following explanations:

[0044] Adverse Drug Reactions (ADR) refers to the occurrence of adverse reactions, including side effects, toxicity reactions, allergic reactions, after effects, etc. unrelated to the purpose of drug use or unexpected harmful reactions of qualified drugs under normal usage and dosage.

[0045] E2B data standard is an electronic transmission specification developed by international drug regulatory agencies (such as WHO) for standardizing the electronic report format in adverse drug reaction monitoring.

[0046] E2B(R3) is a core standard for electronic transmission of individual case safety reports (ICSR) established by the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH), aiming to regulate the global exchange of drug safety data.

[0047] The concept of electronic data interchange (EDI) in medical institutions mainly involves efficient and secure transmission of medical data through standardized formats to improve the efficiency and quality of medical services. EDI is a technology that transmits standardized medical documents (such as electronic medical records, prescriptions, test reports, etc.) through computer networks, using international standard formats such as ANSI, to ensure accurate analysis and processing of data between different medical institutions.

[0048] In related technologies, during the reporting process of adverse drug reaction data by medical institutions, the filling of web-based adverse drug reaction (ADR) reports in the national adverse drug reaction monitoring system on the Internet is mainly completed manually through a web-based system. Since the web-based filling process has high requirements for network stability, the ADR filling process and feedback are easily affected by the network, thereby affecting the efficiency and real-time performance of information transmission. At the same time, a large amount of content needs to be filled in an ADR report, and if a user needs to process multiple ADR reports, the user will spend a lot of time, thereby increasing the user's workload and reducing overall work efficiency. In addition, the format of the reported ADR report is difficult to unify, which may lead to repeated modification operations, further increasing the user's workload.

[0049] Therefore, the embodiments of the present application provide an auxiliary reporting method for adverse drug reaction data and related equipment, which can effectively improve the efficiency and real-time performance of adverse drug reaction data transmission and reduce the user's workload.

[0050] The auxiliary reporting method for adverse drug reaction data provided by the embodiments of the present application relates to the technical field of drug data processing. The auxiliary reporting method for adverse drug reaction data provided by the embodiments of the present application can be applied in a terminal, can be applied in a server, and can also be software running in a terminal or a server. In some embodiments, the terminal can be a smart phone, a tablet computer, a notebook computer, a desktop computer, a smart speaker, a smart watch, a vehicle-mounted terminal, etc., but is not limited thereto; the server end can be configured as a standalone physical server, can be configured as a server cluster or a distributed system composed of multiple physical servers, can be configured as a cloud server providing cloud services, cloud databases, cloud computing, cloud functions, cloud storage, network services, cloud communication, middleware services, domain name services, security services, CDNs, and basic cloud computing services such as big data and artificial intelligence platforms, and the server can also be a node server in a blockchain network; the software can be an application that implements the auxiliary reporting method for adverse drug reaction data, etc., but is not limited to the above forms.

[0051] The application is operable in a variety of general purpose or special purpose computing system environments or configurations. Examples of well-known computing systems, environments, and / or configurations that can be suitable for use with the application include personal computers, server computers, handheld or laptop devices, tablet devices, multiprocessor systems, microprocessor-based systems, set top boxes, programmable consumer electronics, network PCs, minicomputers, mainframe computers, distributed computing environments that include any of the above systems or devices, and the like. The application can be described in the general context of computer-executable instructions, such as program modules, being executed by a computer. Generally, program modules include routines, programs, objects, components, data structures, and the like, that perform particular tasks or implement particular abstract data types. The application can also be practiced in distributed computing environments where tasks are performed by remote processing devices that are linked through a communications network. In a distributed computing environment, program modules can be located in local and remote computer storage media including memory storage devices.

[0052] It should be noted that in each specific embodiment of the present application, when relevant processing needs to be performed on data related to the identity or characteristics of the user, such as user information, user behavior data, user history data, and user location information, the user's permission or consent will be obtained first, and the collection, use, and processing of such data will comply with relevant laws, regulations, and standards. In addition, when the embodiments of the present application need to obtain sensitive personal information of the user, the separate permission or separate consent of the user will be obtained through a pop-up window or a jump to a confirmation page, and after obtaining the separate permission or separate consent of the user, the necessary user-related data for enabling the embodiments of the present application to function normally will be obtained.

[0053] The embodiments of the present application will be described in detail below with reference to the accompanying drawings:

[0054] Figure 1 is an optional flowchart of the method for assisting in reporting adverse drug reaction data provided by the embodiments of the present application, Figure 1 The method in can include but is not limited to including steps S110 to S130:

[0055] Step S110, in response to a connection request instruction of a plurality of first terminals, generating an authentication certificate corresponding to the first terminal, wherein each first terminal is deployed with an adverse drug reaction assisting reporting system, and the adverse drug reaction assisting reporting system is connected with an intermediate library through a preset data transmission standard;

[0056] Step S120, in response to a first processing instruction of the adverse drug reaction data report, displaying a first processing interface of the adverse drug reaction data report, wherein the first processing interface is used to guide the user to process the data of the adverse drug reaction data report;

[0057] Step S130: In response to the new report request instruction on the reporting interface, a report filling interface in a preset format is displayed. The report filling interface is used to guide the user in the data filling process of the adverse drug reaction data report and to send the filled adverse drug reaction data to the intermediate database.

[0058] It is understandable that the intermediate database refers to a database with a standard table structure. Hospitals that have deployed this implementation method import and push business data into this intermediate database with a unified table structure, based on the actual database table format of their respective hospital information systems, and then perform subsequent data processing according to the method of this embodiment.

[0059] The preset data transmission standard can be the data transmission standard of the medical institution's EDI electronic data gateway. In this embodiment, the first terminal can be a hospital service device. When the adverse drug reaction auxiliary reporting system is installed in the hospital service device according to the technical documentation and installation package, gateway team members can generate corresponding authentication certificates through the gateway management platform, enabling the adverse drug reaction auxiliary reporting system in the hospital service device to perform autonomous reporting of adverse drug reaction reports.

[0060] It is understood that after the installation and connection of the adverse drug reaction reporting system are completed in this embodiment, the corresponding users can independently fill in adverse drug reaction data reports on the system. Specifically, in the process of responding to the new report request instruction on the reporting interface and displaying the report filling interface in a preset format, this embodiment includes, but is not limited to, the following steps:

[0061] In response to the new report request command on the reporting interface, the basic information filling sub-interface in the report filling interface is displayed. The basic information filling sub-interface is used to guide users to fill in the basic information in the adverse drug reaction data report.

[0062] In response to the new report request command on the reporting interface, the patient information entry sub-interface in the report entry interface is displayed. The patient information entry sub-interface is used to guide users in entering patient information in the adverse drug reaction data report.

[0063] For example, such as Figure 2 As shown, after entering the "Adverse Reaction Report" interface, users can click the "Individual Case Report" control to trigger a request for an individual adverse drug reaction data report to the backend. When the user clicks the "New Report" control in the "Individual Case Report" subpage, a new report request command is sent to the backend, allowing the backend to retrieve the corresponding interface content based on this command, thereby controlling the display of the currently retrieved content. Figure 2As shown, after sending the new report request instruction to the backend, the front-end interface displays the report filling interface of "new report". The report filling interface includes, but is not limited to, a basic information filling sub-interface and a patient information filling sub-interface. In the basic information filling sub-interface, the user can select the report type and the report unit category according to the prompt information of the interface, and fill in the hospital name. In the patient information filling sub-interface, the user can select the patient type and the patient gender, and fill in one or more of the patient weight, medical record number, patient name, nationality, birth date, contact information, etc.

[0064] It can be understood that when the operation of the individual report is performed, the embodiment will also display a temporary report interface in a preset format in response to the temporary report operation instruction of the reporting interface, so as to guide the user to view, improve or modify the temporary report through the temporary report interface. For example, when the user fills in the adverse drug reaction data report, if it is found that the data is incomplete at this time, a temporary report can be generated based on the filled data, so that the corresponding report in the temporary report can be continuously improved when the subsequent data is obtained. For example, when the user fills in the report, it is found that some data is questionable, a temporary report can be generated based on the current data, and then the temporary report is modified after the correct data is obtained. Through the setting of the temporary report, the user can fill in the data in time and improve it later, so as to improve the accuracy of the final report.

[0065] It can be understood that after obtaining one or more reports, the embodiment can display a report list interface in response to the report list viewing instruction of the reporting interface, and then display the summary entries corresponding to all adverse drug reaction data reports through the report list interface. The summary entry is associated with the corresponding adverse drug reaction data report through a preset link. Specifically, the summary entry of the embodiment can display the basic detail information of the report. When the basic detail information is clicked, the corresponding adverse drug reaction data report can be called and displayed through a preset link relationship. The preset link relationship of the embodiment can be realized by a hyperlink.

[0066] It is understood that this embodiment can also respond to the management instructions of adverse drug reaction data reports by displaying a management selection interface for adverse drug reaction data reports, thereby guiding the user to perform management operations on the adverse drug reaction data reports through the management selection interface. These management operations include pending report management operations and processed report management operations. Specifically, when displaying the management selection interface, this embodiment can display the pending report management selection interface for adverse drug reaction data reports in response to the pending report operation instructions in the management instructions for adverse drug reaction data reports. Then, in response to the conditional query instructions in the pending report management selection interface, it can display all pending report interfaces corresponding to the conditional query instructions. For example, as shown... Figure 3 As shown, when a user clicks the "Pending Reports" control in the management selection interface, the backend receives a pending report operation instruction and controls the frontend to display the pending report management selection interface based on this instruction. When the user enters corresponding query information in the "Conditional Query" box of the pending report management selection interface, such as entering the report submission time as April 1, 2023 - April 1, 2024, the backend receives a conditional query instruction triggered by the frontend based on the input information, and uses this instruction to count the information of all pending reports. Then, based on the information of the pending reports, it controls the display content of the pending report interface. Figure 3 As can be seen, the pending reports interface displays the number of unreviewed reports, the number of reviewed reports, the number of reports being sent, and the number of reports that failed to be sent. When the user clicks the corresponding report type query control, such as clicking the "Unreviewed" control, the display box of the pending reports interface will show summary information of all unreviewed reports corresponding to the conditional query command, thus making it convenient for the user to view the content of unreviewed reports in a timely manner and improving the user's work efficiency.

[0067] It can be understood that the embodiment can also display a second processing interface of the adverse drug reaction data report in response to a second processing instruction of the adverse drug reaction data report, so as to guide the user to perform reported list viewing, report table searching, report perfecting, or deleting report searching through the second processing interface. Specifically, the first processing instruction can be an instruction triggered by the user at the hospital end in the system, and the first processing interface can be a user operation interface at the hospital end. The second processing instruction can be an instruction triggered by a terminal user corresponding to the adverse drug reaction detection (ADR) center in the system, and the second processing interface can be a user operation interface at the device end corresponding to the adverse drug reaction detection (ADR) center. The second processing interface of the embodiment can view the existing report, search the report, perfect the report, or delete the useless report. In the embodiment, after the user at the hospital end completes the filling and uploading of the report, the uploaded data is saved in the intermediate library. When the adverse drug reaction detection (ADR) center end needs to analyze the adverse drug reaction, the data in the intermediate library can be called by the system to perform analysis. Since the ends are not directly connected, the security of the privacy data in the ends can be ensured.

[0068] In the use process of the second processing interface, for example, when the user clicks the "reported list" control of the second processing interface, as shown in Figure 4 , the second processing interface displays the details of the reported list. As can be seen from Figure 4 , the user can input the query condition in the "condition query" box, and the back end can call the corresponding reported information according to the query condition and generate a reported list for display. Each report in the reported list corresponds to the report table code, patient information, report type, generic name, adverse reaction name, and other information, so as to facilitate the user to quickly understand the information of each report.

[0069] It can be understood that the embodiment will also display a query interface of the adverse drug reaction data report in response to a query instruction of the adverse drug reaction data report, so as to guide the user to fill in the query condition and download the query report through the query interface. For example, when the user clicks the "comprehensive query" control, the back end receives the query instruction sent by the front end, and performs a comprehensive query process of the report based on the query instruction. For example, as shown in Figure 5 , the user can input the corresponding query condition in the "condition query" box of the query interface, and the back end can call all original reports meeting the query condition based on the query condition and display a list of the original reports. When the user views the report to be downloaded in the displayed list, the user can automatically download the original report by checking the corresponding report entry in the list and clicking the "original report download" control, so as to effectively improve the work efficiency of the user.

[0070] It can be known from the above that the method of the embodiment of the application sets the display interface in the preset format, so that the user can complete the report filling, query and other operations in the interface, thereby ensuring the uniformity of the report format, improving the efficiency and real-time performance of the drug adverse reaction data transmission, and reducing the workload of the user.

[0071] Please refer to Figure 6 The embodiment of the application also provides an auxiliary reporting device for drug adverse reaction data, which comprises:

[0072] The generating module 610 is configured to generate an authentication certificate corresponding to each first terminal in response to a connection request instruction of the first terminal, each first terminal being deployed with a drug adverse reaction auxiliary reporting system, and the drug adverse reaction auxiliary reporting system being connected to the intermediate library through a preset data transmission standard.

[0073] The first display module 620 is configured to display a first processing interface of the drug adverse reaction data report in response to a first processing instruction of the drug adverse reaction data report, the first processing interface being used to guide the user to process the data of the drug adverse reaction data report.

[0074] The second display module 630 is configured to display a report filling interface in a preset format in response to a new report request instruction of the reporting interface, the report filling interface being used to guide the user to fill in the data of the drug adverse reaction data report and send the filled drug adverse reaction data to the intermediate library.

[0075] It can be understood that the content in the above method embodiment is applicable to the device embodiment, the device embodiment specifically implements the same functions as the above method embodiment, and achieves the same beneficial effects as the above method embodiment.

[0076] The embodiment of the application also provides an electronic device, which comprises a memory and a processor, the memory stores a computer program, and the processor implements the above method when executing the computer program. The electronic device can be any intelligent terminal, such as a tablet computer or a vehicle-mounted computer.

[0077] It can be understood that the content in the above method embodiment is applicable to the device embodiment, the device embodiment specifically implements the same functions as the above method embodiment, and achieves the same beneficial effects as the above method embodiment.

[0078] The embodiment of the application also provides a computer readable storage medium, which stores a computer program, and the computer program is executed by a processor to implement the above method.

[0079] It can be understood that the contents in the above method embodiments are all applicable to the present storage medium embodiments, the present storage medium embodiments specifically implement the functions same as those of the above method embodiments, and achieve the beneficial effects same as those of the above method embodiments.

[0080] The present application also provides a computer program product, comprising a computer program, which, when executed by a processor, implements the above method.

[0081] It can be understood that the contents in the above method embodiments are all applicable to the present program product embodiments, the present program product embodiments specifically implement the functions same as those of the above method embodiments, and achieve the beneficial effects same as those of the above method embodiments.

[0082] The memory, as a non-transitory computer readable storage medium, can be used to store non-transitory software programs and non-transitory computer executable programs. In addition, the memory can include a high-speed random access memory, and can also include a non-transitory memory, such as at least one magnetic disk storage device, a flash memory device, or other non-transitory solid-state memory device. In some embodiments, the memory can optionally include a memory disposed remotely relative to the processor, and these remote memories can be connected to the processor through a network. Examples of the above network include but are not limited to the Internet, an intranet, a local area network, a mobile communication network, and combinations thereof.

[0083] The embodiments described in the present application are for more clearly illustrating the technical solutions of the present application, and do not constitute a limitation on the technical solutions provided by the present application. Those skilled in the art can know that, with the evolution of technology and the appearance of new application scenarios, the technical solutions provided by the present application are also applicable to similar technical problems.

[0084] Those skilled in the art can understand that the technical solutions shown in the figures do not constitute a limitation on the present application, and can include more or fewer steps than shown in the figures, or combine certain steps, or different steps.

[0085] The device embodiments described above are only schematic, and the units described as separate components can or can not be physically separate, i.e., can be located in one place, or can be distributed on multiple network units. Part or all of the modules can be selected according to actual needs to achieve the purposes of the present embodiments.

[0086] Those skilled in the art can understand that all or some of the steps in the above disclosed method, the functional modules / units in the system and the device can be implemented as software, firmware, hardware and their appropriate combinations.

[0087] The terms "first", "second", "third", "fourth", and the like in the description and in the claims of this application, if any, are used for distinguishing between similar elements and not necessarily for describing a particular sequential or chronological order. It is to be understood that the use of the terms so termed is interchangeable under appropriate circumstances such that the embodiments of the application described herein are, for example, capable of orderly or chronological mundane operation, reverse order operation, based on circuitry availability, based on stated preference or the like, and that "default" or other orderings are thus permissible. Further, the terms "comprise", "comprising", "include", "including", and the like, are specifically intended to be open-ended. That is, references to individual steps and the like do not suhstantially exclude the presence of two or more of a given step or its integral presence in the process, method, system, article, or apparatus having been made with a wider scope. The use of notation such as "first", "second", "third", etc. does not generally limit the areas, but can be used for clarity, and merely establishes the order unless otherwise stated below.

[0088] It should be understood that, in the application, "at least one" means one or more, and "multiple" means two or more. "And / or" is used to describe the relationship between associated objects, which means that there can be three relationships, for example, "A and / or B" can mean that there are only A, only B, and A and B at the same time, where A and B can be singular or plural. The character " / " generally represents an "or" relationship between the associated objects. "At least one of the following" or the like means any combination of these items, including any combination of single or multiple items. For example, at least one of a, b or c can mean a, b, c, "a and b", "a and c", "b and c", or "a and b and c", where a, b, and c can be single or multiple.

[0089] In several embodiments provided in the application, it should be understood that the disclosed devices and methods can be implemented in other ways. For example, the device embodiments described above are only schematic, for example, the division of the above units is only a logical function division, and actual implementation can have another division manner, for example, a plurality of units or components can be combined or integrated into another system, or some features can be omitted or not executed. In addition, the coupling or direct coupling or communication connection between the displayed or discussed objects can be indirect coupling or communication connection through some interfaces, devices or units, which can be electrical, mechanical or other forms.

[0090] The units described above as separate components can or can not be physically separate, and the components shown as units can or can not be physical units, i.e. they can be located in one place or distributed on a plurality of network units. Part or all of the units can be selected according to actual needs to achieve the purpose of the embodiment.

[0091] In addition, each of the functional units in the embodiments of the present application can be integrated in one processing unit, or each unit can exist alone physically, or two or more units can be integrated in one unit. The integrated unit can be implemented in the form of hardware, or in the form of a software functional unit.

[0092] If the integrated unit is implemented in the form of a software functional unit and sold or used as an independent product, it can be stored in a computer readable storage medium. Based on such an understanding, the technical solutions of the present application, essentially or partially, or all or part of the technical solutions can be embodied in the form of a software product. The computer software product is stored in a storage medium, and includes multiple instructions used to cause a computer device (such as a personal computer, a server, or a network device) to perform all or part of the steps of the methods in the embodiments of the present application. The foregoing storage medium includes: various memories (such as a read-only memory, a random access memory, a flash memory, or the like) and a magnetic disk or an optical disk and the like.

[0093] The preferred embodiments of the embodiments of the present application are described above with reference to the accompanying drawings, and are not intended to limit the scope of the embodiments of the present application. Any modification, equivalent replacement, and improvement made by those skilled in the art without departing from the scope and spirit of the embodiments of the present application shall fall within the scope of the embodiments of the present application.

Claims

1. An auxiliary reporting method of adverse drug reaction data, characterized in that, The method comprises the following steps: In response to the connection request instructions of a plurality of first terminals, generate authentication certificates corresponding to the first terminals, each of which is deployed with an adverse drug reaction auxiliary reporting system, and the adverse drug reaction auxiliary reporting system is connected with the intermediate library through a preset data transmission standard; In response to the first processing instructions of the adverse drug reaction data reports, display the first processing interface of the adverse drug reaction data reports, which is used to guide the user to process the adverse drug reaction data reports; In response to the new report request instructions of the reporting interface, display the report filling interface in a preset format, which is used to guide the user to fill in the adverse drug reaction data reports, and send the filled adverse drug reaction data to the intermediate library.

2. The method of claim 1, wherein, The method further comprises the following steps: In response to the new report request instructions of the reporting interface, display the basic information filling sub-interface in the report filling interface, which is used to guide the user to fill in the basic information in the adverse drug reaction data reports; In response to the new report request instructions of the reporting interface, display the patient information filling sub-interface in the report filling interface, which is used to guide the user to fill in the patient information in the adverse drug reaction data reports.

3. The method of claim 1, wherein, The method further comprises the following steps: In response to the temporary report operation instructions of the reporting interface, display the temporary report interface in a preset format, which is used to guide the user to view, improve or modify the temporary report.

4. The method of claim 1, wherein, The method further comprises the following steps: In response to the report list viewing instructions of the reporting interface, display the report list interface, which is used to display the summary entries corresponding to all adverse drug reaction data reports, and the summary entries are associated with the corresponding adverse drug reaction data reports through a preset link.

5. The method of claim 1, wherein, The method further comprises the following steps: In response to the management instructions of the adverse drug reaction data reports, display the management selection interface of the adverse drug reaction data reports, which is used to guide the user to manage the adverse drug reaction data reports, and the management operations include the pending report management operation and the processed report management operation.

6. The method of claim 5, wherein, The method further comprises the following steps: In response to the management instructions of the adverse drug reaction data reports, display the management selection interface of the adverse drug reaction data reports, which is used to guide the user to manage the adverse drug reaction data reports, and the management operations include the pending report management operation and the processed report management operation. The method further comprises the following steps:

7. The method of claim 1, wherein, In response to the management instructions of the adverse drug reaction data reports, display the management selection interface of the adverse drug reaction data reports, which is used to guide the user to manage the adverse drug reaction data reports, and the management operations include the pending report management operation and the processed report management operation. In response to a second processing instruction of the drug adverse reaction data report, a second processing interface of the drug adverse reaction data report is displayed, and the second processing interface is used to guide a user to perform reported list viewing, report table searching, report perfecting or report searching.

8. The method of claim 1, wherein, The method further comprises the following steps: In response to a query instruction of the drug adverse reaction data report, a query interface of the drug adverse reaction data report is displayed, and the query interface is used to guide a user to perform query condition filling and query report downloading.

9. An electronic device, comprising: The electronic device comprises a memory and a processor, the memory stores a computer program, and the processor implements the method in any one of claims 1 to 8 when executing the computer program.

10. A computer-readable storage medium storing a computer program, the computer program comprising instructions that, when executed by a computer, cause the computer to perform the method of any one of claims 1 to 9. The computer program is executed by the processor to implement the method in any one of claims 1 to 7.

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