基于FAERS数据库的艾塞那肽微球不良事件信号挖掘与研究
投稿时间:2024-03-28  修订日期:2024-07-10  点此下载全文
引用本文:张莲卿,骆岩,杨提,姚佳晨,李文艳.基于FAERS数据库的艾塞那肽微球不良事件信号挖掘与研究[J].药学实践杂志,2024,42(10):445~450
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作者单位E-mail
张莲卿 海军军医大学第一附属医院药剂科, 上海 200433  
骆岩 上海市浦东新区公利医院临床药学部, 上海 200135  
杨提 上海市浦东新区公利医院临床药学部, 上海 200135  
姚佳晨 上海市浦东新区公利医院临床药学部, 上海 200135  
李文艳 上海市浦东新区公利医院临床药学部, 上海 200135 liwenyan_linda@163.com 
基金项目:上海市浦东新区卫健委重点学科(PWZxk2022-26);上海市卫健委卫生行业临床研究专项青年项目(20214Y0400)
中文摘要:目的 运用美国FDA不良事件报告系统(FAERS)挖掘艾塞那肽微球使用中不良事件(ADE)风险信号,为临床合理用药和保障用药安全提供参考。方法 以“艾塞那肽微球”为目标药物,检索关键词为“exenatide microspheres for injection”“LY05006”“AC 2993 LAR”及“bydureon”,利用SAS软件提取FAERS数据库中2012年1月2日至2023年3月31日的ADE报告数据并去重,采用报告比值比法与综合标准法对艾塞那肽微球相关ADE报告进行数据挖掘。结果 共检索到艾塞那肽微球ADE报告27 248份,涉及 27个 系统器官分类,其中严重ADE报告4 719份。上报人员以消费者为主(18 435例,占67.66%),上报国家以美国为主(26 295例,占96.50%)。采用报告比值比法(ROR)与综合标准法(MHRA)共获得163个ADE风险信号,包括血胆固醇异常、脂肪酶升高及混合型高脂血症等新发不良反应。结论 基于FAERS数据库对艾塞那肽微球上市后的ADE进行挖掘分析,可对临床用药安全和提高患者用药依从性提供参考。
中文关键词:艾塞那肽微球  FDA不良事件报告系统  数据挖掘
 
Mining and research on the adverse event signal of exenatide microspheres based on FAERS database
Abstract:Objective To explore the risk signals of adverse events (ADE) in the use of exenatide microspheres by the FDA adverse event reporting system (FAERS), and provide reference for clinical rational drug use and drug safety. Methods With exenatide microspheres as the target drug, the search keywords were Exenatide Microspheres for Injection, LY05006 , AC 2993 LAR and Bydureon. SAS software was used to extract the ADE report data from January 2, 2012 to March 31, 2023 in the FAERS database and the duplicates were removed. Data mining of exenatide microspheres-related ADE reports was performed by the reporting odds ratio method and the comprehensive standard method. Results A total of 27 248 exenatide microspheres-related ADE reports were retrieved, involving 27 SOCs, of which 4 719 were severe ADE reports. The reporting personnel were mainly consumers (18 435 cases,67.66%), the United States was the mainly reporting country (26 295 cases,96.50%). A total of 163 ADE risk signals were obtained by reporting odds ratio method and comprehensive standard method, including new adverse reactions such as abnormal blood cholesterol, elevated lipase and mixed hyperlipidemia. Conclusion Based on the FAERS database, the post-marketing ADE of exenatide microspheres was mined and analyzed, which could provide reference for clinical medication safety and improvement of patients' medication compliance.
keywords:exenatide microspheres  FDA adverse event reporting system  data mining
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