期刊文献+

真实世界数据在上市后药品安全性监测和评价中的适用范围 被引量:2

Application Scope of Real-World Data in Post-Marketing Drug Safety Monitoring and Evaluation for Drug Safety
下载PDF
导出
摘要 目的分析真实世界数据(real-world data,RWD)在上市后药品安全性监测和评价中的应用现状,总结其适用范围。方法检索PubMed、Embase、中国生物医学文献服务系统、中国知网等数据库建库至2020年1月2日中与RWD及上市后药品安全性相关的文献并进行统计分析。结果RWD在上市后药品安全性监测和评价研究中适用范围主要体现在研究设计、药物类别、临床问题3个方面。结论RWD在上市后药品安全性监测和评价中适用范围广,充分合理利用RWD开展真实世界研究(real-world study,RWS),可为药品上市后安全性主动监测与评价开辟新途径。 Objective To analyze and summarize the application status of real-world data(RWD)in postmarketing drug safety monitoring and evaluation.Methods The literature related to RWD and post-marketing drug safety were searched and statistical analyzed in PubMed,Embase,SinoMed,CNKI and other databases from the establishment to January 2,2020.Results The scope of application of RWD in post-marketing drug safety monitoring and evaluation research is mainly reflected in 3 aspects,including research design,drug categories and clinical problems.Conclusion RWD has a wide range of applications in post-marketing drug safety monitoring and evaluation.The full and reasonable use of RWD to carry out real-world study(RWS)can open up a new way for the active monitoring and evaluation of drug safety after marketing.
作者 乔瑞 刘玉强 卓琳 孟若谷 孙凤 詹思延 QIAO Rui;LIU Yuqiang;ZHUO Lin;MENG Ruogu;SUN Feng;ZHAN Siyan(Research Center of Clinical Epidemiology,Peking University Third Hospital,Beijing 1001912,China;School of Public Health,Baotou Medical College of Inner Mongolia University of science and technology,Baotou 014040,China;Department of Pharmacy,Changzhi People's Hospital,Changzhi Shanxi 046000,China;National Institute of Health Data Science,Peking University,Beijing 100191,China;School of Public Health,Peking University,Beijing 100191,China)
出处 《中国药物警戒》 2021年第7期620-623,631,共5页 Chinese Journal of Pharmacovigilance
基金 国家自然科学基金资助项目(72074011、82003536) 国家药品监督管理局中国药品监管科学行动计划重点项目(CDRZ20193027)。
关键词 真实世界数据 适用范围 安全性评价 上市后药品监测 real-world data scope of application safety evaluation post-marketing drug monitoring
  • 相关文献

参考文献4

二级参考文献32

  • 1CFDA.药品不良反应报告和监测管理办法(卫生部令第81号)[EB/OL].(2011-05-04)[2014-06-23].http://www.sda.gov.cn/WS01/CL0053/62621.html. 被引量:4
  • 2张振,周毅,杜守洪,等.医疗大数据及其面临的机遇与挑战[J].医学信息学杂志,2014,35(6):1-8. 被引量:18
  • 3郭凡礼.开放大数据带动美国医疗革命[N].中国经营报,2014-06-16(A12). 被引量:1
  • 4Stang P E,Ryan P B5Racoosin J A,et al.Advancing the science for active surveillance:rationale and design for the Observational Medical Outcomes Partnershop[J].Annals oflntemalMedicine,2010,153(9):600-606. 被引量:1
  • 5FDA.FDA's Sentinel Initiative-Background[EB/OL].(2010-01-19)[2014-12-23].http://www.fda.gov/Safety/FD AsSentinelInitiative/ ucml49340.htm. 被引量:1
  • 6REAGAN-UD ALL FOUNDATIONJnnovationin Medical Evidence Development and Surveillance(IMEDS)Program[EB/OL].[2014-12-23].http://www.reaganudall.org/our-work/safety-and-better- evidence/imeds-program/. 被引量:1
  • 7HHS.Health Information Technology for Economic and Clinical Health Act[EB/OL].(2009-02-17)[2014-12-23].wwwJihs.gov/ocr/ privacy/hipaa/understanding/coveredentities/hitechact.pdf. 被引量:1
  • 8EMA.Pharmacovigilance legislation[EB/OL].(2010-12-31)[2014-12-23].http://www.ema.europa.eu/ema/index.jsp?curl=pages/special_top- ics/general/general_content_000491.jsp&mid=WC0b01ac058058f32d. 被引量:1
  • 9EMA.Objectives ofPROTECT[EB/OL].[2014-12-23].http://www.imi-protect.eu/objectives.shtml. 被引量:1
  • 10Yu-Lin Huang,Jinhee Moon,Jodi B Segal.A Comparison of Ac- tive Adverse Event Surveillance Systems Worldwide[J].DrugSaf,2014,37(8):581-596. 被引量:1

共引文献46

同被引文献18

引证文献2

二级引证文献14

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部