中国药物警戒 ›› 2015, Vol. 12 ›› Issue (10): 597-599.

• 药物警戒专栏 • 上一篇    下一篇

欧盟新版《药物警戒实践指南》中PSUR评估程序简介及启示

李科南1, 甄志芹1, 杜晓蕾2, 1, 冯亚楠2   

  1. 1.邢台市药品不良反应和药物滥用监测中心,河北 邢台054000;
    2.河北省药品监测评价中心,河北 石家庄 050000
  • 收稿日期:2015-07-21 修回日期:2015-12-07 出版日期:2015-10-08 发布日期:2015-12-07
  • 作者简介:李科南,男,硕士,医药工程师,药品不良反应监测。

Processes for PSUR Assessment in the European Union Network

LI Ke-nan1, ZHEN Zhi-qin1, DU Xiao-lei2, 1, FENG Ya-nan2   

  1. 1.Center for ADR Monitoring, Xingtai FDA, Hebei Xingtai 054000, China;
    2.Center for Drug Monitoring and Evaluation of Hebei, Hebei FDA, Hebei Shijiazhuang 050000, China
  • Received:2015-07-21 Revised:2015-12-07 Online:2015-10-08 Published:2015-12-07

摘要: 目的 对欧盟新版《药物警戒实践指南》中PSUR评估程序进行介绍,为促进和优化我国PSUR审核提供参考。方法 通过查阅欧盟药品管理局和国家食品药品监督管理总局网站信息及国内外PSUR评审程序相关文献资料,运用文献研究法进行分析。结果 欧盟药品管理局通过优化资源配置,对不同程序上市药品采用不同的PSUR评估方式,程序简化合理,协调和加强了欧洲经济区药品安全和利益风险审查。结论 我国应借鉴欧盟PSUR评估程序,提高我国药品安全监测能力。

关键词: 药物警戒实践指南, 药物警戒, 定期安全性更新报告, 评估

Abstract: Objective To provide reference for facilitating and optimizing China's periodic safety update report (PSUR) assessment according to the introduction of PSUR assessment process of European Union(EU) guideline on good pharmacovigilance practices(GVP). Methods Literature study was used to analyze the European Medicines Agency(EMA) and China Food and Drug Administration(CFDA) website information about PSUR assesment process. Results By optimizing the allocation of resources, the EU has adopted different PSUR assessment procedures for different medicinal products. This initiative aims to harmonize and strengthen the safety and benefit-risk review of medicines across the European Economic Area. Conclusion We should learn from EU processes for PSUR assessment to improve our ability to monitor drug safety.

Key words: guideline on good pharmacovigilance practices(GVP), pharmacovigilance, periodic safety update report, assessment

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