中国药物警戒 ›› 2012, Vol. 9 ›› Issue (4): 224-226.

• 管理及工作研究 • 上一篇    下一篇

医疗机构如何做好药品不良反应监测工作

刘翠丽，田春华，冯红云   

  1. 国家食品药品监督管理局药品评价中心，北京 100045
  • 出版日期:2012-04-10 发布日期:2015-08-10
  • 作者简介:刘翠丽，女，硕士研究生，药品不良反应监测。

How Medical Institutions to Do Adverse Drug Reaction Monitoring Well

LIU Cui-li, TIAN Chun-hua, FENG Hong-yun   

  1. Center for Drug Reevaluation, SFDA, Beijing 100045, China
  • Online:2012-04-10 Published:2015-08-10

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摘要： 2011年5月4日，新修订的《药品不良反应报告和监测管理办法》正式颁布。新《办法》对药品不良反应的报告主体之一的医疗机构的职责进行了明确规定。本文旨在结合新《办法》，探讨医疗机构在现今新的药品不良反应监测形式下如何做好监测工作。

关键词: 医疗机构, 药品不良反应监测报告和监测管理办法, 药品不良反应监测

Abstract: The new revision of Provisions for Adverse Drug Reaciton Reporting and Monitoring was promulgated on May 4 2011. The provisions clearled definy the responsibilities of the medical institutions who are one of the main body of adverse drug reaction reporting.Combined with the provisions, this article aims to introduce how the medical institutions to do adverse drug reaction monitoring well during the new period of monitoring.

Key words: Medical institutions, Provisions for Adverse Drug Reaciton Reporting and Monitoring, adverse drug reaction monitoring