中国药物警戒 ›› 2010, Vol. 7 ›› Issue (2): 95-97.

• 管理研究 • 上一篇    下一篇

如何完善我国药品不良反应监测体系

郭莹, 王胜兴   

  1. 沈阳药科大学工商管理学院,辽宁 沈阳 110016
  • 收稿日期:2016-02-19 修回日期:2016-02-19 出版日期:2010-02-08 发布日期:2016-02-19
  • 作者简介:郭莹,女, 讲师,药剂学与药事管理。

Perfection of Adverse Drug Reaction Monitoring System in China

GUO Ying, WANG Sheng-xing   

  1. College of Business Administration, Shenyang Pharmaceutical University, Liaoning Shenyang 110016, China
  • Received:2016-02-19 Revised:2016-02-19 Online:2010-02-08 Published:2016-02-19

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摘要： 目的 探讨如何使我国药品不良反应监测体系更加完善。方法 主要采用文献查阅法和借鉴国外的成功经验。结果 与结论 通过完善相关法律法规、药品不良反应报告制度、药品不良反应监测体系、中药不良反应监测制度等多个环节的措施来完善我国药品不良反应监测规制。

关键词: 药品不良反应, 监测, 法律法规

Abstract: Objective It discusses mainly how to perfect our ADR monitor system. Methods It applies mainly the literature method and uses the foreign successful experience. Results and Conclusion By perfecting the relative law and regulation, ADR report system, ADR monitor system, the ADR of tradional Chinese medicine monitoring system, all of these Methods will help to perfect our ADR monitor system.

Key words: adverse drug reaction(ADR), monitor, law and regulation

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