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。
Objective It discusses mainly how to perfect our ADR monitor system. Methods It applies mainly the literature method and uses the foreign successful experience. ResuJts 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.
出处
《中国药物警戒》
2010年第2期95-97,共3页
Chinese Journal of Pharmacovigilance
关键词
药品不良反应
监测
法律法规
adverse drug reaction（ADR）
monitor
law and regulation
