摘要
目的完善药品不良反应信息监管制度。方法以药品不良反应案例为切入点,分析药品不良反应信息监管中存在的问题并提出建议。结果与结论完善多级药品不良反应监测体系、完善两级信息发布制度、完善突发药品不良事件的监管机制,为政府监管和公众安全用药提供有效的信息。
Objective Improve the information monitoring system of ADR. Methods Based on the cases of ADR,analyze the problems of ADR information supervision and make recommendations. Results and Conclusion Perfect the multi-level monitoring system for ADR,the two-stage information release system and the regulatory mechanism of unexpected adverse drug events.Provide effective information for government regulation and public safety for the drug.
出处
《中国药事》
CAS
2010年第9期837-839,880,共4页
Chinese Pharmaceutical Affairs
