摘要
目的在医疗机构内部提高药品不良反应监测质量。方法从制度建设、上报平台建设、监测哨点设置、分析评价、宣传培训等环节出发,建立并实际运行药品不良反应/事件监测平台。结果通过设置6个药品不良反应监测哨点,采取3种不同上报方式,并定期进行分析评价,采取不同宣传方式进行培训宣传,建立了完善的药品不良反应监测制度。结论该平台运行良好,能准确、快速、方便地收集、分析、评价药品不良反应/事件,值得推广。
Objective To improve the quality of adverse drug reaction(ADR) monitoring in medical institutions. Methods The ADR monitoring platform was constructed by the system construction,reporting platform construction,monitoring post setting,analysis and evalu- ation, advocacy training and other aspects. Results A sound ADR monitoring system was set up by establishing 6 ADR monitoring points, taking 3 different reporting methods, conducting regular analysis and evaluation, and using different ways of publicity for training. Conclusion The platform runs well, can accurately, quickly and easily collect, analyze, evaluate adverse drug reaction/event, which is worthy of promotion.
出处
《中国药业》
CAS
2016年第16期85-87,共3页
China Pharmaceuticals
关键词
药品不良反应
药品不良事件
平台建设
哨点设置
adverse drug reaction
adverse drug event
platform construction
monitoring point