我院药品不良反应监测工作规范介绍

目的:规范我院药品不良反应监测工作。方法:根据《药品不良反应报告和监测管理办法》,对我院药品不良反应监测组织机构的建立和药品不良反应的发现、收集、分析、评价、反馈、整理及量化考核等制订操作规范。结果:规范的建立使药品不良反应报告数量逐年递增。结论:该规范切实可行,操作良好。

Introduction of the Adverse Drug Reaction Monitoring Work Specification in Our Hospital

OBJECTIVE:To standardize the operation of monitoring work of the adverse drug reaction in our hospital.METHODS:Based on the newly revised reporting and monitoring administration measures on adverse drug reaction,a detailed specification on a series of operations such as the finding,collection,analyzing,evaluation,feedback,sorting and quantization check of the drug adverse reaction(ADR)and the organization of the drug adverse reaction monitoring in our hospital was formulated.RESULTS:ADR reporting cases increased year by year in our hospital after the specification was formulated.CONCLUSION:This specification is feasible in operation,which can be put into practice well.