我院药品不良反应/事件报告质量分析  

Quality Analysis on ADR/ADE Reports in Our Hospital

作　　者：郑红毅[1] 周霞[1] 易太友 

机构地区：[1]四川省建筑医院,四川成都610081

出　　处：《中国执业药师》2011年第5期10-12,共3页China Licensed Pharmacist

摘　　要：目的:提高药品不良反应/事件(ADR/ADE)报告质量。方法:对我院200例ADR/ADE报告质量进行回顾性分析。结果与结论:我院ADR/ADE报告中4级报告占全部报告的26%,ADR/ADE发生的过程和处理结果项描述简单。应对医务人员和患者加强ADR/ADE的教育,提高ADR/ADE的报告水平。Objective：To improve the quality about ADRs/ADEs report in our hospital. Methods：200 reports on ADRs/ADEs in our hospital were retrospective analyzed. Results and Conclusion：Only 26% of the reports reached to the 4th Grade. The descriptions for the happening process and the handling results of ADRs/ADEs were too simple. The educations of medical workers and patients on ADRs/ADEs should be strengthened so as to improve the level of ADRs/ADEs report.

关 键 词：药品不良反应/事件 报告质量 

分 类 号：R961[医药卫生—药理学]