摘要
通过对影响个例药品不良反应报告评价诸如不良反应报告填写的完善程度、我国现有药品不良反应报告评价方法的局限性、联合用药、药品说明书、工作者医药学相关知识素质以及个体因素等多方面因素做一系统分析,旨在对个例药品不良反应报告评价时尽量减少干预因素的影响,以提高评价的准确性。同时对个例药品不良反应评价的重要性及其与药物警戒的关系做一简要阐述。
Systematically analyzed multiple factors of defects that affect the evaluation report for individual adverse drug reactions（ADR） in our work ,such as the degree of perfection of ADR reports, evaluation method, drug com- bination, product instructions, medical and pharmaceutical-related capability of ADR workers as well as individual factors and etc. We aimed to reduce the interference factors and increase the accuracy during the process of analysis and evaluation of ADR report. Furthermore, we have briefly described the importance of evaluation for individual ADR report and the relationship between ADR and drug safety warning.
出处
《中国药物警戒》
2012年第9期553-555,共3页
Chinese Journal of Pharmacovigilance
关键词
药品不良反应
报告评价
药物警戒
adverse drug reaction
report evaluation
pharmacovigilance
