中国药物警戒 ›› 2012, Vol. 9 ›› Issue (9): 553-554.

• 药械安全性研究 • 上一篇    下一篇

影响个例药品不良反应报告评价的因素

赵世丹, 鲁仲平   

  1. 黑龙江省药品不良反应监测中心,黑龙江 哈尔滨 150076
  • 收稿日期:2012-04-12 出版日期:2012-09-10 发布日期:2015-08-07
  • 作者简介:赵世丹,男,硕士研究生,主治医师,药品不良反应监测。

Factors Affecting the Evaluation of Individual ADR Reports

ZHAO Shi-dan, LU Zhong-ping   

  1. Heilongjinag Center for ADR Monitoring, Heilongjiang Haerbin 150076, China
  • Received:2012-04-12 Online:2012-09-10 Published:2015-08-07

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。

关键词: 药品不良反应, 报告评价, 药物警戒

Abstract: 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 combination, 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.

Key words: adverse drug reaction, report evaluation, pharmacovigilance