摘要
我国药品不良反应管理主要是依照《药品不良反应报告和监测管理办法》(以下简称《办法》),对药品不良反应进行管理包括报告、监测和控制、评价等,经过几年时间的实践,既检验出该《办法》的有效性,也反映出《办法》中缺乏时代性的不足,对此作了分析并探讨了强化管理的发展方向。
The management of the adverse side effect of drugs produced in China is based on Management of Report and Supervision of Drug Side Effect,which includes report,supervision,control and evaluation.After several years of implementation,the authors have found some drawbacks in the document.In this paper,the authors present their opinions on strengthening the management and point to the direction for development.
出处
《南京中医药大学学报（社会科学版）》
2008年第4期228-232,共5页
Journal of Nanjing University of Traditional Chinese Medicine(Social Science Edition)
关键词
药品不良反应
监管
趋势
adverse side effect of drugs
supervision
tendency
