摘要
世界各国政府都面临假冒伪劣药品监管的难题,但目前对此尚无统一概念,可能不利于在全球范围内对假冒伪劣药品进行监管。本文使用了世界卫生组织推荐使用的一组术语"劣质、假造、标签不当、伪造、假冒"对假冒伪劣药品的概念进行界定,介绍了其危害及防控措施,以期为药品监管工作提供参考。
Governments around the globe are faced with the hard problem in the control of substandard/spurious/falsely labeled/falsified and counterfeit(SSFFC)medicines.However,at present,there is no unified definition on the matter,which is unfavorable to the control of SSFFC medicines globally.In this paper,we use such technical terms as SSFFC medical prod-ucts to define what used to be widely known as“counterfeit medicine”.At the same time,we also introduce the harms and con-trol measures for SSFFC drugs,so as to provide reference for drug supervision and surveillance.
作者
王蒙
叶小飞
冯红云
侯永芳
郭晓晶
贺佳
WANG Meng;YE XiaoFei;FENG HongYun;HOU YongFang;GUO XiaoJing;HE Jia(Teaching Office of Health Statistics,Faculty of Health Service,Second Military Medical University,Shanghai 200433,China;Center of Drug Evaluation,China Food and Drug Administration,Beijing 100045,China)
出处
《药学服务与研究》
CAS
2018年第2期120-122,共3页
Pharmaceutical Care and Research
基金
国家自然科学基金面上项目(81373105)
上海市第四轮公共卫生三年行动计划重点学科建设项目(15GWZK0901)
关键词
假冒伪劣药品
药事管理
药物警戒
综述
substandard,spurious falsely labelled,falsified and counterfeit medicines
pharmaceutical administration
pharmacovigilance
review
