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[假冒伪劣药品概述]

[Counterfeit and Falsified Drugs: an Overview].

作者信息

Taverriti-Fortier Corine, Pape Elise, Scala-Bertola Julien, Tréchot Philippe, Maincent Philippe, Gibaja Valérie, Gambier Nicolas

机构信息

CHU Nancy, Laboratoire de Pharmacologie Clinique et Toxicologie, Nancy, France.

CHU Nancy, Laboratoire de Pharmacologie Clinique et Toxicologie, Nancy, France - CHU Nancy, Centre Régional de Pharmacovigilance de Lorraine, Nancy, France - Université de Lorraine, UMR CNRS 7365 IMoPA, Vandoeuvre-lès-Nancy, France.

出版信息

Therapie. 2015 Sep-Oct;70(5):455-64. doi: 10.2515/therapie/2015031. Epub 2015 Jun 12.

Abstract

If the traffic of fake medicines may represent an economic threat for the pharmaceutical industry, it can also be responsible of safety concerns for patients. Despite fake drugs represent a real threat for public health, the intended punishments are until now only based on intellectual property rights. Estimated to generate more than 55 billion euros per year, the traffic of falsified drugs varies from a country to another one. Indeed, the proportion of falsified drugs ranges from 1% in industrialized countries with a regulated and controlled distribution system to 60% of medicines in some developing countries. Currently, the measures developed to limit this traffic concern five main areas: legislation / regulation, cooperation, enforcement, technology and communication. Communication actions should be performed to inform health professionals as the populations about the risks of using drugs purchased outside the legal drug market.

摘要

如果假药交易对制药行业构成经济威胁,那么它也可能引发患者的安全担忧。尽管假药对公众健康构成了切实威胁,但目前预期的处罚仅基于知识产权。假药交易估计每年产生超过550亿欧元的收益,各国情况各不相同。事实上,假药比例在拥有规范和受控分销系统的工业化国家为1%,而在一些发展中国家药品中这一比例高达60%。目前,为限制这种交易而采取的措施主要涉及五个领域:立法/监管、合作、执法、技术和沟通。应开展沟通行动,向医疗专业人员以及民众宣传使用在合法药品市场以外购买的药品所带来的风险。

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