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打击假药犯罪行为:2016 年至 2021 年 FDA 犯罪调查办公室数据库评估。

Criminal Action Against Drug Counterfeiters: Assessment of the FDA Office of Criminal Investigation Database 2016 Through 2021.

机构信息

University of Connecticut School of Pharmacy, Storrs, CT, USA.

出版信息

Ann Pharmacother. 2022 Dec;56(12):1333-1338. doi: 10.1177/10600280221092482. Epub 2022 May 2.

Abstract

OBJECTIVE

The objective of this study was to describe law enforcement oversight of counterfeit drugs by the Food and Drug Administration (FDA) in the United States from 2016 through 2021.

METHODS

The FDA Office of Criminal Investigation database with hyperlinked press releases of enforcement actions was used to identify legal action against drug counterfeiters. Incidences of counterfeit drugs sold via Internet, how often they were obtained without a prescription, the most prevalent counterfeit drugs, the countries where counterfeit operations occurred, and the scale of counterfeit operations were assessed.

RESULTS

There were 130 unique enforcement actions against counterfeiting organizations and individuals. Overall, 64.6% of enforcement actions involved counterfeit products sold over the Internet, in 84.6% of actions counterfeit medications could be obtained without a prescription, and in 33.1% of actions the products were sold as dietary supplements. Sexual dysfunction, opioid, stimulant, anabolic muscle building, benzodiazepine, and dermatologic drugs were most counterfeited. China was the most prevalent country to produce counterfeit drugs followed by India, Turkey, Pakistan, and Russia. Counterfeiting operations were large with tens of millions of pills and hundreds of millions of dollars in sales. Health outcomes for counterfeit drugs were rarely discussed in the press releases and not all press releases had data for each parameter of interest.

CONCLUSION AND RELEVANCE

This is the first report assessing enforcement actions against drug counterfeiters from the FDA Office of Criminal Investigation. The FDA is actively involved in identifying and prosecuting counterfeit drug rings, but the number of enforcement actions is smaller than the size of the problem.

摘要

目的

本研究旨在描述 2016 年至 2021 年期间美国食品和药物管理局(FDA)对假冒药品的执法监督情况。

方法

利用 FDA 刑事调查办公室的数据库及其执法行动的超链接新闻稿,确定针对假药造假者的法律行动。评估通过互联网销售的假冒药品的发生率、无处方获得的频率、最常见的假冒药品、发生假冒活动的国家以及假冒活动的规模。

结果

共有 130 项针对假冒组织和个人的单独执法行动。总体而言,64.6%的执法行动涉及通过互联网销售的假冒产品,在 84.6%的行动中可以无处方获得假冒药物,在 33.1%的行动中,这些产品被作为膳食补充剂销售。性功能障碍、阿片类药物、兴奋剂、合成代谢肌肉增强、苯二氮䓬类药物和皮肤科药物是最常被假冒的药物。中国是生产假冒药品最常见的国家,其次是印度、土耳其、巴基斯坦和俄罗斯。假冒药品的规模庞大,有上千万片药丸和数亿美元的销售额。假药的健康后果在新闻稿中很少被讨论,并不是所有的新闻稿都有每个关注参数的数据。

结论和相关性

这是第一份评估 FDA 刑事调查办公室打击假药造假者执法行动的报告。FDA 积极参与识别和起诉假药团伙,但执法行动的数量小于问题的规模。

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