大麻二酚导致了对COVID-19感染的未经证实的健康声明:蛇油药物的回归。

Allan Tran, Natasha Y Sheikhan, Tania Sheikhan, Dominik A Nowak, Theodore J Witek
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引用次数: 2

摘要

背景:美国食品和药物管理局(FDA)监督、检查和强制执行声称能够减轻、预防、治疗、诊断或治愈COVID-19的公司的产品推广。在大流行期间引入与covid -19相关的诊断和治疗方法,突出了严格临床试验以确保此类干预措施的安全性和有效性的重要性。本报告的目的是对针对COVID-19感染的卫生产品促销违规行为进行描述性审查。方法:在18个月内(2020年3月6日至2021年8月30日)检索FDA药物评估和研究中心发出的警告信,以确定促销违规行为。审查了被归类为“与2019冠状病毒病(COVID-19)相关的未经批准和贴错标签的产品”的FDA违规信函。对每封信进行内容分析,以确定产品类型、促销地点、违规类型和原产国的类别。对于与大麻二酚相关的违规行为,在其自己的产品类别中重复进行内容分析。结果:共报告信函130封。在所有信件中,大麻二酚产品是最常见的违规对象(15/130;11.5%)。在大麻二酚信件中,所有报告了未经批准的产品的推广(15/15;100%),品牌错误(15/15;100%),和/或声称缺乏科学依据(14/15;93.3%)。所有促销违规行为都链接到网站(15/15;100%),以及其他主流平台:Facebook、Instagram、YouTube、Twitter、LinkedIn和电子邮件。最后,大麻二酚产品被描述为通过作为抗病毒药物(5;33.3%),促炎(1;6.7%),抗炎(7;46.7%),免疫增强剂(5%;40%),免疫抑制剂(2;13.3%),及/或其他(2;13.3%)。结论:尽管迫切需要COVID-19治疗,但公司的宣传材料必须符合标准的监管要求,即证实索赔。随着疫情的持续,FDA必须继续努力监督、检查和强制执行违规公司。大麻二酚相关物质在未经证实的治疗COVID-19感染的产品中名列前茅。提高公众、医疗保健提供者和利益相关者的认识,突出药物批准流程的价值,同时保护公共安全。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Unsubstantiated health claims for COVID-19 infections are led by cannabidiol: return of snake oil medicine.

Unsubstantiated health claims for COVID-19 infections are led by cannabidiol: return of snake oil medicine.

Background: The United States Food and Drug Administration (FDA) monitors, inspects, and enforces the promotion of products by companies that claim to mitigate, prevent, treat, diagnose, or cure COVID-19. The introduction of COVID-19-related diagnostics and therapeutics during the pandemic has highlighted the significance of rigorous clinical trials to ensure safety and efficacy of such interventions. The objective of this report is to provide a descriptive review of promotional violations of health products for COVID-19 infection.

Methods: Warning letters issued by the FDA's Center for Drug Evaluation and Research were retrieved over an 18 month period (March 6, 2020, to August 30, 2021) to identify promotional violations. FDA violation letters categorized as "Unapproved and Misbranded Products Related to Coronavirus Disease 2019 (COVID-19)" were reviewed. A content analysis was performed for each letter to identify categories for product type, promotional venue, violation type, and country of origin. For cannabidiol-related violations, a content analysis was repeated within its own product category.

Results: A total of 130 letters were reported. Across all letters, cannabidiol products were the most frequent subject of violation (15/130; 11.5%). Of the cannabidiol letters, all reported the promotion of unapproved products (15/15; 100%), misbranding (15/15; 100%), and/or had claims that lacked scientific substantiation (14/15; 93.3%). All promotional violations were linked to websites (15/15; 100%), along with other mainstream venues: Facebook, Instagram, YouTube, Twitter, LinkedIn, and email. Lastly, the cannabidiol products were described to provide therapeutic benefit to COVID-19, by acting as an anti-viral (5; 33.3%), pro-inflammatory (1; 6.7%), anti-inflammatory (7; 46.7%), immune-booster (5; 40%), immune-suppressor (2; 13.3%), and/or other (2; 13.3%).

Conclusion: Despite the urgent need for COVID-19 treatments, promotional material by companies must comply with standard regulatory requirements, namely substantiation of claims. As the pandemic persists, the FDA must continue their efforts to monitor, inspect, and enforce violative companies. Cannabidiol-related substances led the spectrum of products with unsubstantiated claims to treat COVID-19 infection. Improving awareness among the public, healthcare providers, and stakeholders highlights the value of drug approval process, while protecting public safety.

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