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确保消费者从药品广告中获得适当信息:美国食品药品监督管理局的作用是什么?

Ensuring that consumers receive appropriate information from drug ads: what is the FDA's role?

作者信息

Waxman Henry A

机构信息

House Committee on Government Reform, Congress, USA.

出版信息

Health Aff (Millwood). 2004 Jan-Jun;Suppl Web Exclusives:W4-256-8. doi: 10.1377/hlthaff.w4.256.

Abstract

The promise of direct-to-consumer (DTC) prescription drug advertisements lies in their potential to educate consumers about medical conditions and the possibility of treatment. But this promise can only be fulfilled if consumers are given clear and accurate information. The responsibility for ensuring that this occurs falls on the Food and Drug Administration (FDA). Recent congressional investigations have indicated that the agency is failing at this task, as FDA enforcement actions against false and misleading ads have declined precipitously in recent years. Other FDA efforts, such as its recently released guidelines on prescription drugs, do not appear to be helpful, potentially confusing consumers more than helping them.

摘要

直接面向消费者(DTC)的处方药广告的前景在于其有潜力让消费者了解医疗状况以及治疗的可能性。但只有在向消费者提供清晰准确的信息时,这一前景才能实现。确保这一点实现的责任落在了食品药品监督管理局(FDA)身上。最近的国会调查表明,该机构在这项任务上未能达标,因为近年来FDA针对虚假和误导性广告的执法行动急剧减少。FDA的其他努力,比如其最近发布的处方药指南,似乎也无济于事,可能给消费者造成的困惑多于帮助。

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