Posting date: April 28, 2004
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Health Affairs, 10.1377/hlthaff.w4.249
Copyright © 2004 by Project HOPE


Web Exclusives

Perspective: Direct-To-Consumer Advertising: Developing Evidence-Based Policy To Improve Retention And Comprehension

David L. Riggs 1, Stacy M. Holdsworth 2*, David R. McAvoy 3

1 David Riggs is a senior regulatory associate at Eli Lilly and Company in Indianapolis, Indiana.
2 Stacy Holdsworth is manager, U.S. Regulatory Affairs, Eli Lilly and Company.
3 David McAvoy is an attorney and director of the Office of Scientific and Regulatory Policy.

*Corresponding author.

  Abstract

Pharmaceutical advertising was historically directed toward health care professionals and mainly communicated through medical journals. The arrival of direct-to-consumer advertising has sparked both praise and criticism. Although current Food and Drug Administration requirements for drug promotion were written from a health care professional perspective, the same regulations have been applied to advertising directed at consumers. This has led to questions regarding the appropriate method for communicating detailed medical information. Rigorous research is needed to evaluate and determine the most effective format for communicating benefit and risk information to consumers. New standards for drug advertising to consumers should be grounded in data derived from this type of research.

Key Words: Consumer Issues, Legal/Regulatory Issues, Media, Pharmaceuticals, Ethical Issues, Health Spending


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M. F. Hollon
Direct-to-Consumer Advertising: A Haphazard Approach to Health Promotion
JAMA, April 27, 2005; 293(16): 2030 - 2033.
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