Pharmaceutical Advertising to Consumers: Corporate Profits vs. Public Safety

IF 0.4 Q4 ETHICS BUSINESS & PROFESSIONAL ETHICS JOURNAL Pub Date : 2005-11-01 DOI:10.5840/BPEJ200524324
P. Lansing, Michael Fricke
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Abstract

In 1997, the United States Food and Drug Administration (FDA) restated its position on direct-to-consumer advertising of pharmaceutical products, for the first time allowing the broad marketing of prescription drugs through media such as television. In 2003, pharmaceutical companies spent an estimated $3.2 billion on advertising campaigns targeting American con sumers.1 In just six short years, the pharmaceutical advertising industry shifted from being virtually nonexistent to become the tenth largest adver tising category in the United States.2 For the companies footing the bill for these advertisements, however, this money needs to be recouped through higher and higher sales revenues. Add to this the average $800 million it costs to bring a new drug to market, and pharmaceutical companies find themselves under intense pressure to produce the latest and greatest "blockbuster" drug simply to cover their enormous R&D and marketing costs.3 The pharmaceutical industry and other proponents of direct-to consumer advertising claim that the FDA's loosening of its restrictions in 1997 has produced a more informed public and saved countless lives through early disease detection and prevention, even though some industry analysts point to less altruistic motives, such as immense pressure from drug makers who could see the money to be made with television advertising.4
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面向消费者的医药广告:企业利润vs.公共安全
1997年,美国食品和药物管理局(FDA)重申了其对药品直接面向消费者广告的立场,首次允许通过电视等媒体广泛销售处方药。2003年,制药公司在针对美国消费者的广告活动上花费了大约32亿美元在短短6年的时间里,医药广告行业从几乎不存在变成了美国第十大广告类别。2然而,对于为这些广告买单的公司来说,这笔钱需要通过越来越高的销售收入来收回。再加上将一种新药推向市场的平均成本为8亿美元,制药公司发现自己承受着巨大的压力,必须生产最新、最好的“重磅炸弹”药物,仅仅是为了支付巨大的研发和营销成本制药业和其他直接面向消费者的广告的支持者声称,FDA在1997年放宽了限制,使公众更加了解情况,并通过早期疾病检测和预防挽救了无数人的生命,尽管一些行业分析人士指出了一些不那么无私的动机,比如来自制药商的巨大压力,他们看到了电视广告可以赚钱
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