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FDA Regulation of TobaccoPolitics, Law, and the Public's Health
Lawrence O. Gostin, JD
JAMA. 2009;302(13):1459-1460.
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| Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings. |
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Cigarette smoking remains the leading preventable cause of death in the United States, causing an estimated 438 000 deaths annually, including 38 000 deaths by exposure to secondhand smoke.1 However, regulating tobacco has been politically dangerous terrain, with the industry misleading the public, lobbying Congress, and portraying smoking as a personal responsibility.2 When the US Food and Drug Administration (FDA) tried to curtail the promotion and accessibility of cigarettes to children and adolescents in 1996, the US Supreme Court struck it down, reasoning that in the Food, Drug, and Cosmetic Act (FDCA), Congress intended to exclude tobacco from the FDA's jurisdiction.3
On June 22, 2009, President Obama signed the Family Smoking Prevention and Tobacco Control Act (FSPTCA), empowering the FDA to regulate tobacco.4 Although historic, advocates express concern that the bill does not go far enough and harbor suspicions about the lobbying of Philip Morris, an unlikely supporter . . . [Full Text of this Article] FDA Powers to Regulate Tobacco
Author Affiliation: ONeill Institute for National and Global Health Law, Georgetown University, Washington, DC.
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