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Article

A Case for Tobacco Content Regulation by The U.S. Food and Drug Administration

Philosophy Department, University of Cape Town, Private Bag X3, Rondebosch 7701, South Africa
Curr. Oncol. 2010, 17(4), 59-61; https://doi.org/10.3747/co.v17i4.552
Submission received: 2 May 2010 / Revised: 9 June 2010 / Accepted: 5 July 2010 / Published: 1 August 2010

Abstract

Although many people welcome the recent move by the United States to give its Food and Drug Administration (FDA) the authority to regulate the content of tobacco, some worry that such regulation constitutes unwarranted interference with the freedom of competent adult tobacco consumers. The concern for protecting the autonomy of individuals is valuable indeed, but given the highly addictive nature of tobacco products (and especially the nicotine in tobacco products), the continued use of tobacco by smokers cannot —without straining credulity—be said to be autonomous. This fact, combined with a proper construal of the fda’s role and an appreciation of the substantial morbidity and mortality associated with tobacco use, makes a strong case for content regulation.
Keywords: tobacco; nicotine; FDA; autonomy; bioethics tobacco; nicotine; FDA; autonomy; bioethics

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MDPI and ACS Style

du Toit, J.A. A Case for Tobacco Content Regulation by The U.S. Food and Drug Administration. Curr. Oncol. 2010, 17, 59-61. https://doi.org/10.3747/co.v17i4.552

AMA Style

du Toit JA. A Case for Tobacco Content Regulation by The U.S. Food and Drug Administration. Current Oncology. 2010; 17(4):59-61. https://doi.org/10.3747/co.v17i4.552

Chicago/Turabian Style

du Toit, J.A. 2010. "A Case for Tobacco Content Regulation by The U.S. Food and Drug Administration" Current Oncology 17, no. 4: 59-61. https://doi.org/10.3747/co.v17i4.552

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