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E-cigarettes, vaping, and youth

机译:电子烟,电子烟和青春期

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摘要

The Family Smoking Prevention and Tobacco Control Act of 2009 empowered the US Food and Drug Administration (FDA) to regulate tobacco, the leading preventable cause of death. The agency, however, initially exercised authority only over specific tobacco products: cigarettes, cigarette tobacco, roll-your-own (loose tobacco), and smokeless tobacco. This decision left other forms of tobacco unregulated. Five years later, in April 2014, the FDA sought to close this regulatory gap by issuing proposed rules—referred to as "deeming"—to regulate electronic cigarettes, cigars, pipe tobacco, nicotine gels, waterpipe (hookah) tobacco, and orally ingested dissolvable tobacco products. The proposed rules represent a watershed moment in tobacco control but do not go far enough in regulating e-cigarettes, a product with uncertain benefits and potentially significant harms.
机译:2009年《家庭吸烟预防和烟草控制法》授权美国食品和药物管理局(FDA)监管烟草(可预防的主要死因)。但是,该机构最初仅对特定的烟草产品行使授权:卷烟,卷烟烟草,手卷(散装烟草)和无烟烟草。这一决定使其他形式的烟草不受管制。五年后,2014年4月,FDA试图通过发布拟议的规则(称为“视为”)来规范电子烟,雪茄,烟斗烟,尼古丁凝胶,水烟(hookah)烟草和口服摄入的食品,以缩小这一监管差距可溶性烟草制品。拟议的规则代表了烟草控制中的分水岭,但在调节电子烟方面却远远不够,这种电子烟的好处不确定,可能危害很大。

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