首页> 外文期刊>The New England journal of medicine >Impossible? Outlawing state safety laws for generic drugs.
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Impossible? Outlawing state safety laws for generic drugs.

机译:不可能?禁止仿制药的国家安全法。

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摘要

In the 2009 case Wyeth v, levine, the Supreme Court ruled that manufacturers of brand-name drags could be sued under state law for failing to adequately warn of new risks discovered after the drug was approved for marketing by the Food and Drug Administration (FDA). The Court rejected Wyeth's argument that state lawsuits were preempted because federal law prohibited the manufacturer from changing the label without FDA approval. The Court held, first, that Congress did not expressly forbid states from requiring additional safety warnings on drug labels. Second, the FDA had promulgated a "changes being effected" regulation, which explicitly permitted the drug manufacturer to make labeling changes to strengthen a warning without preapproval by the FDA. Finally, the Court noted, "it has remained a central premise of federal drug regulation that the manufacturer bears responsibility for the con-tent of its label at all times [including] . . . ensuring that its warnings remain adequate as long as the drug is on the market."
机译:在2009年Wyeth诉Levine一案中,最高法院裁定,由于未能充分警告在美国食品药品监督管理局(FDA)批准该药物上市后发现的新风险,该州法律可能会起诉名牌药品制造商。 )。法院驳回了惠氏关于免于州级诉讼的论点,因为联邦法律禁止制造商在未经FDA批准的情况下更改标签。首先,法院裁定,国会没有明确禁止各州在药品标签上要求其他安全警告。其次,FDA颁布了“正在实施的变更”法规,该法规明确允许药物制造商在未经FDA事先批准的情况下进行标签更改以加强警告。最后,法院指出,“仍然是联邦毒品法规的中心前提,制造商在任何时候都要对其标签内容负责(包括……),以确保其警告在毒品使用期间一直保持适当。在市场上。”

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