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Statins and Adverse Cardiovascular Events in Moderate-Risk Females: A Statistical and Legal Analysis with Implications for FDA Preemption Claims

机译:中度风险女性的他汀类药物和不良心血管事件:对FDA优先购买权主张的统计和法律分析

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摘要

This article presents: (1) meta-analyses of studies of cardioprotection of women and men by statins, including Lipitor (atorvastatin), and (2) a legal analysis of advertising promoting Lipitor as preventing heart attacks. The meta-analyses of primary prevention clinical trials show statistically significant benefits for men but not for women, and a statistically significant difference between men and women. The analyses do not support (1) statin use to reduce heart attacks in women based on extrapolation from men, or (2) approving or advertising statins as reducing heart attacks without qualification in a population that includes many women. The legal analysis raises the question of whether Lipitor’s advertisements, which omit that Lipitor’s clinical trial found slight increased risk for women, is consistent with the Food, Drug, and Cosmetics Act and related Food and Drug Administration (FDA) regulations. The analysis suggests that FDA regulation should not preempt state law actions challenging advertising that is not supported by FDA-approved labeling. Our findings suggesting inadequate regulation of the world’s best-selling drug also counsel against courts accepting the FDA’s claimed preemption of state law causes of action relating to warnings and safety. Courts evaluating preemption claims should consider actual agency performance as well as theoretical institutional competence. Billions of health-care dollars may be being wasted on statin use by women but the current regulatory regime does not create incentives to prevent such behavior.
机译:本文介绍:(1)他汀类药物(包括立普妥(atorvastatin))对男女心脏保护作用研究的荟萃分析,以及(2)宣传立普妥预防心脏病发作的广告的法律分析。一级预防临床试验的荟萃分析显示,对男性有益,但对女性无统计学意义,并且男性与女性之间存在统计学差异。这些分析不支持(1)根据男性的推断使用他汀类药物减少女性心脏病发作,或(2)批准或宣传他汀类药物减少心脏病发作而无资格在包括许多女性在内的人群中使用。法律分析提出了一个问题,即立普妥的广告是否忽略了立普妥的临床试验发现女性患病风险略有增加,该广告是否符合《食品,药品和化妆品法》以及相关的食品药品管理局(FDA)法规。分析表明,FDA法规不应抢先挑战没有获得FDA批准标签支持的广告的州法律行动。我们的调查结果表明,对全球最畅销药物的监管不充分,也为法院接受了FDA声称的先发制人的州法律与警告和安全有关的诉讼因由提供法律咨询。评估优先权要求的法院应考虑实际的代理业绩以及理论上的机构能力。妇女可能在使用他汀类药物上浪费了数十亿美元的医疗保健费用,但是当前的监管制度并未产生预防这种行为的诱因。

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