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- W3125895085 abstract "The scope of product liability for prescription drug injuries is a highstakes matter. As the recent Vioxx litigation illustrates, drug manufacturers can face numerous lawsuits when users are injured by risks discovered only after the drug reaches the market. The extent to which Food and Drug Administration (FDA) decisions preempt tort liability has emerged as a major issue. The agency itself has issued a policy that favors preemption when a drug manufacturer consults with the agency about a new risk. The Supreme Court has found liability preempted for medical devices based on an express preemption provisions and is expected to make an important ruling on drug preemption this term in Wyeth v. Levine . Some believe that the Court will rule in favor of preemption even though there is no express statutory provision for drugs." @default.
- W3125895085 created "2021-02-01" @default.
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- W3125895085 date "2008-12-01" @default.
- W3125895085 modified "2023-09-26" @default.
- W3125895085 title "Drug Preemption and the Need to Reform the FDA Consultation Process" @default.
- W3125895085 cites W2030881336 @default.
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- W3125895085 doi "https://doi.org/10.1177/009885880803400403" @default.
- W3125895085 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/19216247" @default.
- W3125895085 hasPublicationYear "2008" @default.
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