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Is the FDAs expedited review process putting riskier drugs on the market?

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Is the FDAs expedited review process putting riskier drugs on the market?

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No. Vioxx received a six-month priority review because the drug potentially provided a significant therapeutic advantage over existing approved drugs due to fewer gastrointestinal side effects, including bleeding. A product undergoing a priority review is held to the same rigorous standards for safety, efficacy, and quality that FDA expects from all drugs submitted for approval.

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