March 28, 2000 - FDA opens probe into Warner-Lambert's Rezulin adverse events, reports FDA Webview

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The Food and Drug Administration (FDA) has open an investigation into allegations that toxicity data for the drug Rezulin and Avandia were manipulated to keep liver toxicity reports lower than they actually were. In response, the manfacture of Rezuline, Warner-Lambert has raised claims against the FDA over regulatory marketing practices, the fast-track review process, and other complaints about alleged FDA violations within the Code of Ethics for Government Service.

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