FDA Recommends Warning Label For Sanofi-Aventis (France)'s Ketek

NEW YORK/PARIS, May 19 (Reuters) - The U.S. Food and Drug Administration reviewers have linked Sanofi-Aventis SA’s antibiotic Ketek to 12 cases of liver failure, including four deaths, and is now recommending the company put a warning label on the drug, the Wall Street Journal said on Friday.

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