S-A's Ketek under investigation by FDA over liver safety
French drug major Sanofi-Aventis' novel antibiotic Ketek (telithromycin) is under intestigation by the US Food and Drug Administration after reports of liver toxicity from patients on the drug, according to the Associated Press. A few months ago, the US drug regulator revised the agent's label, warning that rare cases of acute hepatic failure had been observed in those taking the first-in-class ketolide antibiotic (Marketletter July 10.)
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