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FDA & Ketek
An FDA safety review indicates there have been 35 Adverse Event Reports of serious liver toxicity associated with Ketek®. 12 involved liver failure, as well as 4 deaths and 23 serious liver injuries. Additional FDA reports associated liver problems with Ketek®. In May 2006, it was suggested that a black box warning (the most serious type of warning) be added to the Ketek® label.
If you or a loved one has used Ketek and developed liver problems, please contact us by filling out the form below.
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