Ketek is a powerful antibiotic used to treat serious bacterial infections such
as pneumonia, sinusitis, and chronic bronchitis in adults. Manufactured by Sanofi-Aventis,
Ketek first received approval from the Food and Drug Administration in April
2004. However, in the January 2006 issue of the Annals of Internal Medicine,
there are reports of Ketek being linked to severe, potentially fatal, liver
damage including liver failure and death.
Ketek has been linked to 23 cases of severe liver injury, 12 cases of complete
liver failure, and 44 instances of other liver problems. Of the 12 cases of
liver failure, four patients died and one required a liver transplant. In addition
to acute liver damage, other adverse side effects include blurred vision, loss
of consciousness, heart arrhythmia and other irregularities and colon inflammation.
The FDA has recently urged Sanofi-Aventis to include a heightened warning on
the drug's label. The revised Ketek warning label will include the increased
risk of life-threatening liver disease and other negative effects on liver functioning.
Drug manufacturers like Sanofi-Aventis have a duty to inform the medical community
and the public about dangers associated with their drugs. Individuals who have
suffered serious injury as a result of taking Ketek may be able to hold Sanofi-Aventis
liable for their losses.
If you or someone you love been injured by taking Ketek, please contact our
service today. We can put you in touch with caring and experienced Ketek attorneys
who can evaluate your case and help you determine a course of action.
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