What is Ketek?
KetekŪ is a prescription antibiotic drug made by Aventis Pharmaceuticals and known generically as telithromycin. Ketek is in a class of drugs called ketolide antibiotics, and is used to treat bacterial infections in the lungs and sinuses. Ketek has been associated with adverse side effects such as liver damage, liver disease, liver failure, and hepatitis.
All content by attorney Tom Lamb
- Ketek Label Will Get Black Box Warning and Medication Guide for Patients
On February 12, 2007 the FDA issued a news bulletin to inform the public that Sanofi-Aventis SA's antibiotic Ketek (telithromycin) is to be prescribed only for community-acquired pneumonia, and that Ketek should no longer be prescribed for two lesser medical conditions, acute bacterial exacerbation of chronic bronchitis and acute bacterial sinusitis.
- FDA Advisory Panel Suggests "Black Box" Warning For Ketek and More Restricted Use
- Sanofi-Aventis Antibiotic Ketek: Serious Side Effects Outweigh Benefits For Bronchitis and Sinusitis. While this FDA advisory panel did not recommend a Ketek recall, according to a December 13, 2006 report about Ketek by CBS News, there is a new Congressional probe under way to determine whether Ketek should remain on the market.
- New Warning for Ketek in Canada Concerns Possible Serious Liver Problems
- September 2006 "Dear Doctor" letter warns about hepatotoxicity risks including: hepatitis, liver disease, and liver failure. Acute liver failure . . . leading to liver transplant or death have been observed during or immediately after the completion of Ketek treatment.
- FDA Drug Safety Office Wants Black Box Warning For Ketek Liver Problems
- In mid-May 2006 the FDA's drug safety office recommended that a black box warning be added to the Ketek label, stating that "severe, life-threatening, and in some cases fatal" liver toxicity has been reported in patients taking Ketek. The recommendation came after FDA safety reviewers found that the antibiotic Ketek has been linked to 12 cases of liver failure, including four deaths, in the U.S.
- Reports of Liver Problems Associated With Antibiotic Ketek Prompt Warnings
- On January 20, 2006 the Annals of Internal Medicine made available online an "early" release version of a report that described three cases of liver problems associated with the antibiotic Ketek (telithromycin). The three cases described in the report involved patients at Carolinas Medical Center, in Charlotte, North Carolina, who developed serious liver problems after taking Ketek.
- What is Ketek and Why is the FDA Warning About Liver Problems
- The FDA issued a warning about Ketek following an article in the Annals of Internal Medicine that described three cases of severe liver toxicity, including one death, in patients using Ketek.
- Ketek Class Actions
- We believe an individual lawsuit is a better way to handle an adverse drug reaction or other injury or death caused by Ketek.
- Ketek and Legal Compensation
- How to get legal compensation for an injury or death resulting from an adverse reaction to Ketek.
- Ketek Case Evaluation
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