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A warning about KETEK®

The recent news linking the antibiotic KETEK® to severe liver damage has prompted the FDA to issue a warning and take a closer look at the medication’s labeling.

KETEK®, or telithromycin, was first introduced to the American market by manufacturer Sanofi-Aventis in 2004. The antibiotic is used for the treatment of bacterial infections, pneumonia, bronchitis, and bacterial sinusitis. While the drug has been widely used throughout Europe and Japan for many years, the Food and Drug Administration only recently approved the use of KETEK® in the United States in 2004.

Now, a number of patients have suffered severe liver damage as a result of the use of KETEK®. There have been three reported cases of liver toxicity; one patient needed a liver transplant and another died.

If you are taking or considering taking KETEK®, the FDA recommends:

• You be closely monitored for liver damage.
• You do not discontinue use of KETEK® before consulting with your doctor.
• You contact your doctor immediately if you are experiencing side effects such as yellowing of the skin, or blurred vision.
• You never use KETEK® to treat viral infections.

The FDA is determining whether label changes are needed.

You may be entitled to compensation for damages if you have been harmed as a result of KETEK® use.

Your best line of defense is to contact one of the lawyers at Phillips and Associates. Don’t wait until the statute of limitations has expired – you only have a limited amount of time to file your lawsuit. Contact our office today for a complimentary case evaluation.

We will defend your rights with honor and see that justice is served.