Houston Personal Injury Lawyers Houston Personal Injury Lawyers Houston Personal Injury Lawyers Houston Personal Injury Lawyers Houston Personal Injury Lawyers Houston Personal Injury Lawyers

If you have been injured by someone else’s negligence, demand serious legal representation.
Read More

We know what it takes to hold the pharmaceutical companies accountable.
Read More

If you have been hurt by a medical device, demand compensation.
Read More

If you have been exposed to asbestos, we can help you fight for justice.
Read More

Don’t let an employer take advantage of you. Fight back.
Read More

Your loved ones are important to you. We can help you stand up for them.
Read More





Ketek Lawyer, Ketek Attorney

Ketek (Generic: Telithromycin)

Problems associated with the antibiotic Ketek (Generic: Telithromycin) were first reported in January of 2006 when researchers released information about three cases of severe liver problems in patients at a North Carolina hospital. After being treated with Ketek, the patients began to suffer health complications and had to be hospitalized. The liver problems aggravated by the use of Ketek claimed the life of one of the patients, prompting a Federal investigation. Federal regulators reported they were examining an unknown number of U.S. cases involving Ketek and would be consulting with overseas counterparts.

Manufactured by Sanofi-Aventis, Ketek was approved in 2004 for the treatment of acute bacterial infections from chronic bronchitis, acute bacterial sinusitis and community-acquired pneumonia. After the reports of severe liver problems in patients taking Ketek, the FDA began to examine their databases for any other reports of similar liver problems in patients who were prescribed Ketek.

It is the opinion of Dr. John Hanson, a doctor at the liver transplant center at Carolinas Medical Center, that all doctors should be alerted to a possible link between liver damage and the use of Ketek. The Carolinas Medical Center in Charlotte, N.C., also struggled to treat patients suffering from complications with Ketek. One patient died, another had to receive a liver transplant, and the third contracted drug-induced hepatitis after being treated with Ketek. Fortunately, the patient was able to recover from hepatitis after treatment of Ketek was stopped.

FDA Action

After further investigations, the FDA was able to connect twelve cases of liver failure to the use of the antibiotic Ketek. Four patients of the twelve lost their lives due to the liver problems. The FDA confronted Sanofi-Aventis, the manufacturer of Ketek, to add a warning label to the drug. Back in 2001 and 2003, the FDA refused to approve Ketek due to the lack of safety information on the label of the drug. Although it was eventually approved, the U.S. government was wary of the decision after accusations arose questioning the validity of one of the manufacturer’s tests.

Legal Help for Ketek Users

If you or a loved one has suffered from liver failure or any other side effect as a result of using Ketek, contact the attorneys of Pulaski & Middleman, LLC for a free initial consultation.

To take advantage of your free consultation, call 1-800-BAD-DRUG (1-800-223-3784) or fill out the short form found on the right.

Recent Cases

  • $2,500,000
    Former employee of a Houston gasket manufacturer. Client was only exposed during 3 summers.. (more)
  • $3,250,000
    Former Navy man who removed asbestos from ships in several Navy shipyards. Case settled during trial.
  • $3,500,000
    Former Navy man who worked at several shipyards as a machinist. (Case settled before trial.)
  • $4,000,000
    Dry wall worker, auto mechanic and a Navy man. Family has partially settled the case.. (more)