medication side effects - harmful drug litigation - mass tort lawsuits
Ennis & Ennis, P.A. is also currently handling lawsuits for the following drugs: Accutane, Actiq, Adderall, Avandia, Bextra, Celebrex, Fosamax, Ketek, Ortho Evra Birth Control Patch, Paxil, Plavix, Serevent, Seroquel, Tequin, Trasylol, Viagra, Vioxx, Zelnorm & Zyprexa.
 
Ketek Lawsuit
Ketek News
Offices
Ennis & Ennis, P.A. is representing individuals that have been harmed as a result of Ketek side effects. If you or a loved one have suffered from kidney problems, heart attack, or a stroke as a result of Ketek use you may be entitled to compensation. Click here to contact one of our Ketek Attorneys about a Ketek lawsuit today.


Ketek No Longer Approved in Canada for Treatment of Bronchitis, Sinusitis or Tonsillitis/Pharyngitis

- Doctor's Guide

09/05/2007 - Upon review of the available safety information, including reported cases of severe liver injury, Health Canada has determined that the benefit-risk profile for Ketek® (telithromycin) no longer supports its use for the treatment of acute exacerbation of chronic bronchitis (AECB), acute bacterial sinusitis (ABS) or tonsillitis/pharyngitis. These indications will be removed from the label.

Ketek® continues to be indicated only for the treatment of community-acquired pneumonia (CAP) of mild to moderate severity due to Streptococcus pneumoniae, (including multi-drug resistant isolates [MDRSP]), Haemophilus influenzae, Moraxella catarrhalis, Chlamydophila (Chlamydia) pneumoniae, Legionella pneumophila, Mycoplasma pneumoniae, and Staphylococcus aureus for patients 18 years old and older.

Complete product information will be available in a revised version of the official Canadian Product Monograph. Revisions will include new contraindications against the use of Ketek® for patients with myasthenia gravis, or with a history of hepatitis and/or jaundice associated with any macrolide antibiotic. Labelling will also be strengthened regarding hepatotoxicity, visual disturbances and loss of consciousness.

The revised Product Monograph will be posted at www.sanofi-aventis.ca as soon as it is available.

Managing marketed health product-related adverse reactions depends on health care professionals and consumers reporting them. Reporting rates determined on the basis of spontaneously reported post-marketing adverse reactions are generally presumed to underestimate the risks associated with health product treatments. Any case of serious hepatic events, exacerbations of myasthenia gravis, visual disturbances, syncope or other serious or unexpected adverse reactions in patients receiving Ketek® should be reported to sanofi-aventis Canada Inc.


 

If you or a loved one have experienced liver damage, liver failure, or Stevens Johnson Syndrome as a result of Ketek side effects contact the Ketek attorneys of Ennis & Ennis today for a free confidential case evaluation. Our on staff nurse and attorneys are standing by to answer any questions you may have regarding Ketek side effects, a possible Ketek class action lawsuit, or any other type of Ketek litigation.

Washington DC Office
1101 Pennsylvania Ave.
Suite 600
Washington DC 20004
Telephone: 202-756-2972

Miami Office
1111 Brickell Avenue
11th Floor
Miami, FL 33131
Telephone: 305-913-7199

Fort Lauderdale Office
110 E. Broward Blvd.
Suite 1700
Fort Lauderdale, FL 33301
Telephone: 954-315-3934
Facsimile: 954-315-3914

 


Free Case Evaluation. Nationwide: 1-800-856-6405