Antibiotic: Avelox Linked to Tendn Rupture

The Potent Antibiotic Avelox Has Been Tied to Painful Tendon Ruptures, Other Injuries

Avelox (moxifloxacin hydrochloride) is a powerful, prescription antibiotic made by Bayer that has been linked to an increased risk of tendon ruptures, tendonitis, and other serious injuries. Avelox, a member of the group of drugs called fluoroquinolones, is used to treat acute bacterial sinusitis, acute exacerbations of chronic bronchitis, and community-acquired pneumonia as well as skin and skin structure infections and intra-abdominal infections caused by certain bacteria.

Tendons can rupture quickly, within hours of taking Avelox, or the injury may take weeks to develop. In some cases, patients feel pain and notice swelling or bruising in the area of the tendon, but some patients report seeing no symptoms of problems before they are injured.

People who have been injured by Avelox may have legal rights. They may be eligible to be financially compensated for medical bills, pain and suffering, lost wages, and other damages. To contact Mark & Associates, P.C. today for a free legal consultation and evaluation of your possible case, complete the case submission form on this page or call 1-866-50-RIGHTS (1-866-507-4448).

Common Injuries

People taking Avelox have experienced painful tendon ruptures and tendonitis, particularly in the rotator cuff in the shoulder, the hand, and the Achilles’ tendon in the foot. Tendons are cords of tissue that join muscles and bones and are essential in movement. Some Avelox injuries require extensive surgery to repair the tendon. Shortness of breath, difficulty swallowing, and swelling of the neck and face are other common injuries associated with Avelox. In some cases, patients have died after taking Avelox.

FDA Warns Users

The Food and Drug Administration in July 2008 ordered that a prominent “Black Box” warning be placed on the packaging of Avelox and other types of flurorquinolones to warn users and medical professionals about the risk of tendon ruptures and tendonitis. Hundreds of patients had reported such injuries, prompting the agency to take action.

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