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Calcagno & Associates
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Phone: 1-800-WE-FIGHT
(718) 568-3585
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Phone: (800) 933-4448
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Levaquin (levofloxacin), a popular brand of antibiotic made by Ortho-McNeil-Janssen Pharmaceuticals, Inc., has been blamed for an increased risk of tendon ruptures, tendinitis, and other injuries in patients taking the drug. Anyone who has taken Levaquin, even for brief periods of time, is potentially at risk.
This drug is most commonly prescribed for the treatment of respiratory infections. The most common injuries reported by Levaquin users are tendon ruptures and tendonitis, particularly in the rotator cuff in the shoulder, the hand, and the Achilles’ tendon in the foot. Some injuries require extensive surgery to repair the tendon. Shortness of breath, difficulty swallowing, and swelling of the neck and face have also been reported.
In June 2008, after receiving and investigating hundreds of reports of tendon ruptures and tendonitis in patients taking Levaquin, the Food and Drug Administration ordered prominent “Black Box” warnings to be added to the product’s packaging to alert users and physicians of the increased risk of injuries. The warnings are the most severe notice the FDA can order manufacturers to place on a product’s packaging.
Levaquin users may also experience one or more of the following injuries:
If you or a loved one was prescribed the antibiotic Levaquin and suffered a ruptured tendon or other injury, contact our attorneys immediately for a free Levaquin legal consultation. Our law firm is available 24/7 to answer any Levaquin questions you may have. Contact us today for a free, no obligation, legal consultation by completing the Levaquin case evaluation form on the right side of this page or by calling 1-800-WE-FIGHT (1-800-933-4448).
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