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Levaquin Injury Lawyers

Keywords: Levaquin | Tendon | Ruptures | Lawyer | Damage  | Attorney

The lawyers and attorneys at our firm are currently offering free case evaluations to victims of tendon ruptures and peripheral neuropathy associated with use of the antibiotic Levaquin.  If you or a loved one suffered from one of these Levaquin side effects, we urge you to contact our Levaquin injury lawyers as soon as possible.

Levaquin was approved by the Food and Drug Administration (FDA) in 1996.  Levaquin is a member of the fluoroquinolone family of antibiotics and is prescribed to treat bacterial infections of the lungs, urinary tract and skin. Levaquin is available by prescription only and is manufactured by Ortho-McNeil Pharmaceuticals.

Levaquin and Tendon Ruptures

Our Levaquin injury lawyers are currently representing people who suffered tendon ruptures following treatment with Levaquin.   In July 2008, the FDA finally directed the makers of Levaquin and other fluoroquinolone antibiotics to add a black box warning to their labels regarding their association with tendon damage. The FDA's move came months after the advocacy group Public Citizen sued the agency in an attempt to force it to improve safety warnings for fluoroquinolones.  At the time, Public Citizen said that the FDA had received more than 300 reports of tendon ruptures linked to these antibiotics. About 61 percent of those reports involved Levaquin.  The Levaquin injury lawyers at our firm believe that had Ortho-McNeil acted earlier to warn of this side effect,  many Levaquin users would have been spared a great deal of suffering.

 

According to the FDA, pain, swelling, inflammation, and tears of tendons including the Achilles, shoulder, hand, or others can happen in patients taking fluoroquinolone antibiotics, including Levaquin.  The FDA said the chance of experiencing tendon problems is higher in patients who are over 60 years of age, taking  steroids (corticosteroids), or who have undergone a kidney, heart, or lung transplants.

 

A warning about the increased risk of tendinitis and tendon rupture in patients taking fluoroquinolones was previously added to the prescribing information for all of these drugs, including Levaquin.  However, the FDA said it decided to add the more serious black box warning after an evaluation of the medical literature and the post-marketing adverse event reports submitted to the Adverse Events Reporting System (AERS) confirmed that serious reports of tendinitis and tendon rupture with antibiotics like Levaquin continue to be reported in similar or increased numbers. 

 

The FDA said that tendinitis and tendon rupture  associated with Levaquin and similar antibiotics most frequently involves the Achilles tendon, and rupture of the Achilles tendon may require surgical repair.  Tendinitis and tendon rupture in the rotator cuff (the shoulder), the hand, the biceps, and the thumb have also been reported. Tendon rupture can occur during or after completion of a course of Levaquin; although cases occurring up to several months after completion of therapy have been reported.

 

The FDA has warned patients taking Levaquin to stop taking the drug if they experience any symptoms of tendon rupture including a snap or pop in a tendon area; bruising right after an injury in a tendon area; or the inability to move the affected area or bear weight. Patients taking Levaquin should also discontinue the drug and call their doctor  at the first sign of pain, swelling, or inflammation in a tendon area.   They should also avoid exercise and use of the affected area.

 

Levaquin and Peripheral Neuropathy

The Levaquin injury lawyers at our firm are also representing people who developed irreversible peripheral neuropathy following treatment with Levaquin.  Peripheral neuropathy describes damage to the peripheral nervous system, the vast communications network that transmits information from the brain and spinal cord (the central nervous system) to every other part of the body.

 

People with peripheral neuropathy may experience temporary numbness, tingling, and pricking sensations (paresthesia), sensitivity to touch, or muscle weakness. Others may suffer more extreme symptoms, including burning pain (especially at night), muscle wasting, paralysis, or organ or gland dysfunction. In the most extreme cases, breathing may become difficult or organ failure may occur.

 

Peripheral neuropathy can become irreversible.  For that reason, Levaquin should be discontinued if a patient experiences symptoms of neuropathy including pain, burning, tingling, numbness, and/or weakness or other alterations of sensation including light touch, pain, temperature, position sense, and vibratory sensation.
 

Legal Help for Victims of Levaquin Side Effects

If you or a loved one suffered from a tendon rupture or peripheral neuropathy while taking Levaquin, you have valuable legal rights.  Please fill out our online form or call 1-800-LAW-INFO (1-800-529-4636) to speak with an experienced Levaquin injury lawyer.

LevaquinRSS Feed

FDA To Seek Black-Box Warning On Cipro and Levaquin

Jul 8, 2008 | Parker Waichman Alonso LLP
The U.S. Food and Drug Administration (FDA) has announced that it will seek to add black box warnings about the risk of tendon rupture associated with Cipro and Levaquin.  The drugs are in a class of antibiotics used to treat bacterial infections and black box warnings are the strongest warning the FDA issues.  Cipro is made by Bayer AG and Johnson & Johnson makes Levaquin.  Six months ago, the consumer group Public Citizen sued the FDA to require it to add black-box warnings...

Antibiotic Lawsuit Seeks Stronger Warnings on Cipro, Levaquin and Others for Tendon Damage

Jan 4, 2008 | Parker Waichman Alonso LLP
Cipro, Levaquin and other antibiotics known as fluoroquinolones have long been known to cause serious side effect, including tendon damage.  Yet despite massive amounts of evidence, the Food & Drug Administration (FDA) has not required the makers of Cipro, Levaquin and other fluoroquinolone antibiotics to add warning labels about their links to ruptured tendons and other tendon problems.  Now, the consumer advocacy group Public Citizen is trying to force the FDA to act, and has...

Despite Side Effects, Antibiotics Being Tested For Children

Aug 15, 2004 | Cox News Service
Companies that produce a group of powerful antibiotics are being encouraged by the federal government to move into the pediatrics market, even though the drugs' use for children has been discouraged for a decade because of severe side effects.The Food and Drug Administration in March approved the use of ciprofloxacin, or Cipro, for some kidney and urinary tract infections in children under 18, in the event other antibiotics failed to work.And two clinical trials are under way to demonstrate...

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