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Floxin Legal Information Center

The U.S. Food and Drug Administration (FDA) believes the fluoroquinolone antibiotic ofloxacin—sold as Floxin—might cause nerve damage and tendon injuries.

What Is Floxin and What Is It Prescribed For?

Floxin was a member of the fluoroquinolone class of antibiotics, which the FDA approved for the treatment of bronchitis, pneumonia, skin infections, urinary tract infections, some sexually transmitted diseases, and prostatitis. Floxin was first patented ofloxacin in 1982, and the FDA approved it in 1990. Johnson & Johnson sold it until 2009, and until it discontinued Floxin, it came in the form of oral tablets, injectable solutions, and topical formulations applied to the ears and eyes.

According to its label, Floxin works by inhibiting DNA synthesis in bacteria and is bacteriacidal.

Floxin Might Cause Dangerous Side Effects

According to its drug label, Floxin might cause the following adverse side effects:

  • Tendon rupture
  • Myasthenia gravis (muscle weakness)
  • Central nervous system disorders (tremors, restlessness, lightheadedness, and confusion)
  • Hypersensitivity reactions (loss of consciousness and cardiovascular collapse)
  • Life-threatening skin reactions (toxic epidermal necrolysis, Stevens-Johnson syndrome)
  • Clostridium difficile associated diarrhea (diarrhea caused by overgrowth of the bacterium C. difficile)
  • Peripheral neuropathy (pain, burning, tingling, numbness, and nerve damage)

FDA warnings associated with Floxin and other fluoroquinolone antibiotics have become more common over time. In 2008, the agency added a black box warning, the most serious type of alert, to Floxin’s label to advise the public that Floxin use is associated with tendon rupture. Patients over 60, those taking corticosteroids, and patients who have undergone a transplant are the most likely to suffer from a tendon rupture. Sometimes tendon problems can occur long after patients have ceased taking Floxin.

In August 2013, the FDA issued a drug safety communication advising the public that it was requiring a label-change to Floxin and other fluoroquinolone antibiotics to “better describe the serious side effect of peripheral neuropathy,” which can occur soon after Floxin treatment begins. It is associated with oral and injectable fluoroquinolones but not topical formulations of the drugs that are applied to the eyes and ears.

RLG’s Floxin Lawyers Will Make Things Easier

The process of demanding compensation for the harm you’ve suffered can be complicated, even if it doesn’t seem fair that you should have to go through even more trouble to be made whole again. The lawyers at the Rottenstein Law Group believe that obtaining legal satisfaction from those who harmed you shouldn’t require more hardship. That’s why we do everything we can to streamline the process, and we will file a Floxin lawsuit on your behalf if necessary. RLG will also keep you up to date on any Floxin class action lawsuits, additional FDA Floxin warnings, and Floxin FDA recall announcements. If you have taken Floxin and believe it harmed you, contact RLG today.

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