
The FDA has received reports of
hundreds of individuals who experienced a tendon rupture using Levaquin,
Cipro or one of the other fluoroquinolones. As a result of the inadequate
warnings currently provided, the consumer advocacy group, Public Citizen, filed
a lawsuit in January 2008 as a result of the FDA's failure to act on a petition
they filed in 2006, calling for more detailed information about the risk of Levaquin
tendon ruptures to be added to the warning label. There are more than 2,600 similar lawsuits pending against
Johnson & Johnson over tendon damage caused by Levaquin, according to a
report by Bloomberg.
Fluoroquinolones
like Levaquin and Avelox are the largest subset of quinolones, a family of
broad-spectrum antibiotics. They are used to treat a variety of bacterial
infections, including acute sinusitis, bronchitis, and pneumonia.
Fluoroquinolone use may result in other rare but severe and even
life-threatening side effects. If additional
information had been provided earlier to doctors and patients, many individuals
may have been able to prevent a tendon rupture or permanent damage by seeking
medical treatment at the first sign of pain or inflammation.
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