Some of these claimed adverse side-effects include: tendonitis, tendon rupture, Achilles tendon rupture, rotator cuff (shoulder) ruptures and other tendon disorders. These injuries may be identified by swelling, bruising and pain at the site.

Initially, Public Citizen and the Illinois Attorney General requested the FDA to change labeling for Levaquin and warn of these potential harmful effects. However, the process was delayed until July 8, 2008, when the FDA finally issued a "black box warning" for Levaquin and notified health care professionals of the importance of distributing a medication guide when dispensing this medication.

Due to the delay in warning, numerous cases have arisen from patients suffering from Levaquin's side effects. This drug, still widely prescribed by many healthcare professionals, produces a risk of injury that is rather common. Levaquin has not yet been recalled, and therefore leaves healthcare professionals with the responsibility to monitor their patients and warn them of the harmful and potentially devastating effects.

If you believe you have suffered tendon damage or other side-effects from taking Levaquin, call us and ask to speak with an attorney who has experience with Levaqiun lawsuits. You may qualify for a free evaluation: 732.855.6154