Thursday, October 13, 2011

Levaquin MDL Status Covered in New Conference


There are currently more than 2,500 lawsuits that have been filed on behalf of individuals throughout the United States who suffered a Levaquin tendon rupture. Of those cases, more than 1512 are pending in New Jersey state court and about 1000 are pending in federal court, where the litigation has been centralized for pretrial preceedings as part of an MDL, or multidistrict litigation, in the U.S. District Court for the District of Minnesota before U.S. District Judge John Tunheim. A recent conference in Minnesota was held to review many subjects pertaining to Levaquin litigation. According to a prior Wall Street Journal report, one of the latest Levaquin lawsuits filed in a New Jersey state court on behalf of three plaintiffs from around the U.S. charged
that Johnson & Johnson and Ortho-McNeil represented Levaquin as a safe antibiotic despite its known association with tendon damage.
The conference in Minnesota went over issues such as the number of pending cases and anticipated cases. So far, over 1,300 cases have been filed in New Jersey and over 1,800 in Illinois by patients suffering from Levaquin side effects. Another issue that was gone over was the confirmation of the date of the first New Jersey trial set to go forward on August 29th of this year.  Lawsuits, which were recently reported as having begun to circulate through the courts, allege that Levaquin has caused Achilles’ tendon ruptures and other damage. Just over a year ago, federal regulators ordered that Levaquin and similar antibiotics bear Black Box warnings about their association with serious tendon injuries.
Levaquin (levofloxacin) is an antibiotic which is prescribed to prevent bacteria from rapidly reproducing, causing infection.  It is part of a class of antibiotics known as fluoroquinolones.  Although many of the reported cases of tendon ruptures have been associated with the use of Levaquin, the side effects have also been seen with the use of other antibiotics which are part of this class, including Cipro. The FDA has received reports of at least 336 individuals who experienced a tendon rupture after using Cipro, Levaquin or one of the fluoroquinolone antibiotics. The most common tendon rupture involved the Achilles tendon. In addition, hundreds of other people have experienced tendonitis and other tendon disorders.
                                                                                                                               

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