Dallas Dangerous Drug Attorney Explains Risks of Taking Levaquin

In 1996, the U.S. Food and Drug Administration (FDA) approved the popular antibiotic Levaquin. However, in July 2008, the FDA issued warnings to consumers that Levaquin could increase the risk of developing tendonitis and tendon ruptures for those taking the antibiotic.

The FDA also took action by requiring the drug’s manufacturer, Ortho-McNeil Pharmaceutical, Inc., to put warning labels about these increased risks on the drug’s packaging. Ortho-McNeil Pharmaceutical, which is a subsidiary of Johnson & Johnson, has faced lawsuits from victims who have allegedly sustained injuries from taking the drug.

Ruptured Achilles Tendon is a Risk of Taking Levaquin

Reports indicate that the most serious type if injury associated with taking Levaquin is a rupture in the Achilles tendon. Many victims have been required to endure surgery to repair the damage. Other victims have reportedly suffered tendon ruptures in the hand, bicep, rotator cuff and thumb.

An injury caused by Levaquin can have lasting effects on a victim. If you believe that you have suffered a ruptured tendon or tendonitis from taking Levaquin, you should speak with a Dallas dangerous drug lawyer. You might be able to hold the manufacturer liable for your injury.

If you or someone you know has been injured by taking Levaquin, you should contact an experienced Dallas dangerous drug attorney at the law office of Kay Van Wey at (800) 489-5082.

Be sure to order a free copy of our book, 7 Secrets the Pharmaceutical Industry Does NOT Want You to Know.