Victims continue to sue Merck for Fosamax® femur fractures

Consumer Drug Report recently reported a case filed by another victim of Fosamax femur fracture injuries. According to the drug risk information resource, a woman by the name of Reba Inez Patton and her husband Patrick Patton filed a claim alleging that bisphosphonate medication, Fosamax and Boniva®, caused her to suffer from a low-energy femur fracture in December 2010. The fracture is a rare form of bone injury which may occur with little or no trauma to the victim.

The Fosamax lawsuit was filed on December 15, 2011 against drug maker Merck & Co., maker of Fosamax, and GlaxoSmithKline (GSK), maker of Boniva, in the Superior Court of New Jersey.

The complaint filed by the Patton’s alleges that both Merck and GSK falsely marketed the medications, which are designed to strengthen bones in women diagnosed with osteoporosis, claiming that the companies failed to provide sufficient warnings of the femur fracture risks.

Due to the femur fracture injuries, Mrs. Patton suffers severe and permanent damage requiring ongoing medical care.

Thousands of Fosamax femur fracture lawsuits have been filed against Merck & Co. all of which make similar allegations that the drug company failed to properly warn of the risks associated with long term use of Fosamax.

Fosamax was designed to treat osteoporosis, a chronic condition in which bones become brittle and break. The Food and Drug Administration approved Fosamax in October of 1995. Since its approval, over 20 million patients have taken the medication. The drug grew in popularity and prior to the release of a generic, Fosamax brought in revenues of $3 million.

All lawsuits filed against Merck have been consolidated as part of a multidistrict litigation and is centralized in the U.S. District court for the District of New Jersey.