Consumer Alert Fosamax Femur Fracture Update
August 17, 2012
In addition to litigation alleging osteonecrosis of the jaw ("ONJ") and musculoskeletal pain arising from FOSAMAX® use 1, recent studies, reports, and news stories have indicated that long term use of the drug may be linked to atypical femur fractures.2 These fractures can occur during low impact activities and may be preceded by thigh pain for weeks or months prior to the fracture.3 FOSAMAX® is manufactured by Merck, and is prescribed for the treatment and prevention of osteoporosis, and the treatment of Paget’s disease
In March 2010, the FDA issued a Drug Safety Communication about bisphosphonates, a class of drugs that includes FOSAMAX®, in which it recommended that health care providers “[b]e aware of the possible risk of atypical subtrochanteric femur fractures in patients taking oral bisphosphonates.4” Seven months later, the FDA issued a safety update, announcing that the “risk of atypical fractures of the thigh, known as subtrochanteric and diaphyseal femur fractures, in patients who take bisphosphonates for osteoporosis” would “be added to the Warnings and Precautions section of the labels of all bisphosphonate drugs approved for the prevention or treatment of osteoporosis.5”
Litigation claiming FOSAMAX® caused atypical femur fractures has started across the nation, and on May 23, 2011, these cases were consolidated into a Multi-District Litigation (MDL). This means that all cases in federal court alleging that FOSAMAX®, or FOSAMAX® and an additional bisphosphonate, caused an atypical femur fracture are now consolidated and centralized in the U.S. District Court for the District of New Jersey6. Currently there are over 500 cases pending in the MDL.
Robins, Kaplan, Miller & Ciresi L.L.P. is actively involved in litigating these cases. Please feel free to contact our offices at 1-800-553-9910.
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