Mistrial Declared in FOSAMAX® (alendronate sodium) New Jersey State Court Trial
March 18, 2013 12:49 pm ET
WHITEHOUSE STATION, N.J., March 18, 2013 – Merck, known outside the United States and Canada as MSD, today said a mistrial was declared by Judge Carol E. Higbee of the Superior Court for Atlantic County, N.J., in the Su v. Merck case.
One week after opening statements were given, the plaintiff suffered a serious health complication unrelated to her use of FOSAMAX. As a result of her inability to proceed with the trial, Judge Higbee declared a mistrial.
The plaintiff alleged that she used FOSAMAX and that she sustained a femur fracture. No decision has been made as to when the case may be re-tried.
Merck is represented in the case by Christy Jones of Butler, Snow, O’Mara, Stevens & Cannada, PLLC, Ridgeland, Miss.; Tarek Ismail of Goldman Ismail Tomaselli Brennan & Baum, LLP, Chicago, Ill.; and Eileen Oakes Muskett of Fox Rothschild LLP, Atlantic City, N.J.
Status of Litigation
This is the eighth FOSAMAX case to go to trial and the first case to be tried where the plaintiff alleges she sustained a femur fracture in association with the use of FOSAMAX. All of the earlier trials – five federal and two New Jersey state cases – involved allegations associated with jaw-related problems. Merck won five of those seven prior trials. Among the two losses, the company is appealing the jury verdict in Boles v. Merck and has filed a post-trial motion for judgment as a matter of law in Scheinberg v. Merck.
As of Dec. 31, 2012, approximately 4,560 cases, which include approximately 5,140 plaintiff groups, had been filed and were pending against Merck in either federal or state court. In approximately 1,230 of these cases, plaintiffs allege that they sustained a jaw-related injury, while the plaintiffs in the approximately 3,330 other cases allege that they sustained a femur fracture and/or other bone-related injuries.
The next trial involving claims of a femur fracture in association with the use of FOSAMAX, Glynn v. Merck, is scheduled to begin April 8, 2013, in the U.S. District Court for the District of New Jersey.
About FOSAMAX (alendronate sodium)
FOSAMAX is indicated for the treatment and prevention of osteoporosis in postmenopausal women. The safety and effectiveness of FOSAMAX for the treatment of osteoporosis are based on clinical data of 4 years’ duration. FOSAMAX should not be used in patients who have certain disorders of the esophagus that delay emptying, who are unable to stand or sit upright for at least 30 minutes, who have low levels of calcium in their blood, or in patients who are allergic to FOSAMAX. Some patients may develop severe digestive reactions including irritation, inflammation, or ulceration of the esophagus. Dosing instructions should be followed and patients who experience new or worsening heartburn, difficulty or pain when swallowing, or chest pain should stop taking the drug and call their doctor right away. Patients who develop severe bone, joint, and/or muscle pain at any time should contact their doctor. Osteonecrosis of the jaw, generally associated with tooth extraction and/or local infection, with delayed healing, has been reported in patients taking bisphosphonates, including FOSAMAX. Atypical femur fractures have been reported in patients taking bisphosphonates.
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The Prescribing information and Medication Guide for FOSAMAX® (alendronate sodium) are attached and are available at:
FOSAMAX® is a registered trademark of Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Whitehouse Station, N.J., U.S.A.