Osteoporosis Drugs Require Better Labeling: FDA

By IBTimes Staff Reporter: Subscribe to IBTimes's

September 10, 2011 9:26 AM EDT

Warner Chilcott Plc (WCRX), Roche Holding AG (ROG), Merck & Co. and Novartis AG (NOVN) need to change the labeling of Bisphosphonates, a medicine taken by osteoporosis patients, the Food and Drug Administration has said.  

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The label should come with a clarification on the duration of taking the medicine. However, the FDA advisory committee could not agree on the time limit to be given on the labeling, citing absence of sufficient data to identify the ideal time limit of the medication.

The FDA has been evaluating the safety of the medicine for last four years and found possible co-relation between long-term use of the medicine and atypical thigh bone fracture and jawbone deterioration in 2010.

Post-menopausal women who suffer from osteoporosis are often found to be taking these medicines and a study showed a possible connection between the long-term medication and increasing rate of esophageal cancer risks. A study done in 2009 used the data from FDA's Adverse Event Reporting System and established a relation between the medicine and esophageal cancer. The research was published in the New England Journal of Medicine.

An estimation of 9 percent of osteoporosis patients taking this medicine for more than three years and almost one percent taking them for more than five years without knowing the consequences of the drugs is troubling, the FDA believes.

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According to the panel, the revised label of the Bisphosphonates should "be very clear that efficacy may fall off after a period of time, perhaps five years."

 After the 17-6 vote on labeling clarification that took place in Adelphi, Maryland, panelist Lewis Nelson, director of the medical toxicology fellowship program at New York University, said: "Serious concerns have been raised about the risks, and those need to be continually evaluated as well."  

In its own study done on the women who had been taking the medicine for over five years, the FDA concluded that no firm result on benefit or harm or evidence of "clear and consistent" reduced fracture risk had been found, Theresa Kehoe, MD and FDA scientist, told the panel.

Bisphosphonates medicines include Aclasta, Actonel, Altevia, Boniva, Fosamax, and Relecast.

In 2010, sales of these medicines reached $7.6 billion worldwide.

This article is copyrighted by International Business Times, the business news leader
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