FDA Alert - Drug Safety Communication: Oral Osteoporosis Drugs (bisphosphonates) - Potential Increased Risk of Esophageal Cancer

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Alert FDA MedWatch Alert
Sent to subscribers of: alendronate systemic, etidronate systemic, ibandronate systemic, risedronate systemic, tiludronate systemic, alendronate, etidronate, ibandronate, risedronate, bisphosphonates
July 21, 2011
Audience: Geriatrics, Family Practice, Internal Medicine.
Includes: Fosamax (alendronate), Actonel (risedronate), Boniva (ibandronate), Atelvia (risedronate delayed release), Didronel (etidronate), and Skelid (tiludronate)
ISSUE: FDA notified healthcare professionals and patients about its ongoing review of data from published studies to evaluate whether use of oral bisphosphonate drugs is associated with an increased risk of cancer of the esophagus. FDA has not concluded that taking an oral bisphosphonate drug increases the risk of esophageal cancer. There are insufficient data to recommend endoscopic screening of asymptomatic patients. FDA will continue to evaluate all available data supporting the safety and effectiveness of bisphosphonate drugs and will update the public when more information becomes available.
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