Prolia approved for postmenopausal osteoporosis - ONA

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Prolia approved for postmenopausal osteoporosis - ONA

oncologynurseadvisor.com

The FDA has approved Prolia (denosumab, from Amgen) for the treatment of postmenopausal women with osteoporosis at high risk for fracture, defined as a history of osteoporotic fracture, or multiple risk factors for fracture; or patients who have failed or are intolerant to other available osteoporosis therapy.

View full resource at oncologynurseadvisor.com

Tags: Fracture, Osteoporosis, Osteoporosis Medication, Women's Health, FDA, Prolia, Amgen

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Prolia approved for postmenopausal osteoporosis http://goo.gl/fb/bGLvd

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medicalnewstoday.com — “Postmenopausal females with osteoporosis or low bone mass who are on Prolia (denosumab) treatment were found to have continued increase in BMD (bone mineral density) for up to eight years, Amgen aView full resource at medicalnewstoday.com

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qualitypointtech.net — “Amgen (NASDAQ: AMGN) announced that it will present data from several Prolia® (denosumab) studies, including eight year efficacy and safety data from a Phase 2 extension study in women with postmenopausal osteoporosis with low bone mineral density (BMD), at the 2011 American Society for Bone and Mineral Research (ASBMR) Annual Meeting in San Diego, Calif. from Sept. 16-20, 2011.View full resource at qualitypointtech.net

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dailymail.co.uk — “Post-menopausal women at increased risk of fractures should be treated with Prolia if other treatments are unsuitable, says the drug rationing body Nice.View full resource at dailymail.co.uk

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