| Subject: | FDA Informs Healthcare Providers of Post Marketing Review of Reclast (Zoledronic Acid) |
| Category: | Food and Drug Administration (FDA)
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| Published: | Mon, 29 Jun 2009 - 11:00 am |
| The Food and Drug Administration (FDA) is informing healthcare providers of the results of its postmarketing review of Reclast (Zoledronic Acid), a FDA-approved bisphosphonate administered as a once-yearly intravenous infusion for the treatment of osteoporosis in postmenopausal women and men, Paget's disease of bone, and prevention and treatment of glucocorticoid-induced osteoporosis in patients expected to be on glucocorticoids for at least 12 months. From April 2007 until February 17,... The full article is available to StayAlert subscribers. Click here for a free trial subscription. |
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