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In the News
Prolia® (denosumab) in the News
Sep. 20, 2012
Press Release: FDA Approves New Indication For Prolia® (Denosumab) For The Treatment Of Bone Loss In Men With Osteoporosis At High Risk For Fracture
Sep. 20, 2012
Amgen Modifies U.S. Prescribing Information for Prolia® (denosumab)
Sep. 20, 2012
Amgen Modifies Prolia® Risk Evaluation and Mitigation Strategy (REMS) Materials (US)
Jun. 7, 2012
Amgen Modifies Prolia® Risk Evaluation and Mitigation Strategy (REMS) Materials (US)
May 11, 2012
Amgen Modifies U.S. Prescribing Information for Prolia® (denosumab)
Sep. 19, 2011
Press Release: FDA Approves New Indications for Prolia® (denosumab) for the Treatment of Bone Loss in Patients with Prostate or Breast Cancer Undergoing Hormone Ablation Therapy
Sep. 19, 2011
Amgen Modifies U.S. Prescribing Information for Prolia® (denosumab)
Sep. 19, 2011
Amgen Modifies Prolia® Risk Evaluation and Mitigation Strategy (REMS) Materials (US)
Jul. 22, 2011
Amgen Modifies U.S. Prescribing Information for Prolia® (denosumab)
Aug. 6, 2010
Prolia™ (denosumab) Receives Approval in Switzerland and Canada
Jun. 8, 2010
Amgen Issues Statement About Prolia® (denosumab) Approval in Australia
Jun. 1, 2010
Press Release: FDA Approves Amgen's Prolia™ (denosumab) for Treatment of Postmenopausal Women with Osteoporosis at High Risk for Fracture
Jun. 1, 2010
Prolia™ Prescribing Information (US)
Jun. 1, 2010
Prolia™ Risk Evaluation and Mitigation Strategy (REMS) Materials (US)
May 28, 2010
Press Release: Prolia® (denosumab) Granted Marketing Authorization in the European Union
May 28, 2010
Prolia® (denosumab) Summary of Medicinal Product Characteristics (EU)

Background Documents

Prescribing information for Prolia™

 


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