The Alliance for Better Bone Health, a collaboration between Procter & Gamble Pharmaceuticals and Sanofi-Aventis US, has announced that FDA has approved a new once-a-month dose of Actonel tablets for the treatment and prevention of postmenopausal osteoporosis.
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Actonel is approved to reduce the risk of fractures in postmenopausal women with osteoporosis.
The FDA approval of the once-a-month dose is based on a study comparing Actonel 150mg once monthly to Actonel 5mg daily. Similar increases in bone mineral density (BMD) were seen among patients under once-a-month or daily dosing regimens.
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