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Product Highlights

Product Highlights

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Educational Resources

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Journal Reprints
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Holick Vitamin D Reprint
Holick MF et al: Prevalence Of Vitamin D Inadequacy among Postmenopausal North American Women Receiving Osteoporosis Therapy J Clin Endocrinol Metal. 2005;90(6):3215-3224.
One unit per package
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BMD Patient Primer BMD Patient Primer
1 unit (each unit contains 10 brochures)
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Ask Me T-score Tear Sheet
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Lenticular Poster Lenticular Poster
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Prescribing Information

FOSAMAX® (alendronate sodium)
Prescribing Information Prescribing Information [PDF]
Patient Product Information Patient Product Information (Once Daily)
Patient Product Information Patient Product Information (Once Weekly)

FOSAMAX PLUS D (alendronate sodium/cholecalciferol)
Prescribing Information Prescribing Information [PDF]
Patient Product Information Patient Product Information [PDF]

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Important Product Information

IMPORTANT PRODUCT INFORMATION:

FOSAMAX and FOSAMAX PLUS D are indicated for the treatment of osteoporosis in postmenopausal women. For the treatment of osteoporosis, FOSAMAX and FOSAMAX PLUS D increase bone mass and reduce the incidence of fractures, including those of the hip and spine (vertebral compression fractures).

FOSAMAX and FOSAMAX PLUS D are contraindicated in patients with esophageal abnormalities which delay esophageal emptying (eg, stricture or achalasia) and in patients unable to stand or sit upright for at least 30 minutes. Patients at increased risk of aspiration should not receive FOSAMAX oral solution. FOSAMAX and FOSAMAX PLUS D are contraindicated in patients with hypocalcemia (see WARNINGS AND PRECAUTIONS) and in patients with hypersensitivity to any component of these products. Hypersensitivity reactions including urticaria and angioedema have been reported. FOSAMAX and FOSAMAX PLUS D, like other bisphosphonates, may cause local irritation of the upper gastrointestinal mucosa.

In postmarketing experience, severe and occasionally incapacitating bone, joint, and/or muscle pain has been reported in patients taking bisphosphonates that are approved for the prevention and treatment of osteoporosis. The time to onset of symptoms varied from one day to several months after starting the drug. Discontinue use if severe symptoms develop. Most patients had relief of symptoms after stopping treatment.

Before prescribing FOSAMAX or FOSAMAX PLUS D, please see the Prescribing Information and Patient Product Information.

COZAAR and HYZAAR are registered trademarks of E.I. du Pont de Nemours and Company, Wilmington, Delaware, USA
FOSAMAX PLUS D is a trademark of Merck & Co., Inc.
VYTORIN and ZETIA are registered trademarks of MSP Singapore Company, LLC. View the Merck/Schering-Plough privacy policy.
All other brand names are registered trademarks of Merck & Co., Inc.
MerckServices and MerckSource are registered trademarks of Merck & Co., Inc.
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