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These highlights do not include all the information needed to use ALENDRONATE SODIUM ORAL SOLUTION safely and effectively. See full prescribing information for ALENDRONATE SODIUM ORAL SOLUTION. ALENDRONATE SODIUM oral solution, for oral use Initial U.S. Approval: 1995
Medication labelWhy this: Advisory · dailymed-prescription
Alendronate sodium is indicated for the treatment of osteoporosis in postmenopausal women. In postmenopausal women, alendronate increases bone mass and reduces the incidence of fractures, including those of the hip and spine (vertebral compression fractures) [see Clinical Studies ( 14.1 )]. Alendronate sodium is indicated for treatment to increase bone mass in men with osteoporosis [see Clinical Studies ( 14.3 )]. The optimal duration of use has not been determined. The safety and effectiveness of alendronate for the treatment of osteoporosis are based on clinical data of four years duration. All patients on bisphosphonate therapy should have the need for continued therapy re-evaluated on a periodic basis. Patients at low-risk for fracture should be considered for drug discontinuation after 3 to 5 years of use. Patients who discontinue therapy should have their risk for fracture re-evaluated periodically.
- generic_name
- alendronate sodium
- product_names
- Alendronate Sodium
- ndc
- 0054-0282, 0054-0282-59
- group
- drugs
- license
- us-gov-pd
- attribution
- Courtesy of the National Library of Medicine
- reviewed
- 2026-09-18
- language
- en