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These highlights do not include all the information needed to use ATELVIA safely and effectively. See full prescribing information for ATELVIA . ATELVIA ® (risedronate sodium) delayed-release tablets Initial U.S. Approval: 1998
Medication labelWhy this: Advisory · dailymed-prescription
Atelvia is indicated for the treatment of osteoporosis in postmenopausal women. In postmenopausal women, risedronate sodium has been shown to reduce the incidence of vertebral fractures and a composite endpoint of nonvertebral osteoporosis-related fractures [ see Clinical Studies (14.1) ] . The optimal duration of use has not been determined. The safety and effectiveness of Atelvia for the treatment of osteoporosis are based on clinical data of one year 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
- risedronate sodium
- product_names
- risedronate sodium
- ndc
- 0430-0979, 0430-0979-03
- group
- drugs
- license
- us-gov-pd
- attribution
- Courtesy of the National Library of Medicine
- reviewed
- 2026-09-18
- language
- en