FDA
Risedronate Sodium
The FDA lists this product in 31 strengths and forms.
Indications
Risedronate sodium delayed-release tablets are bisphosphonate in a delayed-release formulation and is indicated for treatment of postmenopausal osteoporosis (1.1) Limitations of Use Optimal duration of use has not been determined. For patients at low-risk for fracture, consider drug discontinuation after 3 to 5 years of use (1.2).
1.1Postmenopausal Osteoporosis
Risedronate sodium delayed-release tablets are 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) ].
1.2Important Limitations of Use
The optimal duration of use has not been determined. The safety and effectiveness of risedronate sodium delayed-release tablets 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.
Contraindications
Risedronate sodium delayed-release tablets contraindicated in patients with the following conditions: 1. Abnormalities of the esophagus which delay esophageal emptying such as stricture or achalasia [ see Warnings and Precautions (5.2) ] 2. Inability to stand or sit upright for at least 30 minutes [ see Dosage and Administration (2), Warnings and Precautions (5.2) ] 3. Hypocalcemia [ see Warnings and Precautions (5.3) ] 4.
Known hypersensitivity to any component of this product. Angioedema, generalized rash, bullous skin reactions, Stevens-Johnson syndrome and toxic epidermal necrolysis, have been reported [ see Adverse Reactions (6.2) ]
- Abnormalities of the esophagus which delay esophageal emptying such as stricture or achalasia (4, 5.2)
- Inability to stand or sit upright for at least 30 minutes (4, 5.2)
- Hypocalcemia (4, 5.3)
- Known hypersensitivity to any component of this product (4, 6.2)
Warnings and precautions
At a glance
- Brand name
- Risedronate Sodium
- Route
- Oral
- Dosage form
- Tablet, delayed release
- Applicant
- Sun Pharm
- Status
- Discontinued
- FDA approval
- 9 Jul 2019
- Application
- ANDA203925-001



