risedronate sodium
risedronate sodium
Pharmacologic class: Bisphosphonate
Therapeutic class: Calcium regulator
Pregnancy risk category C
Action
Inhibits osteoclast-mediated bone resorption. Also exerts antiresorptive effect, probably by directly inhibiting mature osteoclast activity or indirectly inhibiting osteoblasts.
Availability
Tablets: 5 mg, 30 mg, 35 mg, 150 mg
Tablets (delayed-release): 35 mg
Indications and dosages
➣ Prevention of postmenopausal osteoporosis
Adults: 5 mg P.O. daily or 35 mg P.O. weekly (immediate-release)
➣ Treatment of postmenopausal osteoporosis
Adults: 5 mg P.O. daily, or 35 mg P.O. weekly, or 150 mg P.O. monthly (immediate-release). Or, 35 mg P.O. weekly (delayed-release).
➣ Osteoporosis in men
Adults: 35 mg (immediate-release) P.O. weekly
➣ Glucocorticoid-induced osteoporosis
Adults: 5 mg (immediate-release) P.O. daily
➣ Paget's disease
Adults: 30 mg (immediate-release) P.O. daily for 2 months. If indicated, may retreat with same dosage after post-treatment observation period of at least 2 months.
Off-label uses
• Hypercalcemia of malignancy
• Primary hyperparathyroidism
Contraindications
• Hypersensitivity to drug, its components, or other bisphosphonates
• Hypocalcemia
• Inability to stand or sit upright for at least 30 minutes
• Esophageal abnormalities that delay esophageal emptying, such as stricture or achalasia
Precautions
Use cautiously in:
• hypotension, upper GI disorders, difficulty swallowing
• severe renal impairment with creatinine clearance less than 30 ml/minute (not recommended)
• pregnant or breastfeeding patients
• children (use not indicated)
Administration
• Be aware that hypocalcemia and other disturbances of bone and mineral metabolism should be effectively treated before starting drug.
• Give immediate-release tablets with 6 to 8 oz of water 30 minutes before first food or beverage of day (other than water).
• Give delayed-release tablets in the morning immediately after breakfast with at least 4 oz of plain water.
See Make sure patient stays upright for at least 30 minutes after taking.
• Be aware that patient with poor dietary intake may need calcium and vitamin D supplements.
• Give calcium, magnesium, or aluminum supplements or antacids at different time of day so they don't interfere with risedronate absorption.
Adverse reactions
CNS: headache, anxiety, depression, dizziness, vertigo, syncope, asthenia
CV: hypertension, vasodilation, angina, chest pain, cardiovascular disorder, peripheral edema
EENT: cataract, conjunctivitis, dry eyes, otitis media, rhinitis, sinusitis, pharyngitis
GI: nausea, vomiting, diarrhea, constipation, abdominal pain, dyspepsia, flatulence, gastroenteritis, colitis, esophageal irritation, dry mouth, anorexia, esophageal stricture or perforation (rare)
GU: urinary tract infection
Hematologic: anemia
Musculoskeletal: bone, back, or joint pain; bone fracture; bursitis; myalgia; arthritis; leg and muscle cramps; jaw osteonecrosis
Respiratory: crackles, cough, bronchitis, pneumonia
Skin: rash, pruritus, ecchymosis, skin cancer
Other: accidental injury, infection, neck pain, flulike symptoms, allergic reactions, neoplasm, hypersensitivity reactions including angioedema (rare)
Interactions
Drug-drug. Antacids, aspirin, calcium-or magnesium-based supplements or laxatives, iron preparations: decreased risedronate absorption
Nonsteroidal anti-inflammatory drugs, salicylates: increased GI irritation
Drug-diagnostic tests. Bone-imaging diagnostic agents: interference with test agents
Calcium, phosphorus: decreased levels
Drug-food. Any food: decreased drug absorption
Patient monitoring
• Watch for difficulty swallowing and signs and symptoms of esophageal irritation. Discontinue drug if new or worsening symptoms occur.
• Assess skin for unusual findings that may indicate skin cancer.
• Monitor patient for severe bone, joint, or muscle pain; consider discontinuing drug if symptoms are severe
Patient teaching
• Advise patient to read patient information insert before starting therapy.
See Stress importance of taking immediate-release tablets with a full glass (6 to 8 oz) of water at least 30 minutes before first food or drink of day and delayed-release tablets in the morning immediately after breakfast with at least 4 oz of plain water. Tell patient to stay upright for at least 30 minutes afterward.
See Instruct patient to stop drug and notify prescriber if difficulty or pain on swallowing, midline chest pain, or severe, persistent heartburn occurs.
• Tell patient that chewing or sucking tablet may cause mouth irritation.
• Tell patient to report signs and symptoms of colitis.
• Advise patient taking calcium-, magnesium-, or aluminum-based supplements or antacids to take them at least 2 hours after risedronate.
• Advise patient to promptly report leg cramps or bone, joint, or jaw pain.
• As appropriate, review all other significant and life-threatening adverse reactions and interactions, especially those related to the drugs, tests, and foods mentioned above.