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| (eh-TIH-DROE-nate die-SO-dee-uhm) |
| Didronel |
| Tablets: 200 mg |
| Tablets: 400 mg |
| Didronel IV |
| Injection: 30 mg/mL |
| Class: Hormone, Biphosphonates |
Action Inhibits normal and abnormal bone resorption; reduces bone formation.
Indications Treatment of symptomatic Paget disease; prevention and treatment of heterotopic ossification; treatment of hypercalcemia of malignancy.
Treatment of postmenopausal osteoporosis.
Contraindications Hypersensitivity to biphosphonates; patients with class Dc and higher renal functional impairment (serum creatinine greater than 5 mg/dL).
Paget Disease
Adults: Initial treatment: PO 5 to 10 mg/kg/day (not to exceed 6 mo) or 11 to 20 mg/kg/day (not to exceed 3 mo). Reserve doses greater than 10 mg/kg/day for specific situations. Retreatment: Initiate only after etidronate-free period of at least 90 days and if there is evidence of active disease.
Heterotopic Ossification from Spinal Cord Injury
Adults: PO 20 mg/kg/day for 2 wk followed by 10 mg/kg/day for 10 wk; total treatment period is 12 wk.
Heterotopic Ossification Complicating Total Hip Replacement
Adults: PO 20 mg/kg/day for 1 mo preoperatively followed by 20 mg/kg/day for 3 mo postoperatively.
Hypercalcemia
Adults: IV 7.5 mg/kg/day for 3 successive days given by slow infusion (over a period of at least 2 hr). Retreatment may be needed; wait at least 7 days between courses. Adjust dose for renal impairment. Regimen of oral etidronate (20 mg/kg/day for 30 days) may be started after last infusion.
Interactions None well documented.
Calcium supplements, antacids, foods: Products containing calcium and other multi-valent cations interfere with etidronate absorption.
EENT: Metallic or altered taste; loss of taste. GI: Diarrhea; nausea; constipation; stomatitis; diarrhea in enterocolitis patients. GU: Abnormal elevations of serum creatinine and BUN; mild to moderate abnormalities in renal function. OTHER: Hypersensitivity (eg, angioedema, urticaria, rash, pruritus); increased or recurrent bone pain in Paget disease; hypocalcemia; fractures with excessive doses; convulsions; hypophosphatemia; hypomagnesemia.
Pregnancy: Category C. Lactation: Undetermined. Children: Safety and efficacy not established. Paget disease: Response may be slow and may continue for months after treatment has been discontinued. Dosage must not be prematurely increased or treatment prematurely reinitiated until patient has had at least 90-day etidronate-free interval. GI disorders: Use this drug with caution in patients with active upper GI problems such as dysphagia (difficulty swallowing); symptomatic esophageal diseases; gastritis; duodenitis or ulcers.
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