Details About Generic Salt ::  Etidrona

Main Medicine Class:: Hormone, Biphosphonates   

(eh-TIH-DROE-nate die-SO-dee-uhm)

Didronel

Tablets: 200 mg

Tablets: 400 mg

Didronel IV

Injection: 30 mg/mL

Class: Hormone, Biphosphonates

Drugs Class ::

 Action Inhibits normal and abnormal bone resorption; reduces bone formation.

Indications for Drugs ::

 Indications Treatment of symptomatic t disease; prevention and treatment of heterotopic ossification; treatment of hypercalcemia of malignancy.

Treatment of postmenopausal osteoporosis.

Drug Dose ::

 Route/Dosage

t 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.

Contraindication ::

 Contraindications Hypersensitivity to biphosphonates; patients with class Dc and higher renal functional impairment (serum creatinine greater than 5 mg/dL).

Drug Precautions ::

 Precautions

Pregnancy: Category C. Lactation: Undetermined. Children: Safety and efficacy not established. t 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.

Drug Side Effects ::

 Adverse Reactions

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 t disease; hypocalcemia; fractures with excessive doses; convulsions; hypophosphatemia; hypomagnesemia.

Drug Mode of Action ::  

 Action Inhibits normal and abnormal bone resorption; reduces bone formation.

Drug Interactions ::

 Interactions None well documented.

Drug Assesment ::

 Assessment/Interventions

• Obtain patient history, including drug history and any known allergies. Note any hypersensitivity to biphosphonates.
• Record dates of any previous treatments with etidronate.
• Treatment of hypocalcemia includes IV calcium administration.
• Monitor serum calcium, phosphate, potassium, BUN, and creatinine.
• Monitor renal status throughout treatment.

Drug Storage/Management ::

 Administration/Storage

• Have patient take drug on empty stomach 2 hr before meals.
• Administer oral medication as a single dose. If GI upset occurs, dose may be divided.
• To maximize absorption of drug, have patient avoid food high in calcium (eg, milk and milk products), vitamins with mineral supplements and antacids high in metals within 2 hr of dosing.
• Dilute daily IV dose in at least 250 mL of sterile normal saline.
• Slow IV infusion is important. Infuse diluted dose over 2 hr or more.
• Store diluted dose at room temperature no longer than 48 hr.
• Store IV medication away from excessive heat.

Drug Notes ::

 Patient/Family Education

• Instruct patient to avoid eating 2 hr before and 2 hr after taking medication because absorption of drug is reduced by food.
• Advise patient to avoid vitamins, mineral supplements, and antacids that are high in metals, especially calcium, iron, magnesium, and aluminum.
• Instruct patient to maintain adequate intake of foods containing calcium and vitamin D within 2 hr of taking etidronate.
• Inform patient of transient effect of metallic or altered taste or loss of taste.
• Tell patient to report the following symptoms to health care provider: rash, respiratory difficulty, GI upset, visual disturbances, jaundice.
• Instruct patient not to take any OTC medications without consulting the health care provider.

Disclaimer ::

The Information available on this site is for only Informational Purpose , before any use of this information please consult your Doctor .Price of the drugs indicated above may not match to real price due to many possible reasons may , including local taxes etc.. These are only approximate indicative prices of the drug.