Zoledronic Acid-Mannitol-Water (zoledronic acid in mannitol and water for injection)

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Last reviewed · Source: First Databank (FDB) drug data

Overview

Zoledronic acid, a synthetic imidazole bisphosphonate analog of pyrophosphate, is a bone resorption inhibitor.

Zoledronic acid, a synthetic imidazole bisphosphonate analog of pyrophosphate, is an inhibitor of osteoclast-mediated bone resorption. Zoledronic acid is structurally and pharmacologically related to alendronate, risedronate, and pamidronate.

Zoledronic acid inhibits increased osteoclastic activity and skeletal calcium release induced by tumors. In patients with hypercalcemia of malignancy, zoledronic acid decreases serum calcium and phosphorus and increases urinary calcium and phosphorus excretion.

Zoledronic acid is eliminated in urine as unchanged drug. In patients with cancer and bone metastases, an average of 39% of an IV dose of zoledronic acid was excreted in urine within 24 hours. Nonrenal clearance is believed to result from uptake of the drug by bone; subsequently, the drug is released systemically via bone turnover.

Results of in vitro studies indicate that zoledronic acid does not inhibit the cytochrome P-450 (CYP) enzyme system.

USES: This medication is used to treat a certain type of bone disease (Paget's disease) that causes abnormal and weak bones. Zoledronic acid is also used to treat bone loss (osteoporosis) in men and in women after menopause who are at high risk of having broken bones (fractures). It may also be used to treat or prevent osteoporosis in people who are taking corticosteroid medications (such as prednisone) for long periods.

It works by slowing the breakdown of bone and keeping bones strong. It also helps to reduce the risk of broken bones (fractures). This medication belongs to a class of drugs known as bisphosphonates.

Generic name: zoledronic acid in mannitol and water for injection
Pronunciation: (ZOLE-eh-dron-ick)

Reference product & biosimilars

No reference, biosimilar or interchangeable associated with this drug.

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Indications

The following indications are listed for Zoledronic Acid-Mannitol-Water:

  • Glucocorticoid-Induced Osteoporosis
  • Osteoporosis In Male Patient
  • Osteoporosis In Postmenopausal Woman At High Risk For Fracture
  • Paget's Disease Of Bone
  • Post-Menopausal Osteoporosis Prevention
  • Prevention Of Glucocorticoid-Induced Osteoporosis

Also known as: Glucocorticoid Hormone-Induced Osteoporosis, Glucocorticoid Induced Osteoporosis, Glucocorticoid-Induced Osteoporosis Prophylaxis, Glycocorticoid-Induced Osteoporosis, Osteitis Deformans, Osteoporosis In Men, Postmenopausal Osteoporosis In Woman With High Fracture Risk, Postmenopausal Osteoporosis Prophylaxis, Postmenopausal Osteoporosis With High Fracture Risk.

Dosing

Dosage of zoledronic acid, which is commercially available for parenteral use as the monohydrate, is calculated on the anhydrous basis.

Drug interactions

There is no enhanced messaging for this drug.

Contraindications

Known hypersensitivity to zoledronic acid, other bisphosphonates, or any ingredient in the formulations.

Hypocalcemia.

Use of zoledronic acid for prevention or treatment of osteoporosis or for treatment of Paget disease of bone is contraindicated in patients with creatinine clearance of less than 35 mL/minute or those with evidence of acute renal impairment.

Adverse reactions

There is no enhanced messaging for this drug.

Precautions

No enhanced messaging available.

ICD codes

No ICD codes are available for this drug.

Formulary status

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Last reviewed · Source: First Databank (FDB) drug data