Absorption: IV administration results in complete bioavailability.
Distribution: Rapidly absorbed by bone. Reaches high concentrations in bone, liver, spleen, teeth, and tracheal cartilage. Approximately 50% of a dose is retained by bone and then slowly released.
Metabolism/Excretion: 50% is excreted unchanged in the urine.
Half-life: Elimination half-life from plasma is biphasic 1st phase 1.6 hr, 2nd phase 27.2 hr. Elimination half-life from bone is 300 days.
Contraindicated in:
Use Cautiously in:
EENT: conjunctivitis, blurred vision, eye pain/inflammation, rhinitis.
Neuro: fatigue.
Resp: rales.
CV: arrhythmias, hypertension, syncope, tachycardia.
GI: nausea, abdominal pain, anorexia, constipation, vomiting.
F and E: hypocalcemia, hypokalemia, hypomagnesemia, hypophosphatemia, fluid overload.
GU: nephrotoxicity.
Hemat: leukopenia, anemia.
Local: phlebitis at injection site.
Metab: hypothyroidism.
MS: muscle stiffness, musculoskeletal pain, femur fractures, osteonecrosis (primarily of jaw).
Misc: fever, generalized pain.
Drug-Drug:
Hypercalcemia of Malignancy
Osteolytic Lesions from Multiple Myeloma
Osteolytic Lesions from Metastatic Breast Cancer
Pagets Disease
Therapeutic Classification: bone resorption inhibitors
Pharmacologic Classification: biphosphonates, hypocalcemics
NDC Code*