section name header

Pronunciation

pa-MID-roe-nate audio

Indications

REMS

Action

Therapeutic Effects:

Pharmacokinetics

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.

Contraind./Precautions

Contraindicated in:

Use Cautiously in:

Adv. Reactions/Side Effects

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.

Interactions

Drug-Drug:

Route/Dosage

Single doses should not exceed 90 mg

Hypercalcemia of Malignancy

Osteolytic Lesions from Multiple Myeloma

Osteolytic Lesions from Metastatic Breast Cancer

Paget’s Disease

Implementation

US Brand Names

Aredia

Classifications

Therapeutic Classification: bone resorption inhibitors

Pharmacologic Classification: biphosphonates, hypocalcemics

Availability

(Generic available)

Time/Action Profile

(effect on serum calcium)

ROUTEONSETPEAKDURATION
IV24 hr7 daysunknown

Assessment

Lab Test Considerations:

Pot. Nursing Diagnoses

Patient/Family Teaching

Evaluation/Desired Outcomes

Code

NDC Code*