Unlabeled Use:
Contraindicated in:
Use Cautiously in:
Seen primarily as manifestations of toxicity (hypercalcemia)
CV: arrhythmias, hypertension.
Derm: pruritus.
EENT: conjunctivitis, photophobia, rhinorrhea.
F and E: hypercalcemia.
GI: abdominal pain, anorexia, constipation, dry mouth, ↑ liver enzymes, metallic taste, nausea, PANCREATITIS, polydipsia, vomiting.
GU: albuminuria, azotemia, ↓ libido, nocturia, polyuria.
Local: pain at injection site.
Metab: hyperthermia, weight loss.
MS: bone pain, metastatic calcification, muscle pain.
Neuro: headache, somnolence, weakness.
Misc: hypersensitivity reactions.
Drug-Drug:
Drug-Food:
Hypocalcemia During Dialysis
Hypoparathyroidism
6 yr): 0.25 mcg/day initially; if needed, may ↑ dose by 0.25 mcg/day at 24 wk intervals (typical dosage = 0.52 mcg/day).
5 yr): <1 yr 0.040.08 mcg/kg/day15 yr 0.250.75 mcg/day.Predialysis Patients
3 yr): 0.25 mcg/day; if needed, may ↑ dosage up to 0.5 mcg/day.Rickets
Hypocalcemia in Premature Infants
Calcijex, Rocaltrol
Absorption: Well absorbed following oral administration.
Distribution: Crosses the placenta and enters breast milk.
Protein Binding: 99.9%.
Metabolism/Excretion: Undergoes enterohepatic recycling and is excreted mostly in bile.
Half-life: 58 hr (with normal renal function); 1622 hr (chronic renal failure).
NDC Code*