- Management of hypocalcemia in patients undergoing chronic renal hemodialysis
- Treatment of hypocalcemic tetany in premature infants.
- Available as 1 mcg/mL injection
- Store at room temperature
- Protect from light and excessive heat in original container
- Solutions Compatible: D5W, NS, Sterile Water for Injection
- Additives/Above Cassette Compatible: no information
- Y-site Compatible: no information
- Incompatible: do not mix with any other drug
(For approved routes of administration by nursing personnel, refer to Policy for the Administration of Intravenous Medications.)
SC | NO |
IM | NO |
IV Direct |
YES |
IV Intermittent Infusion | YES Usual dilution: 1 mcg/mL Infusion time: 15 minutes |
IV Continuous Infusion | NO |
(For neonatal dosages, refer to Neonatal IV Drug Manual.)
Pediatrics:
- Hemodialysis patients: 0.01-0.05 mcg/kg/dose three times weekly
Adults:
- Hemodialysis patients: 0.5 mcg (0.1 mcg/kg) IV 3 times/week; may increase dosage by 0.25 - 0.5 mcg increments at 2-4 week intervals until optimal response is achieved. [Range 0.5-3 mcg].
- Mild pain at site of injection
- Hypercalcemia
- Vitamin D intoxication
- Excessive dosage induces hypercalcemia which can lead to generalized vascular calcification, nephrocalcinosis, calcifications of cornea or other soft tissues
- Early and late signs of vitamin D intoxication and hypercalcemia:
- Early: weakness, headache, somnolence, nausea, vomiting, thirst,
dry mouth, constipation, muscle and bone pain, metallic taste,
cardiac arrhythmias- Late: polyuria, polydipsia, anorexia, conjunctivitis, nocturia, pancreatitis,
photophobia, rhinorrhea, pruritus, hyperthermia, decreased libido,
ectopic calcification, cardiac arrhythmias and hypertension - Treatment of hypercalcemia includes discontinuation of calcitriol, institution of a low calcium diet and withdrawal of calcium supplementation
- Do not use in combination with magnesium containing antacids, as hypermagnesemia may develop
- Monitor serum calcium and phosphorus levels