Important Safety Information
Hectorol (doxercalciferol capsules and injection) is contraindicated in patients with a tendency toward hypercalcemia or current evidence of vitamin D toxicity. Overdosage of any form of vitamin D is dangerous. View additional Important Safety Information.

Dosing Information

Hectorol® Injection Dosing for Patients on Dialysis

Hectorol® (doxercalciferol injection) dosing must be individualized and based on intact parathyroid hormone (iPTH) levels with monitoring of serum calcium and serum phosphorus levels.1 

Hectorol Injection
Dosage strengths: 4 mcg/2 mL vial, 2mcg/mL vial
Recommended starting dose is 4 mcg three times a week for an iPTH level >400 pg/mL per the Package Insert1
Mean weekly dose at week 12 was 11.0 mcg in a retrospective analysis of 64 hemodialysis patients in a pivotal trial2

The Hectorol 2mcg/mL and the 4mcg/2mL vial options offer simplicity in dosing with consistent concentrations of product in single-use vials that contain no latex.

Our Renal Clinical Consultant Team is a dedicated resource that can assist with Hectorol protocol development and application and/or dosing questions through patient case scenario discussion.

Contact Us

Genzyme Therapeutics
500 Kendall Street
Cambridge, MA 02142

Tel: 617-768-9000
Fax: 617-252-7600
Toll free: 800-745-4447

Contact Genzyme

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Indication

Hectorol (doxercalciferol capsules and injection) is indicated for the treatment of secondary hyperparathyroidism in patients with Stage 3 or Stage 4 chronic kidney disease (capsules) and in patients with chronic kidney disease on dialysis (capsules and injection).

Important Safety Information

  • Hectorol is contraindicated in patients with a tendency towards hypercalcemia or current evidence of vitamin D toxicity.
  • Overdosage of any form of vitamin D is dangerous.
  • Acute hypercalcemia may exacerbate tendencies for cardiac arrhythmias and seizures and may potentiate the action of digitalis drugs.
  • Chronic hypercalcemia can lead to generalized vascular and soft tissue calcification.
  • Pharmacologic doses of vitamin D and its derivatives should be withheld during Hectorol treatment to avoid possible additive effects and hypercalcemia.
  • Magnesium-containing antacids and Hectorol should not be administered concomitantly.
  • Adverse effects of Hectorol treatment are: hypercalcemia, hyperphosphatemia, hypercalciuria, and oversuppression of iPTH.
  • Adverse events reported by ≥ 5% of the Hectorol-treated predialysis patients included: infection, chest pain, constipation, dyspepsia, anemia, dehydration, depression, hypertonia, insomnia, paresthesia, increased cough, dyspnea, and rhinitis.
  • Adverse events reported by ≥ 5% of the Hectorol-treated dialysis patients included: headache, malaise, bradycardia, nausea/vomiting, edema, dizziness, dyspnea, and pruritus.
  • See Hectorol Capsules Full Prescribing Information or Hectorol Injection Full Prescribing Information or call Genzyme Medical Information at 1-800-847-0069.

References

  1. Hectorol (doxercalciferol injection) [package insert]. Cambridge, MA: Genzyme Corp.; Nov 2008.

  2. Maung HM, Elangovan L, Frazao JM, et al. Efficacy and side effects of intermittent intravenous and oral doxercalciferol (1-hydroxyvitamin D2) in dialysis patients with secondary hyperparathyroidism: a sequential comparison. Am J Kidney Dis. 2001;37:532-543.