section name header

Pronunciation

DOX-er-kal-SIF-e-role

Classifications

Therapeutic Classification: vitamins

Pharmacologic Classification: fat soluble vitamins

Indications

REMS


Action

  • Requires activation in the liver to create the active form of vitamin D2.
  • Promotes the absorption of calcium and decreases parathyroid hormone concentrations.
Therapeutic effects:
  • Treatment and prevention of deficiency states, particularly bone manifestations.
  • Improved calcium and phosphorous homeostasis in patients with chronic kidney disease.

Pharmacokinetics

Absorption: IV administration results in complete bioavailability; well absorbed following oral administration.

Distribution: Unknown.

Metabolism/Excretion: Converted by the liver to the active form of vitamin D2.

Half-Life: 32–37 hr (up to 96 hr).

Time/Action Profile

(effects on serum calcium)

ROUTEONSETPEAKDURATION
POunknown8 wk1 wk
IVunknown8 wk1 wk



Contraind./Precautions

Contraindicated in:

Use Cautiously in:

Adv. Reactions/Side Effects

Seen primarily as manifestations of toxicity (hypercalcemia)

CV: edema, arrhythmias, bradycardia, hypertension

Derm: pruritus

EENT: conjunctivitis, photophobia, rhinorrhea

F and E: hypercalcemia

GI: nausea, vomiting, liver enzymes, anorexia, constipation, dry mouth, metallic taste, PANCREATITIS, polydipsia, weight loss

GU: libido, albuminuria, azotemia, nocturia, polyuria

Metab: hyperthermia

MS: arthralgia, bone pain, metastatic calcification, muscle pain

Neuro: dizziness, headache, malaise, somnolence, weakness

Resp: dyspnea

Misc: HYPERSENSITIVITY REACTIONS (INCLUDING ANAPHYLAXIS, ANGIOEDEMA, HYPOTENSION, DYSPNEA, AND CARDIAC ARREST)

Interactions

Drug-drug:

Route/Dosage

Availability

(Generic available)

Assessment

Lab Test Considerations:

Toxicity and Overdose:

Implementation

Patient/Family Teaching

Evaluation/Desired Outcomes

US Brand Names

Hectorol, vitamin D2

Code

NDC Code