section name header

Pronunciation

da-KAR-ba-zeen

Classifications

Therapeutic Classification: antineoplastics

Pharmacologic Classification: alkylating agents

Indications

High Alert


Action

  • Disrupts DNA and RNA synthesis (cell-cycle phase–nonspecific).
Therapeutic effects:
  • Death of rapidly growing tissue cells, especially malignant ones.

Pharmacokinetics

Absorption: IV administration results in complete bioavailability.

Distribution: Widely distributed to tissues; probably concentrates in liver; some CNS penetration.

Metabolism/Excretion: 50% metabolized by the liver, 50% excreted unchanged by the kidneys.

Half-Life: 5 hr ( in renal and hepatic impairment).

Time/Action Profile

(effects on blood counts)

ROUTEONSETPEAKDURATION
IV (WBCs)16–20 days21–25 days3–5 days
IV (platelets)unknown16 days3–5 days



Contraind./Precautions

Contraindicated in:

Use Cautiously in:

Adv. Reactions/Side Effects

Derm: alopecia, facial flushing, photosensitivity, rash

Endo: gonadal suppression

GI: anorexia, nausea, vomiting, diarrhea, HEPATIC NECROSIS, hepatic vein thrombosis

Hemat: anemia, leukopenia, thrombocytopenia

Local: pain at IV site, phlebitis at IV site, tissue necrosis

MS: myalgia

Neuro: facial paresthesia, malaise

Misc: ANAPHYLAXIS, fever, flu-like syndrome

Interactions

Drug-drug:

Route/Dosage

Malignant Melanoma

Hodgkin's Disease

Availability

Assessment

Lab Test Considerations:

Implementation

IV Administration:

Patient/Family Teaching

Evaluation/Desired Outcomes

Code

NDC Code