section name header

Pronunciation

blee-oh-MYE-sin

Classifications

Therapeutic Classification: antineoplastics

Pharmacologic Classification: antitumor antibiotics

Indications

High Alert


Action

  • Inhibits DNA and RNA synthesis.
Therapeutic effects:
  • Death of rapidly replicating cells, particularly malignant ones.

Pharmacokinetics

Absorption: IV administration results in complete bioavailability. Well absorbed from IM and SUBQ sites. Absorption follows intrapleural and intraperitoneal administration.

Distribution: Widely distributed; concentrates in skin, lungs, peritoneum, kidneys, and lymphatics.

Metabolism/Excretion: 60–70% excreted unchanged by the kidneys.

Half-Life: 2 hr ( in renal impairment).

Time/Action Profile

(tumor response)

ROUTEONSETPEAKDURATION
IV, IM, SUBQ2–3 wkunknownunknown



Contraind./Precautions

Contraindicated in:

Use Cautiously in:

Adv. Reactions/Side Effects

CV: hypotension, peripheral vasoconstriction

Derm: hyperpigmentation, mucocutaneous toxicity, alopecia, erythema, rash, urticaria, vesiculation

GI: weight, anorexia, nausea, stomatitis, vomiting

Hemat: anemia, leukopenia, thrombocytopenia

Local: pain at tumor site, phlebitis at IV site

Neuro: aggressive behavior, disorientation, weakness

Resp: pneumonitis, PULMONARY FIBROSIS

Misc: chills, fever, ANAPHYLACTOID REACTIONS

Interactions

Drug-drug:

Route/Dosage

Availability

(Generic available)

Assessment

Lab Test Considerations:

Implementation

IV Administration:

Patient/Family Teaching

Evaluation/Desired Outcomes

Code

NDC Code