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Indications

REMS


Contraind./Precautions

Contraindicated in:

Use Cautiously in:

Adv. Reactions/Side Effects

Derm: pruritus, rash

MS: extremity pain

Neuro: drowsiness

Misc: HYPERSENSITIVITY REACTIONS (INCLUDING ANAPHYLAXIS), infusion reactions

Interactions

Drug-drug:

Availability

Route/Dosage

Action

  • A monoclonal antitoxin that blocks the activity of toxin produced by Bacillus anthracis. The toxin is a primary cause of disease progression.
Therapeutic effects:
  • Decreased morbidity and mortality associated with inhalational anthrax exposure and disease.

Classifications

Therapeutic Classification: antidotes

Pharmacologic Classification: monoclonal anti-toxins

Pharmacokinetics

Absorption: IV administration results in complete bioavailability.

Distribution: Some tissue distribution.

Metabolism/Excretion: No renal clearance.

Half-Life: 20.4 days

Time/Action Profile

(plasma concentrations)

ROUTEONSETPEAKDURATION
IVrapidend of infusionunknown

Patient/Family Teaching

Pronunciation

rax-ee-BAK-ue-mab

Code

NDC Code