Anthrax Vaccine Adsorbed Dosage

Medically reviewed by Drugs.com. Last updated on Dec 6, 2021.

Usual Adult Dose for Anthrax Prophylaxis

Pre-Exposure Prophylaxis:
Primary series: 0.5 mL intramuscularly at 0, 1, and 6 months
Booster series: 0.5 mL intramuscularly 6 and 12 months after primary series and at 12-month intervals thereafter

Pre-Exposure Prophylaxis in patients at risk of hematoma from intramuscular injection:
Primary series: 0.5 mL subcutaneously at 0, 2, and 4 weeks and 6 months
Booster series: 0.5 mL subcutaneously 6 and 12 months after primary series and at 12-month intervals thereafter

Post-Exposure Prophylaxis:
Primary series: 0.5 mL subcutaneously at 0, 2, and 4 weeks post-exposure combined with antimicrobial therapy

Comments:

• Efficacy for post-exposure prophylaxis is based solely on animal models of inhalation anthrax.
• The optimal catch up schedule for missed or delayed booster doses is unknown.

Uses:

• Active immunization of patients aged 18 to 65 for pre-exposure prophylaxis in those at high risk of exposure
• Active immunization of patients aged 18 to 65 for post-exposure prophylaxis after suspected or confirmed Bacillus anthracis exposure, administered in conjunction with recommended antibacterials

Renal Dose Adjustments

Data not available

Liver Dose Adjustments

Data not available

Precautions

CONTRAINDICATIONS:

• Severe hypersensitivity (e.g. anaphylaxis) to any of the ingredients

Safety and efficacy have not been established in patients younger than 18 years or older than 65 years; this drug is not recommended for use in these patients.

To report suspected adverse reactions, contact the Vaccine Adverse Event Reporting System (VAERS) at: https://vaers.hhs.gov

Consult WARNINGS section for additional precautions.

Dialysis

Data not available

Other Comments

Administration advice:

• Administer pre-exposure prophylaxis intramuscularly into the deltoid or subcutaneously over the deltoid.
• Administer post-exposure prophylaxis subcutaneously over the deltoid.
• The vial stopper contains natural rubber latex which can cause allergic reactions in patients sensitive to latex.

Storage requirements:

• Refrigerate; do not freeze

Reconstitution/preparation techniques:

• Shake thoroughly to ensure a homogenous suspension during withdrawal.

IV compatibility:

• Do not mix with other products in the syringe

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer