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# Antirabies Vaccine
## Overview
Antirabies vaccine is used for pre-exposure prophylaxis and post-exposure prophylaxis (PEP) to prevent rabies infection.
## Primary Indications
* **Pre-exposure prophylaxis (PrEP):** For individuals with increased risk of exposure to rabies virus (e.g., veterinarians, animal handlers, travelers to endemic areas).
* **Post-exposure prophylaxis (PEP):** Following potential rabies virus exposure in conjunction with rabies immune globulin (RIG) for unvaccinated individuals, or without RIG for previously vaccinated individuals.
## Adult Dosing
* **PrEP:**
* Intramuscular (IM): 1 mL on days 0, 7, and 21 (or 28). A booster dose is not routinely recommended for immunocompetent individuals but may be considered based on continued risk or serologic testing.
* Intradermal (ID): 0.1 mL at three different sites on days 0, 7, and 21 (or 28). This is an alternative regimen where locally available and cost-effective.
* **PEP (Unvaccinated individuals):**
* IM: 1 mL on days 0, 3, 7, 14, and 28. Administer RIG on day 0.
* ID: 0.1 mL at two different sites on days 0, 3, 7, and 28. Administer RIG on day 0.
* **PEP (Previously vaccinated individuals):**
* IM: 1 mL on days 0 and 3.
* ID: 0.1 mL at two different sites on days 0 and 3.
* RIG is NOT indicated for previously vaccinated individuals.
## Pediatric Dosing
Pediatric dosing is generally the same as adult dosing **by weight, not by age**. The standard 1 mL IM dose or 0.1 mL ID dose is used.
## Dose Adjustments
No dose adjustments are needed for renal or hepatic impairment. Dose depends on exposure risk and vaccination history.
## Contraindications
* Severe, life-threatening allergic reaction (anaphylaxis) to a previous dose of rabies vaccine or any component of the vaccine.
* Severe (anaphylactic) hypersensitivity to components of the vaccine (e.g., neomycin, streptomycin, amphotericin B when used in production).
## Adverse Effects
Common: Headache, fatigue, muscle aches, nausea, dizziness, abdominal pain, joint pain. Local reactions at the injection site (redness, swelling, pain, itching).
Less Common: Hives, joint swelling, fever, enlarged lymph nodes.
Rare: Severe allergic reactions. Neurologic events are exceedingly rare.
## Key Drug Interactions
* **Immunosuppressants:** May reduce the immune response to rabies vaccine. If concurrent therapy is unavoidable, assess antibody titers and consider administering additional doses. Steroids >20 mg/day prednisone equivalent for >14 days can interfere.
* **Antimalarials (e.g., chloroquine, mefloquine):** May reduce antibody response to intradermal rabies vaccine. IM vaccination should be used if antimalarials are necessary.
## Monitoring
* **PrEP:** Antibody titers are not routinely required but can be considered to assess response, especially in immunocompromised individuals or those with ongoing risk.
* **PEP:** Clinical assessment for signs and symptoms of rabies. Wound care. Documentation of vaccine and RIG administration.
## Clinical Pearls
* Rabies vaccine is highly effective when administered correctly, but **rabies immune globulin (RIG) is crucial for unvaccinated individuals receiving PEP**. RIG should be infiltrated around the wound as much as possible and the remainder given intramuscularly.
* Washing the wound thoroughly with soap and water is the **first and most critical step** in rabies PEP.
* The choice between IM and ID administration for PEP may vary based on local protocols and resource availability. While ID offers potential cost savings, IM is generally considered more reliable.
* Consult the most current CDC guidelines or local public health protocols for definitive recommendations on PEP, especially regarding the type of animal involved and its health status.
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**Disclaimer:** This information is intended for healthcare professionals and is not a substitute for professional medical advice. Always consult the current prescribing information and local protocols for definitive guidance.