From Anvita Health Wiki
Indications
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Contraindications
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Dosage
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- A series of 3 injections is given 0.1 mL intradermally in deltoids on days 0, 7 & 28, or
- A series of 3 doses given 1 mL IM in deltoid on days 0, 7 & 21 or 28.
- Booster doses can be given every 2 years
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Pharmacokinetics
- after IM administration, antibody appears in the serum within 7-10 days & persists for at least 1 year
- elimination: liver
Monitor
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- swelling, erythema, itching, pain, local discomfort, nausea, headache, abdominal pain, muscle aches, dizziness, malaise, neuroparalytic reactions, hypersensitivity reactions
Drug-interactions
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Mechanism-of-action
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More General Terms
Additional Terms
References
- Saunders Manual of Medical Practice, Rakel (ed), WB Saunders, Philadelphia, 1996, pg 1171
- Kaiser Permanente Northern California Regional Drug Formulary, 1998
- Drug Information & Medication Formulary, Veterans Affairs, Central California Health Care System, 1st ed., Ravnan et al eds, 1998 - not on National VA formulary
- Anvita Health guideline :id 1101
- Rupprecht CE et al Use of a Reduced (4-Dose) Vaccine Schedule for Postexposure Prophylaxis to Prevent Human Rabies: Recommendations of the Advisory Committee on Immunization Practices MMWR March 19, 2010 / 59(02);1-9 <PubMed> PMID: [1] <Internet> [2]
- National Guideline Clearinghouse Use of a reduced (4-dose) vaccine schedule for postexposure prophylaxis to prevent human rabies: recommendations of the Advisory Committee on Immunization Practices (ACIP). ngc-guideline: [3]
human diploid cell rabies vaccine (Imovax, Imovax ID, HDCV)