Rabies immunoglobulin (RIG) is a medication made up of antibodies against the rabies virus.[10] It is used to prevent rabies following exposure.[10] It is given after the wound is cleaned with soap and water or povidone-iodine and is followed by a course of rabies vaccine.[10] It is given by injection into the site of the wound and into a muscle.[10] It is not needed in people who have been previously vaccinated against rabies.[11]
Common side effects include pain at the site of injection, fever, and headache.[10] Severe allergic reactions such as anaphylaxis may rarely occur.[12] Use during pregnancy is not known to harm the baby.[10] It works by binding to the rabies virus before it can enter nerve tissue.[10] After the virus has entered the central nervous system, rabies immunoglobulin is no longer useful.[10]
The use of rabies immunoglobulin in the form of blood serum dates from 1891.[13] Use became common within medicine in the 1950s.[14] It is on the World Health Organization's List of Essential Medicines.[15] Rabies immunoglobulin is expensive and hard to come by in the developing world.[16] In the United States it is estimated to be more than US$1,000.00 per dose,[17] and around £600 in the United Kingdom.[18] It is made from the blood plasma of people or horses who have high levels of the antibody in their blood.[10][17] The horse version is less expensive but has a higher rate of side effects.[17][14]
Rabies immunoglobulin (RIG) is indicated for the passive, transient post-exposure prophylaxis of rabies infection, when given immediately after contact with a rabid or possibly rabid animal and in combination with a rabies vaccine.[19][20][1]
There are three versions of rabies immunoglobulin licensed and available in the US.[21] Imogam Rabies-HT is produced by Sanofi Pasteur.[6] Kedrab is produced by Kedrion Biopharma.[19][7] Hyperrab is produced by Grifols.[8]
Imogam Rabies-HT and Kedrab have a nominal potency of 150 IU/mL while Hyperrab has a nominal potency of 300 IU/mL and requires smaller dosing. All three versions are used for post-exposure[22] and indicate local infusion at the wound site with additional amount intramuscularly at a site distant from vaccine administration.[23]
Kamrab is approved for medical use in Australia.[1]
^World Health Organization (2019). World Health Organization model list of essential medicines: 21st list 2019. Geneva: World Health Organization. hdl:10665/325771. WHO/MVP/EMP/IAU/2019.06. License: CC BY-NC-SA 3.0 IGO.
^Tintinalli JE (2010). Emergency Medicine: A Comprehensive Study Guide (Emergency Medicine (Tintinalli)) (7 ed.). New York: McGraw-Hill Companies. p. 1054. ISBN978-0-07-148480-0.