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Trade names | Imogam Rabies-HT, Kedrab, Hyperrab, others |
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Routes of administration | Intramuscular injection |
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Rabies immunoglobulin (RIG) is a medication made up of antibodies against the rabies virus.[9] It is used to prevent rabies following exposure.[9] It is given after the wound is cleaned with soap and water or povidone-iodine and is followed by a course of rabies vaccine.[9] It is given by injection into the site of the wound and into a muscle.[9] It is not needed in people who have been previously vaccinated against rabies.[10]
Common side effects include pain at the site of injection, fever, and headache.[9] Severe allergic reactions such as anaphylaxis may rarely occur.[11] Use during pregnancy is not known to harm the baby.[9] It works by binding to the rabies virus before it can enter nerve tissue.[9] After the virus has entered the central nervous system, rabies immunoglobulin is no longer useful.[9]
The use of rabies immunoglobulin in the form of blood serum dates from 1891.[12] Use became common within medicine in the 1950s.[13] It is on the World Health Organization's List of Essential Medicines.[14] Rabies immunoglobulin is expensive and hard to come by in the developing world.[15] In the United States it is estimated to be more than US$1,000.00 per dose.[16] It is made from the blood plasma of people or horses who have high levels of the antibody in their blood.[9][16] The horse version is less expensive but has a higher rate of side effects.[16][13]
Medical uses
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.[17][18][1]
Society and culture
Names
There are three versions of rabies immunoglobulin licensed and available in the US.[19] Imogam Rabies-HT is produced by Sanofi Pasteur.[5] Kedrab is produced by Kedrion Biopharma.[17][6] Hyperrab is produced by Grifols.[7]
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[20] and indicate local infusion at the wound site with additional amount intramuscularly at a site distant from vaccine administration.[21]
Kamrab is approved for medical use in Australia.[1]
References
- 1 2 3 4 "Kamrab". Therapeutic Goods Administration (TGA). 23 August 2021. Retrieved 10 September 2021.
- ↑ "Kamrab PI". Health Canada. 25 April 2012. Retrieved 10 September 2021.
- ↑ "Imogam PI". Health Canada. 25 April 2012. Retrieved 10 September 2021.
- ↑ "Hyperrab S/D PI". Health Canada. 25 April 2012. Retrieved 10 September 2021.
- 1 2 "Imogam Rabies-HT - human rabies virus immune globulin injection, solution". DailyMed. Retrieved 24 March 2020.
- 1 2 "Kedrab- human rabies virus immune globulin injection, solution". DailyMed. Retrieved 24 March 2020.
- 1 2 "Hyperrab (rabies immune globulin- human injection, solution". DailyMed. Retrieved 24 March 2020.
- ↑ "Hyperrab S/D (rabies immune globulin- human injection". DailyMed. Retrieved 10 September 2021.
- 1 2 3 4 5 6 7 8 9 "Rabies Immune Globulin". The American Society of Health-System Pharmacists. Archived from the original on 18 March 2011. Retrieved 8 January 2017.
- ↑ World Health Organization (2009). Stuart MC, Kouimtzi M, Hill SR (eds.). WHO Model Formulary 2008. World Health Organization. p. 398. hdl:10665/44053. ISBN 9789241547659.
- ↑ British national formulary : BNF 69 (69 ed.). British Medical Association. 2015. p. 869. ISBN 9780857111562.
- ↑ Rupprecht CE, Plotkin SA (2013). "Rabies Vaccines". In Plotkin SA, Orenstein WA, Offit PA (eds.). Vaccines (6th ed.). [Edinburgh]: Elsevier/Saunders. p. 659. ISBN 978-1455700905. Archived from the original on 9 January 2017.
- 1 2 Jong EC, Zuckerman JN (2004). Travelers' Vaccines. PMPH-USA. p. 205. ISBN 9781550092257. Archived from the original on 9 January 2017.
- ↑ 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. ISBN 978-0-07-148480-0.
- 1 2 3 Research Advances in Rabies. Academic Press. 2011. p. 351. ISBN 9780123870414. Archived from the original on 9 January 2017.
- 1 2 "Kedrab". U.S. Food and Drug Administration (FDA). 21 March 2018. Retrieved 7 June 2020. This article incorporates text from this source, which is in the public domain.
- ↑ "Summary Basis for Regulatory Action - Kedrab". FDA. 23 August 2017.
- ↑ "Vaccine and Immune Globulin Availability". Centers for Disease Control and Prevention (CDC). 26 February 2020. Retrieved 24 March 2020.
- ↑ "WHO Guide for Rabies Pre and Post Exposure Prophylaxis in Humans" (PDF). World Health Organization (WHO). 2014.
- ↑ "Rabies Biologics | Specific Groups | CDC". www.cdc.gov. 15 January 2021. Retrieved 18 November 2022.
Further reading
- Meeting of the Antimicrobial Drugs Advisory Committee (PDF) (Briefing Document). U.S. Food and Drug Administration (FDA). 25 April 2019.