Furazolidone
Furazolidone is a nitrofuran antibacterial agent and monoamine oxidase inhibitor (MAOI).[1] It is marketed by Roberts Laboratories under the brand name Furoxone and by GlaxoSmithKline as Dependal-M.
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AHFS/Drugs.com | Micromedex Detailed Consumer Information |
Routes of administration | Oral-Local |
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ECHA InfoCard | 100.000.594 |
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Formula | C8H7N3O5 |
Molar mass | 225.16 g·mol−1 |
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Medical uses
Furazolidone has been used in human and veterinary medicine. It has a broad spectrum of activity being active against
- Gram positivei
- Gram negative
- Escherichia coli
- Salmonella dublin
- Salmonella typhimurium
- Shigella
- Protozoa
Use in humans
In humans it has been used to treat diarrhoea and enteritis caused by bacteria or protozoan infections, including traveler's diarrhoea, cholera and bacteremic salmonellosis.
From the early 1970's it has been used in China to treat peptic ulcers, where the mechanism is treatment of the causative Helicobacter pylori infection.[2] In 2002, a journal article suggested it's use in treatment of helicobacter pylori infections in children.[3]
Furazolidone has also been used for giardiasis (due to Giardia lamblia), amoebiasis and shigellosis also though it is not a first line treatment.[4]
Use in animals
As a veterinary medicine, furazolidone has been used with some success to treat salmonids for Myxobolus cerebralis infections.
It has also been used in aquaculture.[5]
Since furazolidone is a nitrofuran antibiotic, its use in food animals is currently prohibited by the FDA under the Animal Medicinal Drug Use Clarification Act, 1994.[6]
Furazolidone is no longer available in the US.
Use in laboratory
It is used to differentiate micrococci and staphylococci.
Mechanism of action
It is believed to work by crosslinking of DNA.[7]
Side effects
Though an effective antibiotic when all others fail, against extremely drug resistant infections, it has many side effects. including inhibition of monoamine oxidase,[1] and as with other nitrofurans generally, minimum inhibitory concentrations also produce systemic toxicity: tremors, convulsions, peripheral neuritis, gastrointestinal disturbances, depression of spermatogenesis. Nitrofurans are recognized by FDA as mutagens/carcinogens, and can no longer be used since 1991.[8]
See also
References
- A.M. Timperio; H.A. Kuiper & L. Zolla (February 2003). "Identification of a furazolidone metabolite responsible for the inhibition of amino oxidases". Xenobiotica. 33 (2): 153–167. doi:10.1080/0049825021000038459. PMID 12623758. S2CID 35868007.
- Xiao, Shu Dong (2002). "How we discovered in China in 1972 that antibiotics cure peptic ulcer". In Barry J. Marshall (ed.). Helicobacter pioneers: first hand accounts from the scientists who discovered helicobacters, 1892–1982. Oxford: Blackwell. pp. 165–202. ISBN 978-0-86793-035-1.
- Machado RS, Silva MR, Viriato A (2008). "Furazolidone, tetracycline and omeprazole: a low-cost alternative for Helicobacter pylori eradication in children". Jornal de Pediatria. 84 (2): 160–5. doi:10.2223/JPED.1772. PMID 18372934.
- Petri WA (February 2005). "Treatment of Giardiasis". Curr Treat Options Gastroenterol. 8 (1): 13–17. doi:10.1007/s11938-005-0047-3. PMID 15625030. S2CID 22893579.
- Meng J, Mangat SS, Grudzinski IP, Law FC (1998). "Evidence of 14C-furazolidone metabolite binding to the hepatic DNA of trout". Drug Metabol Drug Interact. 14 (4): 209–19. doi:10.1515/DMDI.1998.14.4.209. PMID 10694929. S2CID 20792443.
- Bagley, Clell. "Drugs Prohibited from Extralabel Use in Animals". Retrieved 14 April 2014.
- "DrugBank: Showing Furazolidone (DB00614)". Retrieved 2008-12-19.
- "Untitled Document". caraga.da.gov.ph. Archived from the original on September 24, 2007.