{{Short description|Chemical compound}} {{cs1 config|name-list-style=vanc|display-authors=6}} {{Drugbox | Verifiedfields = changed | verifiedrevid = 448113917 | IUPAC_name = ''N''-(2-bromo-6-fluorophenyl)-4,5-dihydro-1''H''-imidazol-2-amine | image = Romifidine.svg | image_class = skin-invert-image

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<!--Pharmacokinetic data--> | bioavailability = | protein_bound = | metabolism = | elimination_half-life = | excretion =

<!--Identifiers--> | CAS_number_Ref = {{cascite|correct|??}} | CAS_number = 65896-16-4 | ATCvet = yes | ATC_prefix = N05 | ATC_suffix = CM93 | PubChem = 71969 | DrugBank_Ref = {{drugbankcite|correct|drugbank}} | DrugBank = | UNII_Ref = {{fdacite|correct|FDA}} | UNII = 876351L05K | ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}} | ChemSpiderID = 64975

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'''Romifidine''' is a drug that is used in veterinary medicine as a sedative mainly in large animals such as horses,<ref>{{cite journal | vauthors = Spadavecchia C, Arendt-Nielsen L, Andersen OK, Spadavecchia L, Schatzmann U | title = Effect of romifidine on the nociceptive withdrawal reflex and temporal summation in conscious horses | journal = American Journal of Veterinary Research | volume = 66 | issue = 11 | pages = 1992–1998 | date = November 2005 | pmid = 16334961 | doi = 10.2460/ajvr.2005.66.1992 | doi-access = free }}</ref> although it may be used in a wide variety of species.<ref>{{cite journal | vauthors = De Lucas JJ, Rodríguez C, Marín M, González F, Ballesteros C, San Andrés MI | title = Pharmacokinetics of intramuscular ketamine in young ostriches premedicated with romifidine | journal = Journal of Veterinary Medicine. A, Physiology, Pathology, Clinical Medicine | volume = 54 | issue = 1 | pages = 48–50 | date = February 2007 | pmid = 17359455 | doi = 10.1111/j.1439-0442.2007.00910.x | doi-access = free }}</ref><ref>{{cite journal | vauthors = Belda E, Laredo FG, Escobar M, Soler M, Lucas X, Agut A | title = Sedative and cardiorespiratory effects of three doses of romifidine in comparison with medetomidine in five cats | journal = The Veterinary Record | volume = 162 | issue = 3 | pages = 82–87 | date = January 2008 | pmid = 18204032 | doi = 10.1136/vr.162.3.82 | s2cid = 41300654 }}</ref> It is not used in humans, but is closely related in structure to the commonly used drug clonidine.

Romifidine acts as an agonist at the α<sub>2</sub> adrenergic receptor subtype. Side effects can include bradycardia and respiratory depression. It is often used alongside other sedative or analgesic drugs such as ketamine or butorphanol.<ref>{{cite journal | vauthors = Corletto F, Raisis AA, Brearley JC | title = Comparison of morphine and butorphanol as pre-anaesthetic agents in combination with romifidine for field castration in ponies | journal = Veterinary Anaesthesia and Analgesia | volume = 32 | issue = 1 | pages = 16–22 | date = January 2005 | pmid = 15663735 | doi = 10.1111/j.1467-2995.2004.00184.x }}</ref><ref>{{cite journal | vauthors = Kerr CL, McDonell WN, Young SS | title = Cardiopulmonary effects of romifidine/ketamine or xylazine/ketamine when used for short duration anesthesia in the horse | journal = Canadian Journal of Veterinary Research | volume = 68 | issue = 4 | pages = 274–282 | date = October 2004 | pmid = 15581222 | pmc = 1111358 }}</ref> Yohimbine can be used as an antidote to rapidly reverse the effects. ==Use== Romifidine is licensed for cats and dogs in several countries. Romifidine is licensed for non-meat horses. Romifidine may produce less ataxia during standing sedation than other α<sub>2</sub>-adrenergic receptor agonists.<ref name="lamont"/> ==Pharmacology== Romifidine is an α<sub>2</sub>-adrenergic receptor agonist that binds at a ratio of 340:1 over the imidazoline receptor.<ref name="lamont">{{cite book | vauthors = Lamont LA, Creighton CM | veditors = Lamont L, Grimm K, Robertson S, Love L, Schroeder C | chapter = Sedatives and Tranquilizers | title = Veterinary Anesthesia and Analgesia, The 6th Edition of Lumb and Jones | date = 11 September 2024 | pages = 338–344 | isbn = 978-1-119-83027-6 | publisher = Wiley Blackwell }}</ref>

==Side effects== Romifidine administration in sheep activates pulmonary macrophages that damage the endothelium of capillaries and alveolar type I cells. This in turns causes alveolar haemorrhage and oedema causing hypoxaemia.<ref name="lamont" /><ref>{{cite journal | vauthors = CS C, OS A, WN M, WD B | title = Histopathologic alterations induced in the lungs of sheep by use of alpha2-adrenergic receptor agonists | journal = American Journal of Veterinary Research | volume = 60 | issue = 2 | pages = 154–161 | date = Feb 1999 | pmid = 10048544 | publisher = Am J Vet Res | doi = 10.2460/ajvr.1999.60.02.154 | issn = 0002-9645 }}</ref><ref>{{cite journal | vauthors = Celly C, McDONELL W, Young S, Black W | title = The comparative hypoxaemic effect of four α 2 adrenoceptor agonists (xylazine, romifidine, detomidine and medetomidine) in sheep | journal = Journal of Veterinary Pharmacology and Therapeutics | volume = 20 | issue = 6 | pages = 464–471 | date = 1997 | pmid = 9430770 | doi = 10.1046/j.1365-2885.1997.00097.x | issn = 0140-7783 | url = https://onlinelibrary.wiley.com/doi/10.1046/j.1365-2885.1997.00097.x | url-access = subscription }}</ref>

== References == {{reflist|2}}

{{Hypnotics and sedatives}} {{Adrenergic receptor modulators}}

Category:Analgesics Category:Alpha2-adrenergic agonists Category:Organobromides Category:Fluoroarenes Category:Anilines Category:Sedatives Category:Imidazolines

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