Evaluation of the use of atropine sulfate, a combination of butylscopolammonium bromide and metamizole sodium, and flunixin meglumine to ameliorate clinical adverse effects of imidocarb dipropionate in horses
Objective—To evaluate the ability of atropine sulfate, butylscopolammonium bromide combined with metamizole sodium, and flunixin meglumine to ameliorate the clinical adverse effects of imidocarb dipropionate in horses. Animals—28 horses with piroplasmosis. Procedures—28 horses were randomly assigned...
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Veröffentlicht in: | American journal of veterinary research 2013-11, Vol.74 (11), p.1404-1408 |
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creator | Abutarbush, Sameeh M Alfaqeeh, Sameh M Mustafa, Ghazi Qura'n, Lara Al-Majali, Ahmad M |
description | Objective—To evaluate the ability of atropine sulfate, butylscopolammonium bromide combined with metamizole sodium, and flunixin meglumine to ameliorate the clinical adverse effects of imidocarb dipropionate in horses. Animals—28 horses with piroplasmosis. Procedures—28 horses were randomly assigned to 4 equal groups according to the pretreatment administered. Fifteen minutes before administration of 2.4 mg of imidocarb dipropionate/kg IM, horses in the first group were pretreated with 0.02 mg of atropine sulfate/kg IV, the second group with a combination of 0.2 mg of butylscopolammonium bromide/kg IV and 25 mg of metamizole sodium/kg IV, the third group with 1.1 mg of flunixin meglumine/kg IV, and the fourth (control) group with 1 mL of saline (0.9% NaCl) solution/50 kg IV. Physical examination, including evaluation of rectal temperature, heart and respiratory rates, capillary refill time, mucous membrane color, hydration status, abdominal sounds, signs of abdominal pain, salivation, diarrhea, and number of defecations, was performed. Results—Imidocarb dipropionate use in the control group was associated with serious adverse effects including signs of abdominal pain (4/7 horses) and diarrhea (2/7). Horses pretreated with atropine had no diarrhea, but 6 had signs of abdominal pain. Only 1 horse that received butylscopolammonium-metamizole pretreatment had signs of abdominal pain and 3 had diarrhea, which was numerically but not significantly different than the control group. Of horses pretreated with flunixin, 3 had signs of abdominal pain and 3 had diarrhea. Conclusions and Clinical Relevance—A combination of butylscopolammonium bromide and metamizole sodium may be useful to ameliorate the adverse effects of imidocarb dipropionate in horses, although group size was small and significant differences from the control group were not found. |
doi_str_mv | 10.2460/ajvr.74.11.1404 |
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Animals—28 horses with piroplasmosis. Procedures—28 horses were randomly assigned to 4 equal groups according to the pretreatment administered. Fifteen minutes before administration of 2.4 mg of imidocarb dipropionate/kg IM, horses in the first group were pretreated with 0.02 mg of atropine sulfate/kg IV, the second group with a combination of 0.2 mg of butylscopolammonium bromide/kg IV and 25 mg of metamizole sodium/kg IV, the third group with 1.1 mg of flunixin meglumine/kg IV, and the fourth (control) group with 1 mL of saline (0.9% NaCl) solution/50 kg IV. Physical examination, including evaluation of rectal temperature, heart and respiratory rates, capillary refill time, mucous membrane color, hydration status, abdominal sounds, signs of abdominal pain, salivation, diarrhea, and number of defecations, was performed. Results—Imidocarb dipropionate use in the control group was associated with serious adverse effects including signs of abdominal pain (4/7 horses) and diarrhea (2/7). Horses pretreated with atropine had no diarrhea, but 6 had signs of abdominal pain. Only 1 horse that received butylscopolammonium-metamizole pretreatment had signs of abdominal pain and 3 had diarrhea, which was numerically but not significantly different than the control group. Of horses pretreated with flunixin, 3 had signs of abdominal pain and 3 had diarrhea. Conclusions and Clinical Relevance—A combination of butylscopolammonium bromide and metamizole sodium may be useful to ameliorate the adverse effects of imidocarb dipropionate in horses, although group size was small and significant differences from the control group were not found.</description><identifier>ISSN: 0002-9645</identifier><identifier>EISSN: 1943-5681</identifier><identifier>DOI: 10.2460/ajvr.74.11.1404</identifier><identifier>PMID: 24168305</identifier><language>eng</language><publisher>United States</publisher><subject><![CDATA[Abdominal Pain - chemically induced ; Abdominal Pain - drug therapy ; Abdominal Pain - veterinary ; Administration, Intravenous - veterinary ; adverse effects ; Animals ; Anti-Inflammatory Agents, Non-Steroidal - administration & dosage ; Anti-Inflammatory Agents, Non-Steroidal - therapeutic use ; Antiprotozoal Agents - adverse effects ; atropine ; Atropine - administration & dosage ; Atropine - therapeutic use ; babesiosis ; Babesiosis - parasitology ; Babesiosis - veterinary ; body water ; Butylscopolammonium Bromide - administration & dosage ; Butylscopolammonium Bromide - therapeutic use ; clinical examination ; Clonixin - administration & dosage ; Clonixin - analogs & derivatives ; Clonixin - therapeutic use ; color ; diarrhea ; Diarrhea - chemically induced ; Diarrhea - drug therapy ; Diarrhea - veterinary ; Dipyrone - administration & dosage ; Dipyrone - therapeutic use ; Female ; flunixin ; group size ; heart ; Horse Diseases - chemically induced ; Horse Diseases - drug therapy ; Horse Diseases - parasitology ; horses ; Horses - metabolism ; imidocarb ; Imidocarb - adverse effects ; Imidocarb - analogs & derivatives ; Male ; mucosa ; Muscarinic Antagonists - administration & dosage ; Muscarinic Antagonists - therapeutic use ; pain ; respiratory rate ; salivation ; sodium chloride ; temperature]]></subject><ispartof>American journal of veterinary research, 2013-11, Vol.74 (11), p.1404-1408</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c387t-8b76ca85786f17752015b490361e5a376a48c6798ac13df502d58876c158c2063</citedby><cites>FETCH-LOGICAL-c387t-8b76ca85786f17752015b490361e5a376a48c6798ac13df502d58876c158c2063</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24168305$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Abutarbush, Sameeh M</creatorcontrib><creatorcontrib>Alfaqeeh, Sameh M</creatorcontrib><creatorcontrib>Mustafa, Ghazi</creatorcontrib><creatorcontrib>Qura'n, Lara</creatorcontrib><creatorcontrib>Al-Majali, Ahmad M</creatorcontrib><title>Evaluation of the use of atropine sulfate, a combination of butylscopolammonium bromide and metamizole sodium, and flunixin meglumine to ameliorate clinical adverse effects of imidocarb dipropionate in horses</title><title>American journal of veterinary research</title><addtitle>Am J Vet Res</addtitle><description>Objective—To evaluate the ability of atropine sulfate, butylscopolammonium bromide combined with metamizole sodium, and flunixin meglumine to ameliorate the clinical adverse effects of imidocarb dipropionate in horses. Animals—28 horses with piroplasmosis. Procedures—28 horses were randomly assigned to 4 equal groups according to the pretreatment administered. Fifteen minutes before administration of 2.4 mg of imidocarb dipropionate/kg IM, horses in the first group were pretreated with 0.02 mg of atropine sulfate/kg IV, the second group with a combination of 0.2 mg of butylscopolammonium bromide/kg IV and 25 mg of metamizole sodium/kg IV, the third group with 1.1 mg of flunixin meglumine/kg IV, and the fourth (control) group with 1 mL of saline (0.9% NaCl) solution/50 kg IV. Physical examination, including evaluation of rectal temperature, heart and respiratory rates, capillary refill time, mucous membrane color, hydration status, abdominal sounds, signs of abdominal pain, salivation, diarrhea, and number of defecations, was performed. Results—Imidocarb dipropionate use in the control group was associated with serious adverse effects including signs of abdominal pain (4/7 horses) and diarrhea (2/7). Horses pretreated with atropine had no diarrhea, but 6 had signs of abdominal pain. Only 1 horse that received butylscopolammonium-metamizole pretreatment had signs of abdominal pain and 3 had diarrhea, which was numerically but not significantly different than the control group. Of horses pretreated with flunixin, 3 had signs of abdominal pain and 3 had diarrhea. Conclusions and Clinical Relevance—A combination of butylscopolammonium bromide and metamizole sodium may be useful to ameliorate the adverse effects of imidocarb dipropionate in horses, although group size was small and significant differences from the control group were not found.</description><subject>Abdominal Pain - chemically induced</subject><subject>Abdominal Pain - drug therapy</subject><subject>Abdominal Pain - veterinary</subject><subject>Administration, Intravenous - veterinary</subject><subject>adverse effects</subject><subject>Animals</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - administration & dosage</subject><subject>Anti-Inflammatory Agents, Non-Steroidal - therapeutic use</subject><subject>Antiprotozoal Agents - adverse effects</subject><subject>atropine</subject><subject>Atropine - administration & dosage</subject><subject>Atropine - therapeutic use</subject><subject>babesiosis</subject><subject>Babesiosis - parasitology</subject><subject>Babesiosis - veterinary</subject><subject>body water</subject><subject>Butylscopolammonium Bromide - administration & dosage</subject><subject>Butylscopolammonium Bromide - therapeutic use</subject><subject>clinical examination</subject><subject>Clonixin - administration & dosage</subject><subject>Clonixin - analogs & derivatives</subject><subject>Clonixin - therapeutic use</subject><subject>color</subject><subject>diarrhea</subject><subject>Diarrhea - chemically induced</subject><subject>Diarrhea - drug therapy</subject><subject>Diarrhea - veterinary</subject><subject>Dipyrone - administration & dosage</subject><subject>Dipyrone - therapeutic use</subject><subject>Female</subject><subject>flunixin</subject><subject>group size</subject><subject>heart</subject><subject>Horse Diseases - chemically induced</subject><subject>Horse Diseases - drug therapy</subject><subject>Horse Diseases - parasitology</subject><subject>horses</subject><subject>Horses - metabolism</subject><subject>imidocarb</subject><subject>Imidocarb - adverse effects</subject><subject>Imidocarb - analogs & derivatives</subject><subject>Male</subject><subject>mucosa</subject><subject>Muscarinic Antagonists - administration & dosage</subject><subject>Muscarinic Antagonists - therapeutic use</subject><subject>pain</subject><subject>respiratory rate</subject><subject>salivation</subject><subject>sodium chloride</subject><subject>temperature</subject><issn>0002-9645</issn><issn>1943-5681</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kUFvFSEUhYnR2Nfq2p2ydNH3CgMMzNI0tZo0caFdkzsMtDQwPIF5sf5Kf5KMr3YF4X73nEMOQu8o2XW8JxfwcMg7yXeU7ign_AXa0IGzregVfYk2hJBuO_RcnKDTUh4IoZ2i4jU66TjtFSNig_5cHSAsUH2acXK43lu8FLteoea097PFZQkOqj3HgE2Ko5-f6XGpj6GYtE8BYkyzXyIec4p-shjmCUdbIfrfKTSRNLXp-b9nF5bZ__Jzm9-FJa4eNWGINviUmxM2wc_eQMAwHWxucaxz1tSyevqmngzkEU9-vyZM87rS1O5TQ8sb9MpBKPbt03mGbj9f_bj8sr35dv318tPN1jAl61aNsjeghFS9o1KKjlAx8oGwnloBTPbAlenloMBQNjlBukko1XaoUKYjPTtDH4-6LcTPxZaqoy_GhgCzTUvRlHPJh4EJ0dCLI2pyKiVbp_fZR8iPmhK91qjXGrXkmlK91tg23j-JL2O00zP_v7cGfDgCDpKGu-yLvv2-_qF1LPggGfsLSaenaQ</recordid><startdate>20131101</startdate><enddate>20131101</enddate><creator>Abutarbush, Sameeh M</creator><creator>Alfaqeeh, Sameh M</creator><creator>Mustafa, Ghazi</creator><creator>Qura'n, Lara</creator><creator>Al-Majali, Ahmad M</creator><scope>FBQ</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20131101</creationdate><title>Evaluation of the use of atropine sulfate, a combination of butylscopolammonium bromide and metamizole sodium, and flunixin meglumine to ameliorate clinical adverse effects of imidocarb dipropionate in horses</title><author>Abutarbush, Sameeh M ; Alfaqeeh, Sameh M ; Mustafa, Ghazi ; Qura'n, Lara ; Al-Majali, Ahmad M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c387t-8b76ca85786f17752015b490361e5a376a48c6798ac13df502d58876c158c2063</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Abdominal Pain - chemically induced</topic><topic>Abdominal Pain - drug therapy</topic><topic>Abdominal Pain - veterinary</topic><topic>Administration, Intravenous - veterinary</topic><topic>adverse effects</topic><topic>Animals</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - administration & dosage</topic><topic>Anti-Inflammatory Agents, Non-Steroidal - therapeutic use</topic><topic>Antiprotozoal Agents - adverse effects</topic><topic>atropine</topic><topic>Atropine - administration & dosage</topic><topic>Atropine - therapeutic use</topic><topic>babesiosis</topic><topic>Babesiosis - parasitology</topic><topic>Babesiosis - veterinary</topic><topic>body water</topic><topic>Butylscopolammonium Bromide - administration & dosage</topic><topic>Butylscopolammonium Bromide - therapeutic use</topic><topic>clinical examination</topic><topic>Clonixin - administration & dosage</topic><topic>Clonixin - analogs & derivatives</topic><topic>Clonixin - therapeutic use</topic><topic>color</topic><topic>diarrhea</topic><topic>Diarrhea - chemically induced</topic><topic>Diarrhea - drug therapy</topic><topic>Diarrhea - veterinary</topic><topic>Dipyrone - administration & dosage</topic><topic>Dipyrone - therapeutic use</topic><topic>Female</topic><topic>flunixin</topic><topic>group size</topic><topic>heart</topic><topic>Horse Diseases - chemically induced</topic><topic>Horse Diseases - drug therapy</topic><topic>Horse Diseases - parasitology</topic><topic>horses</topic><topic>Horses - metabolism</topic><topic>imidocarb</topic><topic>Imidocarb - adverse effects</topic><topic>Imidocarb - analogs & derivatives</topic><topic>Male</topic><topic>mucosa</topic><topic>Muscarinic Antagonists - administration & dosage</topic><topic>Muscarinic Antagonists - therapeutic use</topic><topic>pain</topic><topic>respiratory rate</topic><topic>salivation</topic><topic>sodium chloride</topic><topic>temperature</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Abutarbush, Sameeh M</creatorcontrib><creatorcontrib>Alfaqeeh, Sameh M</creatorcontrib><creatorcontrib>Mustafa, Ghazi</creatorcontrib><creatorcontrib>Qura'n, Lara</creatorcontrib><creatorcontrib>Al-Majali, Ahmad M</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of veterinary research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Abutarbush, Sameeh M</au><au>Alfaqeeh, Sameh M</au><au>Mustafa, Ghazi</au><au>Qura'n, Lara</au><au>Al-Majali, Ahmad M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of the use of atropine sulfate, a combination of butylscopolammonium bromide and metamizole sodium, and flunixin meglumine to ameliorate clinical adverse effects of imidocarb dipropionate in horses</atitle><jtitle>American journal of veterinary research</jtitle><addtitle>Am J Vet Res</addtitle><date>2013-11-01</date><risdate>2013</risdate><volume>74</volume><issue>11</issue><spage>1404</spage><epage>1408</epage><pages>1404-1408</pages><issn>0002-9645</issn><eissn>1943-5681</eissn><abstract>Objective—To evaluate the ability of atropine sulfate, butylscopolammonium bromide combined with metamizole sodium, and flunixin meglumine to ameliorate the clinical adverse effects of imidocarb dipropionate in horses. Animals—28 horses with piroplasmosis. Procedures—28 horses were randomly assigned to 4 equal groups according to the pretreatment administered. Fifteen minutes before administration of 2.4 mg of imidocarb dipropionate/kg IM, horses in the first group were pretreated with 0.02 mg of atropine sulfate/kg IV, the second group with a combination of 0.2 mg of butylscopolammonium bromide/kg IV and 25 mg of metamizole sodium/kg IV, the third group with 1.1 mg of flunixin meglumine/kg IV, and the fourth (control) group with 1 mL of saline (0.9% NaCl) solution/50 kg IV. Physical examination, including evaluation of rectal temperature, heart and respiratory rates, capillary refill time, mucous membrane color, hydration status, abdominal sounds, signs of abdominal pain, salivation, diarrhea, and number of defecations, was performed. Results—Imidocarb dipropionate use in the control group was associated with serious adverse effects including signs of abdominal pain (4/7 horses) and diarrhea (2/7). Horses pretreated with atropine had no diarrhea, but 6 had signs of abdominal pain. Only 1 horse that received butylscopolammonium-metamizole pretreatment had signs of abdominal pain and 3 had diarrhea, which was numerically but not significantly different than the control group. Of horses pretreated with flunixin, 3 had signs of abdominal pain and 3 had diarrhea. Conclusions and Clinical Relevance—A combination of butylscopolammonium bromide and metamizole sodium may be useful to ameliorate the adverse effects of imidocarb dipropionate in horses, although group size was small and significant differences from the control group were not found.</abstract><cop>United States</cop><pmid>24168305</pmid><doi>10.2460/ajvr.74.11.1404</doi><tpages>5</tpages></addata></record> |
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subjects | Abdominal Pain - chemically induced Abdominal Pain - drug therapy Abdominal Pain - veterinary Administration, Intravenous - veterinary adverse effects Animals Anti-Inflammatory Agents, Non-Steroidal - administration & dosage Anti-Inflammatory Agents, Non-Steroidal - therapeutic use Antiprotozoal Agents - adverse effects atropine Atropine - administration & dosage Atropine - therapeutic use babesiosis Babesiosis - parasitology Babesiosis - veterinary body water Butylscopolammonium Bromide - administration & dosage Butylscopolammonium Bromide - therapeutic use clinical examination Clonixin - administration & dosage Clonixin - analogs & derivatives Clonixin - therapeutic use color diarrhea Diarrhea - chemically induced Diarrhea - drug therapy Diarrhea - veterinary Dipyrone - administration & dosage Dipyrone - therapeutic use Female flunixin group size heart Horse Diseases - chemically induced Horse Diseases - drug therapy Horse Diseases - parasitology horses Horses - metabolism imidocarb Imidocarb - adverse effects Imidocarb - analogs & derivatives Male mucosa Muscarinic Antagonists - administration & dosage Muscarinic Antagonists - therapeutic use pain respiratory rate salivation sodium chloride temperature |
title | Evaluation of the use of atropine sulfate, a combination of butylscopolammonium bromide and metamizole sodium, and flunixin meglumine to ameliorate clinical adverse effects of imidocarb dipropionate in horses |
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