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. 2011 Oct;43(7):1389-93.
doi: 10.1007/s11250-011-9866-5. Epub 2011 Apr 19.

Evaluation of the brain, renal, and hepatic effects of flunixin meglumine, ketoprofen, and phenylbutazone administration in Iranian fat-tailed sheep

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Evaluation of the brain, renal, and hepatic effects of flunixin meglumine, ketoprofen, and phenylbutazone administration in Iranian fat-tailed sheep

Ali Asghar Mozaffari et al. Trop Anim Health Prod. 2011 Oct.

Abstract

Purpose: The purpose of this study was to evaluate the brain, renal, and hepatic effects of three NSAIDs (flunixin meglumine, ketoprofen, and phenylbutazone) when administered IV to clinically normal Iranian fat-tailed sheep.

Methods: The experiments were conducted on twenty clinically normal adult female sheep. Sheep were randomly assigned to four groups: saline (n = 5), flunixin meglumine (n = 5), ketoprofen (n = 5), and phenylbutazone (n = 5). Drug administration was initiated at 8 AM: on day 1 and continued every 12 h for 12 days. Flunixin meglumine, ketoprofen, and phenylbutazone were administered at dose rate of 2.2, 4, and 4 mg/kg, respectively. Daily blood and urine samples were collected from all sheep for hematologic, enzymes activity, and urinalysis. Immediately after euthanasia, complete necropsy was performed on all sheep and gross lesions were recorded.

Results: Clinical, hematological, serum, and urine analysis and histopatholgical findings were described.

Conclusion: When the use of these compounds is contemplated in clinical cases, the risk of adverse effects and the comparative toxic potential should be considered, along with the efficacy of the compound for the condition being treated.

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References

    1. Vet Pathol. 1983 Nov;20(6):662-9 - PubMed
    1. Am J Med. 1985 Jun;78(6 Pt 1):992-1000 - PubMed
    1. J Am Vet Med Assoc. 1983 Feb 1;182(3):263-6 - PubMed
    1. Jpn J Cancer Res. 1995 Mar;86(3):252-63 - PubMed
    1. Vet Rec. 1979 Jul 14;105(2):26-30 - PubMed

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