Literature DB >> 3604253

The bioavailability of phenylbutazone in the horse.

P B Smith, J Caldwell, R L Smith, M W Horner, M S Moss.   

Abstract

[phenyl-14C]-Phenylbutazone was administered to 2 horses p.o. and i.v. on separate occasions. Plasma levels and urinary and faecal elimination of 14C were monitored for up to 7 days after dosing. Phenylbutazone was rapidly and extensively absorbed after oral administration, and its bioavailability was 91% assessed by comparison of plasma AUCs of unchanged drug after p.o. and i.v. administration. The plasma elimination half-life of phenylbutazone was 9.7 h and this was independent of the route of administration. The pattern of elimination of phenylbutazone was independent of the route of administration, with 55% of the dose being found in the urine in 3 days and a further 39% in the faeces in 7 days. These data, which are the first reports of the absolute bioavailability and excretion pathways of phenylbutazone in the horse, are discussed in terms of their significance for the gastrointestinal toxicity of this drug.

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Year:  1987        PMID: 3604253     DOI: 10.3109/00498258709043950

Source DB:  PubMed          Journal:  Xenobiotica        ISSN: 0049-8254            Impact factor:   1.908


  1 in total

1.  Ultrasonographic renal changes associated with phenylbutazone administration in three foals.

Authors:  R Léveillé; T Miyabayashi; S E Weisbrode; D S Biller; M Takiguchi; J F Williams
Journal:  Can Vet J       Date:  1996-04       Impact factor: 1.008

  1 in total

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