Pharmacokinetics and bioequivalence testing of generic ondansetron preparations in healthy Thai male volunteers

Pharmacokinetics and bioequivalence of oral preparations of generic ondansetron were investigated in healthy Thai males. The test preparations were Vomitron 8 and Vomitron 4, the reference was Zofran. The three products were administered as an 8 mg single oral dose, in a three-period four-sequence c...

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Main Authors: Rojanasthien N., Manorot M., Kumsorn B.
Format: Clinical Trial
Language:English
Published: 2014
Online Access:http://www.ncbi.nlm.nih.gov/pubmed/3502482
http://cmuir.cmu.ac.th/handle/6653943832/3352
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Institution: Chiang Mai University
Language: English
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spelling th-cmuir.6653943832-33522014-08-30T02:26:02Z Pharmacokinetics and bioequivalence testing of generic ondansetron preparations in healthy Thai male volunteers Rojanasthien N. Manorot M. Kumsorn B. Pharmacokinetics and bioequivalence of oral preparations of generic ondansetron were investigated in healthy Thai males. The test preparations were Vomitron 8 and Vomitron 4, the reference was Zofran. The three products were administered as an 8 mg single oral dose, in a three-period four-sequence cross-over design with one-week washout period. An intravenous 8 mg Zofran was administered on the forth visit. Plasma ondansetron concentrations were determined by HPLC and the pharmacokinetic parameters were analyzed by non-compartmental analysis. 2014-08-30T02:26:02Z 2014-08-30T02:26:02Z 1999 Clinical Trial 0946-1965 10584976 http://www.ncbi.nlm.nih.gov/pubmed/3502482 http://cmuir.cmu.ac.th/handle/6653943832/3352 eng
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description Pharmacokinetics and bioequivalence of oral preparations of generic ondansetron were investigated in healthy Thai males. The test preparations were Vomitron 8 and Vomitron 4, the reference was Zofran. The three products were administered as an 8 mg single oral dose, in a three-period four-sequence cross-over design with one-week washout period. An intravenous 8 mg Zofran was administered on the forth visit. Plasma ondansetron concentrations were determined by HPLC and the pharmacokinetic parameters were analyzed by non-compartmental analysis.
format Clinical Trial
author Rojanasthien N.
Manorot M.
Kumsorn B.
spellingShingle Rojanasthien N.
Manorot M.
Kumsorn B.
Pharmacokinetics and bioequivalence testing of generic ondansetron preparations in healthy Thai male volunteers
author_facet Rojanasthien N.
Manorot M.
Kumsorn B.
author_sort Rojanasthien N.
title Pharmacokinetics and bioequivalence testing of generic ondansetron preparations in healthy Thai male volunteers
title_short Pharmacokinetics and bioequivalence testing of generic ondansetron preparations in healthy Thai male volunteers
title_full Pharmacokinetics and bioequivalence testing of generic ondansetron preparations in healthy Thai male volunteers
title_fullStr Pharmacokinetics and bioequivalence testing of generic ondansetron preparations in healthy Thai male volunteers
title_full_unstemmed Pharmacokinetics and bioequivalence testing of generic ondansetron preparations in healthy Thai male volunteers
title_sort pharmacokinetics and bioequivalence testing of generic ondansetron preparations in healthy thai male volunteers
publishDate 2014
url http://www.ncbi.nlm.nih.gov/pubmed/3502482
http://cmuir.cmu.ac.th/handle/6653943832/3352
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