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dc.contributor.authorJuma, FD
dc.date.accessioned2013-06-11T08:15:04Z
dc.date.available2013-06-11T08:15:04Z
dc.date.issued1983
dc.identifier.citationEur J Clin Pharmacol. 1983;25(3):425-6en
dc.identifier.urihttp://hinari-gw.who.int/whalecomwww.ncbi.nlm.nih.gov/whalecom0/pubmed/6628532
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/31231
dc.description.abstractThe pharmacokinetics of pindolol was studied in 8 normal Africans following administration of a single oral 10 mg dose. The mean peak concentration was 30.2 +/- 5.0 ng X ml-1, the mean half-life (t1/2) of the elimination phase was 3.4 +/- 1.1 h, and the total body clearance was 628 +/- 13 ml X min-1. The apparent volume of distribution was 3.0 +/- 1.31 X kg-1. The values are the same as those reported in Europeans.en
dc.language.isoenen
dc.publisherUnivesity of Nairobien
dc.titlePharmacokinetics of pindolol in Kenyan Africans.en
dc.typeArticleen
local.publisherDepartment of Medicineen


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