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Pharmacokinetics of bismuth and ranitidine following single doses of ranitidine bismuth citrate
Author(s) -
KOCH K. M.,
DAVIS I. M.,
GOODING A. E.,
YIN Y.
Publication year - 1996
Publication title -
british journal of clinical pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.216
H-Index - 146
eISSN - 1365-2125
pISSN - 0306-5251
DOI - 10.1046/j.1365-2125.1996.03929.x
Subject(s) - ranitidine , pharmacokinetics , ranitidine hydrochloride , bismuth , pharmacology , oral administration , chemistry , absorption (acoustics) , medicine , materials science , organic chemistry , composite material
1 The pharmacokinetics of bismuth and ranitidine derived from ranitidine bismuth citrate given in single oral doses ranging from 200 mg to 1600 mg were evaluated in healthy subjects. 2 Bismuth was only minimally absorbed (<0.5% of the amount dosed) after administration of ranitidine bismuth citrate, and peak plasma concentrations never exceeded 33 ng ml −1 in any subject. Plasma concentrations and urinary recoveries of bismuth at doses up to and including 800 mg were relatively constant and not proportional to dose. Bismuth absorption was increased more than proportionally with the dose at 1600 mg. 3 The pharmacokinetics of ranitidine after administration of ranitidine bismuth citrate were dose‐proportional and consistent with previous observations for ranitidine administered alone. 4 Ranitidine bismuth citrate was well‐tolerated in single oral doses of up to 1600 mg.