Article date: August 1996
By: K. M. KOCH, I. M. DAVIS, A. E. GOODING, Y. YIN, in Volume 42, Issue 2, pages 201-205
1The 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.
2Bismuth 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.
3The pharmacokinetics of ranitidine after administration of ranitidine bismuth citrate were dose‐proportional and consistent with previous observations for ranitidine administered alone.
4Ranitidine bismuth citrate was well‐tolerated in single oral doses of up to 1600 mg.
DOI: 10.1046/j.1365-2125.1996.03929.x
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