

Author: Itoh H. Nagano T. Hayashi T. Takeyama M.
Publisher: Pharmaceutical Press
ISSN: 1460-8081
Source: Pharmacy and Pharmacology Communications, Vol.6, Iss.11, 2000-11, pp. : 495-500
Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.
Abstract
The effect of the histamine H2 receptor antagonist, ranitidine, on plasma concentrations of acetaminophen was investigated with respect to hepatic metabolism, in five volunteers. Acetaminophen (1000 mg) together with ranitidine (300 mg), placebo or at 1 h after ranitidine (300 mg) was orally administered to five healthy male volunteers. Venous blood samples were taken before and after drug administration. Plasma acetaminophen and acetaminophen conjugates (glucuronide and sulphate) were determined by HPLC. The pharmacokinetic parameters were calculated from the plasma acetaminophen concentration–time curves from each volunteer. The area under the plasma acetaminophen concentration–time curve from 0 to 3 h (AUC0–3) significantly (
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