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Ranitidine upon meal‐induced gastric secretion: oral pharmacokinetics and plasma concentration effect relationships.
Author(s) -
Mig M,
Chau NP,
NguyenPhuoc BK,
Sauvage M,
Leguy F,
Bonfils S
Publication year - 1982
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 - 10.1111/j.1365-2125.1982.tb01960.x
Subject(s) - ranitidine , meal , pharmacokinetics , oral administration , medicine , gastric acid , gastric emptying , endocrinology , gastrin , chemistry , placebo , pharmacology , dose–response relationship , stomach , secretion , alternative medicine , pathology
1 Ranitidine oral kinetics and plasma concentration‐effect relationships upon meal‐induced gastric secretion were investigated in normal subjects. Four oral doses of ranitidine (50, 100, 150 or 200 mg) and placebo were tested. 2 Oral ranitidine showed a terminal half‐life of about 2 h 25 min. Maximal plasma level was about 240 ng/ml for a 100 mg dose, and occurred about 1 h after dose. From the range of 50 to 200 mg dose, no indication of non‐linearity was observed in the drug kinetics. 3 Ranitidine administration resulted in a dose‐related reduction in meal‐stimulated acid secretion reaching, 46, 70, 82 and 92%, respectively. Mean ranitidine plasma concentrations producing 50 and 80% inhibition of acid secretion were 73 and 180 ng/ml, respectively, with great inter‐individual variability. 150 and 200 mg ranitidine oral doses maintained IC50 for at least 4.5 and 5.5 h, respectively. Upon oral administration, ranitidine exerted no effect on gastric emptying of the meal but slightly decreased the gastrin response to the meal.