The pharmacokinetics of ranitidine in patients with chronic duodenal ulceration: A comparison of responders and non-responders
Autor: | M. L. McFadyen, Raymond Miller, I. N. Marks, M. G. Moshal, Peter I. Folb |
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Rok vydání: | 1983 |
Předmět: |
Adult
Male medicine.medical_specialty Time Factors Cmax Administration Oral Ranitidine Gastroenterology Gastric Acid Cmin Pharmacokinetics Internal medicine Humans Medicine Infusions Parenteral Pharmacology (medical) Furans Pharmacology Volume of distribution business.industry Area under the curve General Medicine Middle Aged Anti-Ulcer Agents Bioavailability Kinetics Duodenal Ulcer Anesthesia Gastric acid Pentagastrin business medicine.drug |
Zdroj: | European Journal of Clinical Pharmacology. 24:441-447 |
ISSN: | 1432-1041 0031-6970 |
DOI: | 10.1007/bf00609883 |
Popis: | The pharmacokinetics of orally administered ranitidine were studied in 17 male patients with chronic duodenal ulceration. The patients were divided into 2 groups, 10 responders and 7 nonresponders, on the basis of their endoscopic response to ranitidine treatment. The 10 responders were studied both after a single 150 mg dose (SD) and after multiple dosing (MD) with ranitidine 150 mg twice daily for 4 weeks. The area under the curve (AUC) and maximum concentration (Cmax) were significantly higher (p less than 0.01 and p less than 0.05, respectively) after MD than after SD, but the half-life (t1/2) and minimum concentration (Cmin) 12 h postdosing did not differ. The non-responders were studied after MD only and their pharmacokinetic characteristics were compared with those of responders. No differences between the 2 groups were found. However, 2 non-responders had particularly low plasma ranitidine levels and high acid output. Such patients may need larger doses of ranitidine for adequate suppression of gastric acid. Five patients (4 responders and 1 non-responder) received ranitidine 20 mg i.v. The drug followed a two-compartment model, with mean values for t1/2 beta, volume of distribution steady-state and total plasma clearance of 80 min, 701 and 680 ml/min, respectively. The oral bioavailability of ranitidine in these 5 patients showed wide variation (27-76%; mean 51%). |
Databáze: | OpenAIRE |
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