Annals of Internal Medicine · 1983 · 48 citations · 10 references
MedicinePharmacologyPharmacotherapyClinical PharmacologyGastrointestinal PharmacotherapyPharmacovigilanceGastrointestinal PharmacologyPeptic Ulcer DiseasePeptic Ulcer PharmacotherapyAntihistamine PharmacologyGastric SecretionGastric Ulcer DiseaseHistamine H2 Receptor AntagonismHistamine ReceptorsHistamine-2 Receptor Antagonist TherapyHistamine-mediated SecretionZollinger-ellison Syndrome
Ranitidine, a new H2-receptor blocking antihistamine, is pharmacokinetically similar to cimetidine, but its potency is about eightfold greater. The clinical response to ranitidine is more prolonged, largely because of potency and not kinetic advantage. Increased potency has not meant greater clinical efficacy: duodenal ulcer healing, at 4, 6, or 8 weeks of therapy, does not differ between ranitidine and the cheaper cimetidine. Compliance and overall safety appear excellent for both drugs at this time. The safety record and side effects of cimetidine, but not ranitidine, are well established. So far, side effects of ranitidine are minimal, and in some cases anecdotal, but they cannot be ignored. Emerging information suggests that, although the incidence and severity of certain side effects may prove different for ranitidine than cimetidine, the pattern of side effects is similar with both drugs.
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Causes and characteristics of 500 consecutive cases of jaundice.
A Malchow-Møller, Peter Matzen, Beth Bjerregaard et al. · PubMed · 1981 · 119 citations
Cimetidine and ranitidine in duodenal ulcer.
M J Langman, David Henry, G B Bell et al. · BMJ · 1980 · 62 citations · Full text
Influence of ranitidine on plasma metoprolol and atenolol concentrations.
H. Spahn, E. Mutschler, Wilhelm Kirch et al. · BMJ · 1983 · 53 citations · Full text
High dose of antacid (Mylanta II) reduces bioavailability of ranitidine.
George W. Mihaly, Andrea Marino, Lorraine K. Webster et al. · BMJ · 1982 · 48 citations · Full text