Rabeprazole
- 1 January 1998
- journal article
- review article
- Published by Springer Nature in Drugs
- Vol. 55 (2) , 261-267
- https://doi.org/10.2165/00003495-199855020-00009
Abstract
▴ Rabeprazole is a proton pump inhibitor with anti-secretory properties. In vitro animal experiments have indicated that the inhibition of the proton pump by rabeprazole is partially reversible. ▴ Rabeprazole has 2- to 10-fold greater antisecretory activity than omeprazole in vitro. However, it dissociates more readily from H+,K+-ATPase than omeprazole, resulting in a shorter duration of action. ▴ In comparative clinical trials rabeprazole was significantly more effective than placebo, famotidine or ranitidine and as effective as omeprazole in the treatment of patients with erosive or ulcerative gastro-oesophageal reflux disease or gastric or duodenal ulcers. Healing rates with rabeprazole were independent of Helicobacter pylori status. ▴ Rabeprazole in combination with either clarithromycin and metronidazole or clarithromycin and amoxicillin or amoxicillin and metronidazole or clarithromycin for 7 days produced eradication of H. pylori in 100, 95, 90 and 63% of patients. ▴ The tolerability profile of rabeprazole 20mg once daily was similar to that of famotidine 20mg twice daily, ranitidine 150mg 4 times daily or omeprazole 20mg once daily in comparative trials. The adverse events reported with once daily administration of rabeprazole 20mg include malaise, nausea, diarrhoea, headache, dizziness and skin eruptions in 0.7 to 2.2% of patients.Keywords
This publication has 14 references indexed in Scilit:
- Effects of oral rabeprazole on oesophageal and gastric pH in patients with gastro‐oesophageal reflux diseaseAlimentary Pharmacology & Therapeutics, 1997
- Sites of Reaction of the Gastric H,K-ATPase with Extracytoplasmic Thiol ReagentsJournal of Biological Chemistry, 1997
- Kinectic Studies of Helicobacter pylori Urease Inhibition by a Novel Proton Pump Inhibitor, Rabeprazole.Biological & Pharmaceutical Bulletin, 1996
- Comparison of the kinetic disposition and metabolism of E3810, a new proton pump inhibitor, and omeprazole in relation to S-mephenytoin 4′-hydroxylation statusClinical Pharmacology & Therapeutics, 1995
- A proton pump inhibitor, E3810, has antibacterial activity through binding toHelicobacter pyloriThe Esophagus, 1995
- The proton pump inhibitor, E3810, binds to the N-terminal half of the α-subunit of gastric H+,K+-ATPaseBiochemical Pharmacology, 1995
- Specific proton pump inhibitors E3810 and lansoprazole affect the recovery process of gastric secretion in rats differentlyBiochemical Pharmacology, 1994
- Different biochemical modes of action of two irreversible H+,K(+)-ATPase inhibitors, omeprazole and E3810.Journal of Biological Chemistry, 1993
- Effects of Histamine H2-Receptor Antagonists and a Proton Pump Inhibitor on the Mucosal Hydroxyproline Content of Ethanol-HCI-lnduced Gastric Lesions in RatsDigestion, 1992
- The potency of substituted benzimidazoles such as E3810, omeprazole, RO 18-5364 to inhibit gastric H+,K+-ATPase is correlated with the rate of acid-activation of the inhibitorBiochemical Pharmacology, 1990