Interní Med. 2013; 15(5): 179-183
The introduction in the 1980s of proton pump inhibitors in the treatment of diseases, collectively referred to as gastric acid-related diseases,
became a major breakthrough in terms of treatment efficacy for these conditions. Currently, proton pump inhibitors are divided
into first-generation drugs (omeprazole, lansoprazole, pantoprazole) and second-generation drugs that include esomeprazole, the optical
isomer of omeprazole, and rabeprazole. Rabeprazole is the most recent of the proton pump inhibitors available at the Czech pharmaceutical
market. As other proton pump inhibitors, rabeprazole is safe and its advantage, in comparison with first-generation drugs, is
a rapid onset of suppression of gastric acid production and, thus, a rapid onset of improvement of clinical symptoms. The duration of
active suppression of gastric hydrochloric acid is long, lasting 14–16 hours, and the rate of side effects of treatment, such as headache
or diarrhea, is not higher than 1.6%. Clinical trials demonstrate a very good efficacy in persons with GERD; rabeprazole as part of H.
pylori eradication schedule is not superior to, for instance, the use of eradication schedule with omeprazole. A good therapeutic effect
has been described in the treatment of acute bleeding from ulcer lesions, primarily managed endoscopically, in which rabeprazole administered
orally was as effective as omeprazole given intravenously. Due to the differences of rabeprazole metabolism by cytochrome
P450 compared to other proton pump inhibitors, there are fewer drug interactions with rabeprazole. Rabeprazole is a drug with a high
therapeutic efficacy for diseases related to the presence of gastric hydrochloric acid.
Published: June 1, 2013 Show citation