DEXPURE TABLETS
DEXRABEPRAZOLE SODIUM
What it does
Dexrabeprazole is a medication that helps reduce stomach acid production.
Commonly used for: gastroesophageal reflux disease (GERD), stomach ulcers, esophagitis (inflammation of the esophagus)
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Source: Pharmacy and Poisons Board · fetched 2026-01-28 20:54:00 · updated 2026-07-26 11:44:32
About this medicine
Dexrabeprazole is a medication that helps reduce stomach acid production.
What it treats
- gastroesophageal reflux disease (GERD)
- stomach ulcers
- esophagitis (inflammation of the esophagus)
How it works
It works by blocking the pumps in the stomach that produce acid, helping to heal the stomach and relieve symptoms.
Who it's for
This medicine is for adults and children who need help with conditions caused by too much stomach acid.
AI-assisted summary grounded in BNF data - general information only, not medical advice. Always confirm with your pharmacist or doctor.
Clinical monograph: dexrabeprazole
BNF-referencedDexrabeprazole is a proton pump inhibitor (PPI) used primarily for the treatment of gastrointestinal disorders related to excess stomach acid. It is the active enantiomer of rabeprazole and works by reducing gastric acid secretion, thus providing relief from conditions such as gastroesophageal reflux disease (GERD) and peptic ulcers.
Indications
- Gastroesophageal reflux disease (GERD)
- Peptic ulcer disease
- Zollinger-Ellison syndrome
Dosage
Children: Refer to BNF for Children for specific dosing guidelines.
Adults: Refer to BNF for specific dosing guidelines.
Mechanism of action
Dexrabeprazole inhibits the hydrogen-potassium ATPase enzyme system (proton pump) at the secretory surface of the gastric parietal cells, leading to a profound and long-lasting reduction in gastric acid secretion.
Pharmacodynamics
As a PPI, dexrabeprazole effectively suppresses both basal and stimulated gastric acid secretion. The onset of action typically occurs within one hour of administration, with peak effects seen within two to four hours. The duration of acid suppression can last up to 24 hours, allowing for once-daily dosing.
Pharmacokinetics
Dexrabeprazole is rapidly absorbed after oral administration, with peak plasma concentrations occurring about one to four hours post-dose. It is extensively metabolized in the liver via cytochrome P450 enzymes, primarily CYP2C19 and CYP3A4. The elimination half-life is approximately one hour, with metabolites excreted primarily in urine.
Contra-indications
- Hypersensitivity to dexrabeprazole or any of its excipients
- Severe liver impairment
Adverse effects
- Headache
- Dizziness
- Nausea
- Diarrhoea
- Abdominal pain
- Constipation
- Flatulence
- Skin rash
- Elevated liver enzymes
Interactions
- May reduce the absorption of drugs requiring an acidic environment for absorption
- Increased risk of gastrointestinal infections with antibiotics
- May interact with anticoagulants and antiplatelet agents
Precautions
- Use with caution in patients with a history of liver disease
- Caution in patients with a known risk of Clostridium difficile infection
- Monitor for signs of hypomagnesemia
Pregnancy
The safety of dexrabeprazole in pregnancy has not been established. Use only if the potential benefit justifies the potential risk to the fetus.
Breast-feeding
It is not known whether dexrabeprazole is excreted in human milk. Caution should be exercised when administering to nursing women.
Storage
Store in a cool, dry place, away from direct sunlight. Keep out of reach of children.
Formulations
- Tablets
- Capsules
AI-synthesized from BNF references - general information only, not a substitute for professional medical advice or the current BNF. Verify doses with a pharmacist.
Molecular reference: dexrabeprazole
PubChem CID 9906855Molecular formula: C18H21N3O3S
Source: PubChem (NCBI) · pathways from PathBank, Reactome, WikiPathways & PharmGKB.
This drug in other countries
The same active ingredient registered across other registries we cover - including different brands.