Drug Guide
Rabeprazole Sodium
Classification
Therapeutic: Gastroesophageal Reflux Disease (GERD), Zollinger-Ellison Syndrome, erosive esophagitis
Pharmacological: Proton pump inhibitor (PPI)
FDA Approved Indications
- Treatment of GERD
- Erosive esophagitis
- Zollinger-Ellison syndrome
Mechanism of Action
Rabeprazole irreversibly binds to the hydrogen-potassium ATPase enzyme system (the proton pump) in gastric parietal cells, inhibiting gastric acid secretion.
Dosage and Administration
Adult: 20 mg once daily before a meal; dosage may vary based on condition.
Pediatric: Not generally recommended for children under 18 years without specific indication.
Geriatric: Use with caution; adjust dose based on functional renal status.
Renal Impairment: Adjust dose if severe renal impairment.
Hepatic Impairment: No specific adjustment recommended; use caution.
Pharmacokinetics
Absorption: Rapidly absorbed, peak plasma levels in 2-5 hours.
Distribution: Widely distributed; plasma protein binding approximately 97%.
Metabolism: Primarily hepatic, via CYP2C19 and CYP3A4 enzymes.
Excretion: Metabolites excreted mainly in urine and feces.
Half Life: Approximately 1-2 hours.
Contraindications
- Hypersensitivity to rabeprazole or other PPIs.
Precautions
- Use with caution in patients taking concomitant medications that may increase risk of intestinal infections, osteoporosis, or vitamin B12 deficiency. Long-term use may increase risk of fractures, hypomagnesemia, and clostridium difficile-related diarrhea.
Adverse Reactions - Common
- Headache (Common)
- Nausea (Common)
- Diarrhea (Common)
- Abdominal pain (Common)
Adverse Reactions - Serious
- Clostridioides difficile-associated diarrhea (Less common)
- Severe skin reactions, including Stevens-Johnson syndrome (Rare)
- Interstitial nephritis (Rare)
Drug-Drug Interactions
- Clopidogrel: May reduce effectiveness; avoid use together or monitor carefully.
- Diazepam: Increased sedation potential.
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor for relief of GERD symptoms, and watch for adverse reactions, especially in long-term therapy.
Diagnoses:
- Risk for diarrhea related to altered gastric flora.
- Impaired gastrointestinal nutrition related to nausea or abdominal discomfort.
Implementation: Administer before meals, and instruct patients on proper use of sprinkle capsules if indicated.
Evaluation: Assess symptom relief and adverse effects regularly.
Patient/Family Teaching
- Take medication as directed, preferably before meals.
- Report persistent or severe side effects, including diarrhea or rash.
- Do not crush or chew delayed-release capsules.
- Maintain adequate calcium and vitamin D intake to prevent osteoporosis.
Special Considerations
Black Box Warnings:
- Long-term use may increase risk of fractures, hypomagnesemia, and Clostridioides difficile infection.
Genetic Factors: Cytochrome P450 2C19 polymorphisms may affect metabolism.
Lab Test Interference: Proton pump inhibitors may interfere with serum magnesium, calcium, B12, and gastric pH testing.
Overdose Management
Signs/Symptoms: Nausea, vomiting, dizziness, and abdominal pain.
Treatment: Supportive care, gastric lavage if recent ingestion, and monitoring of electrolytes; no specific antidote.
Storage and Handling
Storage: Store at room temperature, 20°C to 25°C (68°F to 77°F); keep in original container.
Stability: Stable for the duration specified on the package.