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Finix 20
(Tablet)
Generics: Rabeprazole Sodium 20mg
Opsonin Pharma Ltd.
price/7.00 tk
Symptoms (Indications)
Rabeprazole is prescribed for duodenal ulcer healing, erosive or ulcerative Gastroesophageal Reflux Disease (GERD) healing, symptomatic GERD treatment, maintenance of healing of erosive or ulcerative GERD, Zollinger-Ellison Syndrome, and Helicobacter pylori eradication to reduce the risk of Duodenal Ulcer recurrence.
Pharmacology
Rabeprazole Sodium acts as a gastric proton-pump inhibitor, suppressing gastric acid secretion by inhibiting the gastric H+/K+-ATPase.
Dosage
The recommended dosage of Rabeprazole Sodium varies for different conditions: 20 mg once daily in the morning for active duodenal ulcer and active benign gastric ulcer, 20 mg once daily for 4-8 weeks for erosive or ulcerative GERD, 20 mg or 10 mg once daily for GERD maintenance depending on patient response, starting with a 60 mg once-daily dose for Zollinger-Ellison Syndrome and titrating upwards based on individual needs, and a combination therapy involving rabeprazole sodium 20 mg twice daily for 7 days for H. pylori eradication.
Administration
Should be taken in the morning before eating, and swallowed whole without chewing or crushing.
Interaction
Possible interaction with compounds pH-dependent absorption.
Co-administration with ketoconazole or itraconazole may decrease antifungal plasma levels.
Avoid co-administration with atazanavir.
Contraindications
Hypersensitivity to the active ingredient or any excipient.
Not recommended during pregnancy or nursing.
Side Effects
Generally well-tolerated; possible side effects include headache, diarrhea, abdominal discomfort, vomiting, constipation, dry mouth, increased or decreased appetite, muscle soreness, sleepiness, and dizziness.
Pregnancy & Lactation
FDA pregnancy category 'C'. Caution is advised during breastfeeding.
Precautions & Warnings
Symptomatic response does not exclude the presence of gastric or esophageal malignancy.
Regular surveillance for long-term treatment.
Risk of fractures, especially in the elderly.
Caution in patients with hepatic impairment.
Hypomagnesemia and interference with vitamin B12 absorption.
Subacute cutaneous lupus erythematosus (SCLE) association.
Interference with laboratory tests (Chromogranin A level).
Therapeutic Class
Proton Pump Inhibitor
Storage Conditions
Below 30°C, avoid direct sunlight, and keep away from children.
Pharmaceutical Name
Opsonin Pharma Ltd.
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