Paricel 10 mg (Tablet (Enteric Coated))
Unit Price: ৳ 3.51 (10 x 10: ৳ 351.00)
Strip Price: ৳ 35.10
Medicine Details
Category | Details |
---|---|
Generic | Rabeprazole sodium |
Company | Aci limited |
Also available as |
Indications
- Treatment of active duodenal ulcer
- Treatment of active benign gastric ulcer
- Treatment of symptomatic erosive or ulcerative gastro-esophageal reflux disease (GERD)
- Gastro-esophageal Reflux Disease Long-term Management (GERD Maintenance)
- Symptomatic treatment of moderate to very severe gastro-esophageal reflux disease (symptomatic GERD)
- Treatment of Zollinger-Ellison Syndrome
- In combination with antibacterial therapeutic regimens for the eradication of Helicobacter pylori
Pharmacology
- Suppresses gastric acid secretion by inhibiting the gastric H+/K+-ATPase
Dosage
- Recommended oral dose for active duodenal ulcer and active benign gastric ulcer is 20 mg once daily in the morning
- Recommended oral dose for erosive or ulcerative gastro-esophageal reflux disease (GERD) is 20 mg once daily for four to eight weeks
- Maintenance dose of rabeprazole sodium 20 mg or 10 mg once daily for long-term management of GERD
- Treatment of GERD in pediatric patients 1 to 11 years of age: 5 mg or 10 mg once daily for 12 weeks
- Starting dose of 60 mg once a day for Zollinger-Ellison Syndrome
- Combination therapy for H. pylori eradication: Rabeprazole sodium 20 mg twice daily for 7 days
Administration
- Tablets to be taken in the morning before eating
- Should be swallowed whole and not chewed or crushed
Interaction
- May interact with compounds whose absorption is pH dependent
- Co-administration with ketoconazole or itraconazole may decrease antifungal plasma levels
- No interaction with liquid antacids observed
- Not recommended to be co-administered with atazanavir
Contraindications
- Hypersensitivity to the active substance or excipients
- Contra-indicated in pregnancy and during breastfeeding
Side Effects
- May cause headache, diarrhea, abdominal pain, vomiting, constipation, dry mouth, changes in appetite, muscle pain, drowsiness, and dizziness
Pregnancy & Lactation
- US FDA pregnancy category 'C'
- Insufficient data for pregnant women, likely excreted in human milk
Precautions & Warnings
- Possibility of gastric or esophageal malignancy should be excluded prior to commencement of treatment
- Regular surveillance for patients on long-term treatment
- Possible increase in bone fracture risk in the elderly or with long-term use
- Risk of cross-hypersensitivity reactions with other proton pump inhibitors
- Caution for patients with osteoporosis and hypomagnesaemia
- Risk of gastrointestinal infections such as Salmonella, Campylobacter, and Clostridium difficile
- Interference with investigations for neuroendocrine tumors
- Consideration for vitamin B12 absorption and subacute cutaneous lupus erythematosus (SCLE)
- No dosage adjustment for patients with renal or hepatic impairment
Use in Special Populations
- No dosage adjustment necessary for patients with renal or hepatic impairment
- Not recommended for use in children due to lack of safety and efficacy data
Overdose Effects
- Maximum established exposure is 60 mg twice daily or 160 mg once daily
- Effects generally minimal and reversible without further medical intervention
Therapeutic Class
- Proton Pump Inhibitor
Storage Conditions
- Keep below 30°C, away from light and moisture, out of reach of children
Chemical Structure
- Molecular Formula: C18H21N3O3S
Common Questions
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