Proton Pump Inhibitor

The gastric H+/K+-ATPase at the secretory surface of the stomach parietal cell is inhibited by rabeprazole, which reduces gastric acid secretion. It has been said that Rabeprazole acts as an inhibitor of the gastric proton pump since this enzyme is thought to be the acid (proton) pump within the parietal cell.

Duodenal ulcer: Rabeprazole 20 mg in the morning for 4 weeks. Most patients heal within 4 weeks.Healing of erosive or ulcerative Gastroesophageal Reflux Disease (GERD): Rablet 20 mg daily in the morning for 4 to 8 weeks. Those patients who have not healed after 8 weeks of treatment, an additional 8-week course of Rabeprazole may be considered.Treatment of symptomatic GERD: The recommended adult oral dose of Rabeprazole is 20 mg once daily in the morning for 4 weeks. If symptoms do not resolve completely after 4 weeks, an additional course of treatment may be considered.Maintenance of healing of erosive or ulcerative GERD: The recommended adult oral dose of Rabeprazole is 20 mg once daily. Controlled studies do not extend beyond 12 months.Zollinger-Ellison Syndrome: The recommended adult oral starting dose is 60 mg once a day. Doses should be adjusted according to individual patient needs and should continue for as long as clinically indicated. Some patients may require divided doses. Doses up to 100 mg once daily and 60 mg twice daily have been administered.Helicobacter pylori eradication to reduce the risk of Duodenal Ulcer recurrence: Rabeprazole 20 mg, Amoxicillin 1000 mg, Clarithromycin 500 mg twice daily in the morning and evening with meals for 7 days

Significant and persistent inhibition of stomach acid output is brought about by respite. A compound whose absorption is pH-dependent may interact with another substance. Itraconazole or ketoconazole co-administration with Rabeprazole Sodium may cause a considerable drop in antifungal plasma levels. Consequently, when ketoconazole or itraconazole are used concurrently with Respite, individual patients may need to be watched to determine if a dosage adjustment is warranted. There was no apparent interaction with liquid antacids. Atazanavir is pH-dependently absorbed. As a result, PPIs, such as rabeprazole, shouldn't be taken alongside atazanavir.

Hypersensitivity to any excipient or active ingredient. The use of Rabeprazole Sodium during pregnancy and breastfeeding is not advised.

In both short- and long-term studies, Rabeprazole Sodium is generally well tolerated. In some cases, rabeprazole may result in headache, nausea, vomiting, constipation, dry mouth, increased or decreased appetite, muscle pain, sleepiness, and dizziness.

FDA pregnancy category "C" in the US. There is no proof that Rabeprazole affects fertility or causes harm to the fetus, according to studies done on animals. Nevertheless, there isn't any good, controlled research on pregnant women. Since that rabeprazole is probably excreted in human milk, a choice should be made regarding whether to stop breastfeeding or to stop the medication, taking into account the significance of the medication to the mother.

Before starting treatment with Rabeprazole Sodium Gastro-resistant Tablets, the risk of malignancy should be ruled out because the presence of stomach or oesophageal malignancy is not precluded by the symptomatic response to therapy with rabeprazole. Long-term patients should be regularly monitored, especially those who have been on medication for more than a year. Proton pump inhibitors, particularly when used in high dosages and for extended periods of time (>1 year), may slightly increase the risk of hip, wrist, and spine fracture, mostly in elderly patients or when other known risk factors are present. Proton pump inhibitors may raise the total risk of fracture by 10% to 40%, according to observational studies. Other risk factors could account for some of this increase. Individuals who are at risk for osteoporosis should be looked after and should consume enough calcium and vitamin D.

The highest exposure that has been determined has never gone above 60 mg twice daily or 160 mg once daily. Effects are often mild, typical of recognized adverse event profiles, and reversible without additional medical help. There is no known particular antidote. Due to its high protein binding, rabeprazole cannot be dialyzed. Treatment for overdose should be symptomatic, as with any overdose, and broad supportive techniques should be used.

Keep away from light and moisture at a temperature below 30°C. Keep out of children's reach.

Proton Pump Inhibitor

The gastric H+/K+-ATPase at the secretory surface of the stomach parietal cell is inhibited by rabeprazole, which reduces gastric acid secretion. It has been said that Rabeprazole acts as an inhibitor of the gastric proton pump since this enzyme is thought to be the acid (proton) pump within the parietal cell.

FDA pregnancy category "C" in the US. There is no proof that Rabeprazole affects fertility or causes harm to the fetus, according to studies done on animals. Nevertheless, there isn't any good, controlled research on pregnant women. Since that rabeprazole is probably excreted in human milk, a choice should be made regarding whether to stop breastfeeding or to stop the medication, taking into account the significance of the medication to the mother.