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10 Tablet(s) per strip

Generic Name: Pantoprazole Sodium

Category: Tag:



  • Gastric danger ought to be precluded. Consider Zn++ supplementation during IV treatment in patients who are inclined to Zn++ insufficiency. Pregnancy. Checking Parameters Monitor Mg levels preceding inception and intermittently during delayed use. Lactation: Not known whether pantoprazole is disseminated into bosom milk; not prescribed


  • Peptic ulcer sickness, H. pylori contamination, Gastro-oesophageal reflux illness, Zollinger-Ellison disorder, Oesophagitis, Acid-related dyspepsia, NSAID-related ulceration, ulcer impervious to H2 receptor adversaries, Gastrointestinal (GI) seeping from pressure, Prophylaxis for corrosive desire disorder during acceptance of sedation


  • Concomitant use w/ rilpivirine, atazanavir and nelfinavir. Lactation.


  • Adult: PO The typical suggested grown-up oral portion is 40 mg given once day by day, before breakfast. The span of treatment is extending from 2 two months. Peptic ulcer: 40 mg/day in the first part of the day. Span: Duodenal ulceration: 2-4 wk; Benign gastric ulceration: 4-8 wk. GERD: 40 mg tablet, when day by day in the first part of the day for 4 to about two months. In safe ulcers: 40 mg tablet, when day by day for about two months. Ulcers actuated by NSAIDs: 40 mg tablet once every day, in patients getting persistent treatment with NSAIDs. GI seeping from pressure or corrosive peptic maladies: Usual grown-up oral measurements, whenever required the dose might be expanded. H. pylori contamination: 40 mg twice day by day w/clarithromycin and either amoxicillin or metronidazole. Zollinger-Ellison disorder: 160 mg tablets for each day. When control of corrosive emission has been accomplished, the portion ought to be slowly decreased. Prophylaxis for corrosive yearning disorder during enlistment of sedation: 40-80 mg tablet ought to be given the prior night medical procedure and rehashed the morning of medical procedure. IV Zollinger-Ellison disorder and other hypersecretory states As Na salt: 80 mg/day. Max: 240 mg/day in isolated portions if fast control required. GERD; Peptic ulcer As Na salt: 40 mg/day until PO can be continued. Upkeep treatment Maintenance treatment ought to include the most minimal portion of the medication. Both 20 and 40 mg dosages of Pantoprazole are sheltered and compelling in keeping up patients with mended reflux esophagitis and PUD abating. Senior patient: No issues with Pantoprazole have been experienced in clinical use right now.

Common Side Effects:

  • 1-10% Headache (>4%),Abdominal pain (4%),Facial edema (<4%),Generalized edema (<2%),Chest pain (4%),Diarrhea (4%),Constipation (<4%),Pruritus (4%),Rash (4%),Flatulence (<4%),Hyperglycemia (1%),Nausea (1%),Vomiting (>4%),Photosensitivity (<2%) Frequency Not Defined Angioedema,Atrophic gastritis,Anterior ischemic optic neuropathy,Hepatocellular damage leading to hepatic failure,Interstitial nephritis,Pancreatitis,Pancytopenia,Rhabdomyolysis,Risk of anaphylaxis,Stevens-Johnson syndrome,Fatal toxic epidermal necrolysis,Erythema multiforme

Mode Of Action:

  • Pantoprazole is a substituted benzimidazole, and also known as PPI due to its property to block the final step of acid secretion by inhibiting H+/K+ ATPase enzyme system in gastric parietal cell. Both basal and stimulated acid are inhibited.


  • Expanded danger of digoxin-initiated cardiotoxic impacts. Expanded danger of hypomagnesaemia w/diuretics. May build INR and prothrombin time of warfarin. May expand serum convergence of methotrexate and saquinavir. Deferred ingestion and diminished bioavailability w/sucralfate. Diminished assimilation of ketoconazole, itraconazole. Conceivably Fatal: May diminish serum levels and pharmacological impacts of rilpivirine, atazanavir and nelfinavir.

Pregnancy Interaction:

  • Pregnancy Category – B Animal reproduction studies have failed to demonstrate a risk to the fetus and there are no adequate and well-controlled studies in pregnant women OR Animal studies have shown an adverse effect, but adequate and well-controlled studies in pregnant women have failed to demonstrate a risk to the fetus in any trimester.

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