Product image of Pantoprazole Inpharmatis (Pantoprazole) supplied by GNH India

Pantoprazole Inpharmatis

Active Ingredient:
Pantoprazole
Origin:
EU

Pantoprazole Inpharmatis (Pantoprazole)

Pantoprazole, the active ingredient in Pantoprazole Inpharmatis, is a proton pump inhibitor presented as an intravenous formulation for intravenous use. It treats acid‑related gastrointestinal conditions such as gastro‑oesophageal reflux disease, erosive esophagitis, peptic ulcer disease and is employed for stress‑ulcer prophylaxis in hospitalized patients across the EU market.

GNH India supplies Pantoprazole Inpharmatis as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

Inpharmatis Sia

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Indications & Clinical Uses

Pantoprazole is a proton pump inhibitor used to manage acid‑related gastrointestinal disorders.

  • Gastro‑oesophageal reflux disease (GERD): reduces gastric acid exposure, promoting symptom relief and mucosal healing.
  • Erosive esophagitis: facilitates healing of acid‑induced esophageal lesions.
  • Peptic ulcer disease: promotes ulcer resolution by suppressing acid secretion.
  • Stress ulcer prophylaxis: prevents stress‑related gastric mucosal injury in critically ill patients.

How It Works

  • Pantoprazole selectively and irreversibly inhibits the H+/K+ ATPase enzyme (gastric proton pump) located on the secretory surface of gastric parietal cells. By blocking this final step of acid production, it markedly reduces basal and stimulated gastric acid secretion, leading to increased gastric pH and allowing damaged mucosa to heal.

Side Effects

Pantoprazole is generally well tolerated, but adverse reactions can occur.

Common Side Effects

  • Headache: mild to moderate intensity.
  • Diarrhoea: usually transient.
  • Nausea: occasional and self‑limiting.
  • Abdominal pain: mild discomfort.
  • Flatulence: increased intestinal gas.
  • Injection site reactions: redness or mild irritation.

Serious or Rare Side Effects

  • Anaphylaxis: severe allergic reaction requiring immediate medical attention.
  • Clostridioides difficile infection: may occur with prolonged use.
  • Hypomagnesemia: low serum magnesium levels, especially with long‑term therapy.
  • Elevated liver enzymes: signs of hepatic stress.
  • Stevens‑Johnson syndrome/toxic epidermal necrolysis: rare severe skin reactions.
  • Cardiac arrhythmias: associated with electrolyte disturbances.

Precautions & Warnings

Before initiating therapy, clinicians should consider several safety measures.

  • Renal function assessment: adjust therapy in patients with impaired clearance.
  • Magnesium monitoring: check serum levels during prolonged treatment.
  • Hepatic impairment: use with caution in liver disease.
  • Elderly patients: start at lower doses and monitor response.
  • Drug interaction review: evaluate concomitant medications for potential interactions.
  • Store at room temperature: keep in original container, protect from moisture and light.

Avoid Interactions

Pantoprazole may interact with several medicines, requiring attention to the interaction severity.

Major Interactions (Avoid)

  • Clopidogrel: reduced antiplatelet effect, increasing cardiovascular risk.
  • Atazanavir: decreased absorption, compromising antiviral efficacy.
  • High‑dose methotrexate: increased toxicity due to reduced renal clearance.

Moderate Interactions (Monitor Closely)

  • Warfarin: possible alteration of INR, requiring more frequent monitoring.
  • Digoxin: potential increase in serum concentration.
  • Diazepam: enhanced sedative effect, necessitating dose adjustment.

Frequently Asked Questions

Pantoprazole Inpharmatis is an intravenous proton pump inhibitor indicated for the treatment of gastro‑oesophageal reflux disease, erosive esophagitis, peptic ulcer disease, and for the prevention of stress‑related gastric ulcers in hospitalized or critically ill patients.

Pantoprazole blocks the H+/K+ ATPase enzyme, also known as the gastric proton pump, on the surface of parietal cells. This inhibition stops the final step of gastric acid production, leading to a sustained increase in gastric pH and allowing acid‑related lesions to heal.

The specific dose and infusion rate are determined by the prescribing clinician based on the patient’s condition, severity, and renal or hepatic function. Standard dosing regimens exist, but the prescriber tailors therapy to each individual case.

Safety data for pantoprazole during pregnancy and lactation are limited. It should only be used when the potential benefit to the mother outweighs any possible risk to the fetus or infant, and the decision should be made by a qualified healthcare professional.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain if required) and necessary import documentation.

Pantoprazole shares the same mechanism of action as other proton pump inhibitors such as omeprazole or esomeprazole, but it is formulated for intravenous administration, offering rapid and reliable acid suppression in patients who cannot take oral medications. Its pharmacokinetic profile provides consistent plasma concentrations with a lower potential for drug‑drug interactions compared with some oral PPIs.

The product should be stored at room temperature, below 25 °C, in its original packaging to protect it from moisture and light. Once reconstituted, it must be used within the time frame specified in the product label and kept under aseptic conditions.

Pantoprazole Inpharmatis is given by intravenous infusion. The solution is added to a compatible diluent and administered over a period defined by the prescriber, typically 15–30 minutes, ensuring aseptic technique and proper line flushing before and after the infusion.

Serious risks include severe allergic reactions such as anaphylaxis, Clostridioides difficile‑associated diarrhoea, significant hypomagnesemia, liver enzyme elevations, and rare skin disorders like Stevens‑Johnson syndrome. Patients should be monitored for any signs of these conditions, and therapy should be discontinued if they occur.

Patients with known hypersensitivity to pantoprazole or any component of the formulation should avoid its use. Caution is also advised for individuals with severe hepatic impairment, those receiving certain interacting drugs (e.g., clopidogrel, atazanavir, high‑dose methotrexate), and patients with a history of severe allergic reactions to proton pump inhibitors.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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