Product image of Pantoprazol Stada (Pantoprazole Sodium Sesquihydrate) supplied by GNH India

Pantoprazol Stada

Active Ingredient:
Pantoprazole Sodium Sesquihydrate
Origin:
EU

Pantoprazol Stada (Pantoprazole Sodium Sesquihydrate)

Pantoprazole Sodium Sesquihydrate, the active ingredient in Pantoprazol Stada, is a proton pump inhibitor presented as a tablet for oral use. It reduces stomach acid production and is used to treat acid‑related disorders such as gastro‑oesophageal reflux disease and peptic ulcer disease in adults.

GNH India supplies Pantoprazol Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals and pharmacies worldwide.

Manufacturer / TM Owner

Stada Arzneimittel Ag

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Indications & Clinical Uses

Pantoprazol Stada is a proton pump inhibitor that acts on the gastric acid secretion pathway. It is indicated for several acid‑related conditions:

  • Gastro‑oesophageal reflux disease (GERD): provides symptomatic relief and promotes healing of erosive esophagitis.
  • Erosive oesophagitis: heals mucosal breaks caused by chronic acid exposure.
  • Peptic ulcer disease: supports ulcer healing and reduces risk of recurrence.
  • Zollinger‑Ellison syndrome: controls excessive gastric acid secretion in this rare endocrine disorder.

How It Works

  • Pantoprazole selectively and irreversibly binds to the H+/K+‑ATPase enzyme (the gastric proton pump) on the secretory surface of parietal cells. By inhibiting this final step of acid production, it markedly lowers gastric acidity, allowing damaged mucosa to heal and reducing acid‑related symptoms.

Side Effects

Pantoprazol Stada is generally well tolerated, but adverse reactions can occur.

Common Side Effects

  • Headache: mild to moderate intensity.
  • Diarrhoea: usually self‑limiting.
  • Nausea or abdominal discomfort.
  • Flatulence or bloating.
  • Constipation: occasional.
  • Dry mouth.

Serious or Rare Side Effects

  • Acute interstitial nephritis: presents with renal impairment and eosinophilia.
  • Severe hypersensitivity reactions: including Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Clostridioides difficile‑associated colitis: may cause severe diarrhoea.
  • Osteoporotic fractures: long‑term use linked to reduced bone mineral density.
  • Hypomagnesemia: low serum magnesium with prolonged therapy.

Precautions & Warnings

Before initiating therapy, consider the following precautions:

  • Assess renal function: dose adjustment may be required in severe impairment.
  • Review concomitant medications: potential for altered absorption of drugs that need an acidic environment.
  • Monitor for infection: prolonged acid suppression can increase risk of gastrointestinal infections.
  • Evaluate bone health: consider calcium and vitamin D supplementation for long‑term users.
  • Pregnancy and lactation: use only if clearly needed after risk‑benefit assessment.
  • Store at ambient temperature: keep below 25°C, retain in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Pantoprazole may affect the pharmacokinetics of several medicines. Awareness of the interaction potential helps optimise therapy.

Major Interactions (Avoid)

  • Antifungal agents (ketoconazole, itraconazole): reduced absorption and loss of efficacy.
  • HIV protease inhibitors (atazanavir, nelfinavir): markedly decreased plasma concentrations.

Moderate Interactions (Monitor Closely)

  • Clopidogrel: possible reduction in antiplatelet effect.
  • Warfarin: may enhance anticoagulant response, requiring INR monitoring.
  • Methotrexate (high dose): decreased renal clearance, risk of toxicity.
  • Digoxin: slight increase in serum levels.
  • Oral contraceptives: potential reduction in hormonal efficacy.

Frequently Asked Questions

Pantoprazol Stada contains pantoprazole, a proton pump inhibitor indicated for acid‑related disorders such as gastro‑oesophageal reflux disease, erosive oesophagitis, peptic ulcer disease and Zollinger‑Ellison syndrome. It works by reducing gastric acid secretion, which helps heal mucosal damage and relieves related symptoms.

Pantoprazole inhibits the H+/K+‑ATPase enzyme, commonly called the gastric proton pump, located on the secretory surface of parietal cells. By irreversibly blocking this final step of acid production, it lowers stomach acidity, allowing damaged tissue to repair and decreasing acid‑related discomfort.

The appropriate dose of Pantoprazol Stada is determined by the prescribing clinician based on the specific indication, severity of disease, and patient factors. Dosage regimens are individualized and should follow the prescriber’s instructions and local labeling.

Pantoprazole is classified as pregnancy category B in many regions, indicating no evidence of risk in animal studies but limited human data. It should be used during pregnancy or lactation only if clearly needed after a risk‑benefit assessment by the healthcare provider.

To request Pantoprazol Stada, 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 and any necessary import documentation.

Pantoprazol Stada is comparable to other PPIs such as omeprazole or esomeprazole in its ability to suppress gastric acid. Differences may include pharmacokinetic profiles, drug‑interaction potential, and specific regulatory approvals. Choice of agent often depends on clinician preference, patient tolerance and individual drug‑interaction considerations.

Pantoprazol Stada tablets should be stored at ambient temperature, below 25 °C. Keep the product in its original packaging, protect it from moisture and direct sunlight, and avoid storing in areas with high humidity or temperature fluctuations.

Pantoprazol Stada is supplied as oral tablets that are taken with water. It is usually administered once daily, preferably before a meal, but the exact timing and frequency should follow the prescribing clinician’s directions.

Serious risks, though uncommon, include acute interstitial nephritis, severe hypersensitivity reactions such as Stevens‑Johnson syndrome, Clostridioides difficile‑associated colitis, osteoporotic fractures with long‑term use, and hypomagnesemia. Patients should be monitored for these events, especially during prolonged therapy.

Pantoprazol Stada is contraindicated in patients with known hypersensitivity to pantoprazole or any component of the formulation. Caution is advised for individuals with severe liver impairment, those taking drugs that require an acidic environment for absorption, and patients with a history of certain infections or bone disorders.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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