Product image of Kreon 25 000 (Pancreatin) supplied by GNH India

Kreon 25 000

Active Ingredient:
Pancreatin
Origin:
EU

Kreon 25 000 (Pancreatin)

Pancreatin, the active ingredient in Kreon 25 000, is a pancreatic enzyme preparation presented as 25000 USP lipase units per enteric‑coated capsule for oral use. It replaces deficient pancreatic enzymes and is used to manage exocrine pancreatic insufficiency in conditions such as cystic fibrosis, chronic pancreatitis, pancreatic cancer, and after pancreatic surgery.

GNH India supplies Kreon 25 000 as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Viatris Healthcare Sp. Z O.O.

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Indications & Clinical Uses

  • Kreon 25 000 provides pancreatic enzyme replacement for disorders that cause exocrine pancreatic insufficiency.
  • Cystic fibrosis: improves digestion and nutrient absorption by supplying missing lipase, amylase and protease.
  • Chronic pancreatitis: reduces steatorrhea and abdominal discomfort by supplementing pancreatic enzymes.
  • Pancreatic cancer: aids in maintaining caloric intake when tumor impairs pancreatic function.
  • Pancreatic resection: compensates for loss of pancreatic tissue after surgery, supporting normal digestion.

How It Works

  • Pancreatin contains a mixture of lipase, amylase and protease that are released in the small intestine after the enteric coating dissolves. These enzymes hydrolyze dietary fats, carbohydrates and proteins, thereby compensating for the reduced endogenous pancreatic secretion seen in exocrine pancreatic insufficiency and facilitating nutrient absorption.

Side Effects

Kreon 25 000 may cause gastrointestinal and hypersensitivity reactions.

Common Side Effects

  • Abdominal discomfort or cramping
  • Flatulence or bloating
  • Oily, foul‑smelling stools
  • Nausea or vomiting
  • Diarrhea
  • Mild abdominal pain

Serious or Rare Side Effects

  • Anaphylactic or severe allergic reaction
  • Acute pancreatitis exacerbation
  • Severe abdominal pain with vomiting
  • Intestinal obstruction or blockage
  • Stevens‑Johnson syndrome or severe skin rash
  • Hypersensitivity with respiratory distress

Precautions & Warnings

  • Before prescribing Kreon 25 000, consider the following safety measures.
  • Dose adjustment: required in patients with significant renal or hepatic impairment.
  • Monitoring: regularly assess nutritional status, weight gain and stool characteristics.
  • Allergy: avoid in individuals with known hypersensitivity to porcine proteins.
  • Pregnancy: safety not established; use only if potential benefit justifies the risk.
  • Drug interactions: antacids or acid‑suppressing agents may reduce enzyme activity.
  • Store at ambient temperature: keep in the original container, protect from moisture and heat.

Avoid Interactions

Kreon 25 000 can interact with other medications that affect gastric acidity or enzyme activity.

Major Interactions (Avoid)

  • Proton pump inhibitors: may reduce activation of enteric‑coated enzymes.
  • Antacids containing aluminum or magnesium: can bind enzymes and diminish efficacy.

Moderate Interactions (Monitor Closely)

  • Oral corticosteroids: may increase risk of gastrointestinal irritation.
  • Lipase inhibitors (e.g., orlistat): may compete for substrate and alter digestion.
  • Broad‑spectrum antibiotics: changes in gut flora could affect enzyme function.

Frequently Asked Questions

Kreon 25 000 is prescribed to replace missing pancreatic enzymes in patients with exocrine pancreatic insufficiency caused by conditions such as cystic fibrosis, chronic pancreatitis, pancreatic cancer, or after pancreatic surgery. By providing lipase, amylase and protease, it helps improve digestion and nutrient absorption.

Pancreatin is a blend of digestive enzymes that, once released from the enteric coating in the small intestine, hydrolyze dietary fats, carbohydrates and proteins. This compensates for the reduced endogenous pancreatic secretion, allowing the body to break down and absorb nutrients more effectively.

The specific dose of Kreon 25 000 is individualized by the prescribing clinician based on the patient’s degree of enzyme deficiency, dietary fat intake and clinical response. Dosage adjustments are made during follow‑up to achieve optimal digestive outcomes.

Safety data for Kreon 25 000 in 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 with 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.

Kreon 25 000 delivers a standardized 25000 USP lipase units per capsule and uses an enteric coating to protect enzymes from stomach acid. Compared with non‑coated formulations, it may provide more consistent enzyme release in the intestine, potentially improving fat digestion and reducing gastrointestinal side effects.

Kreon 25 000 should be stored at ambient temperature, below 25 °C, in its original packaging. Protect the capsules from moisture, direct sunlight and excessive heat to maintain enzyme activity throughout the shelf life.

Kreon 25 000 is taken orally, usually with meals or snacks that contain fat. The enteric‑coated capsules should be swallowed whole with a glass of water; they should not be crushed, chewed or opened, as this could damage the protective coating.

Serious risks include severe allergic reactions such as anaphylaxis, exacerbation of pancreatitis, and rare cases of intestinal obstruction. Patients should seek immediate medical attention if they experience symptoms like difficulty breathing, severe abdominal pain, or persistent vomiting.

Kreon 25 000 is contraindicated in individuals with a known hypersensitivity to porcine-derived proteins or any component of the formulation. It should also be avoided in patients who have experienced severe allergic reactions to pancreatic enzyme preparations.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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