Product image of Kreon (Pancreatin) supplied by GNH India

Kreon

Active Ingredient:
Pancreatin
Origin:
EU

Kreon (Pancreatin)

Pancreatin, the active ingredient in Kreon, is a pancreatic enzyme presented as enteric‑coated capsules for oral use. It provides enzyme replacement therapy for patients with exocrine pancreatic insufficiency due to conditions such as cystic fibrosis, chronic pancreatitis, pancreatic cancer, or post‑pancreatectomy.

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

Manufacturer / TM Owner

Viatris Healthcare Gmbh

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Indications & Clinical Uses

Kreon is indicated for disorders of exocrine pancreatic function where digestive enzyme supplementation is required.

  • Exocrine pancreatic insufficiency due to cystic fibrosis: improves digestion and absorption of fats, carbohydrates and proteins.
  • Chronic pancreatitis: aids nutrient absorption and reduces steatorrhea.
  • Pancreatic cancer: supports digestive function when pancreatic tissue is compromised.
  • Post‑pancreatectomy pancreatic insufficiency: replaces missing pancreatic enzymes to maintain nutritional status.

How It Works

  • Pancreatin in Kreon contains lipase, amylase and protease enzymes that are protected by an enteric coating. The coating prevents degradation in the acidic stomach environment and releases the enzymes in the duodenum, where they hydrolyze dietary fats, carbohydrates and proteins, facilitating their absorption in patients with deficient endogenous pancreatic secretion.

Side Effects

Kreon may cause adverse reactions, most of which are mild and reversible.

Common Side Effects

  • Abdominal discomfort or pain
  • Flatulence or bloating
  • Oily or fatty stools (steatorrhea)
  • Nausea or dyspepsia
  • Constipation or diarrhea
  • Mild skin rash

Serious or Rare Side Effects

  • Severe allergic reactions such as rash, angioedema or anaphylaxis
  • Acute pancreatitis exacerbation
  • Intestinal obstruction or ileus
  • Persistent severe abdominal pain
  • Fecal incontinence
  • Severe vomiting or dehydration

Precautions & Warnings

Before initiating Kreon, consider the following precautions.

  • Dose adjustment: tailor the dose to the individual’s clinical response and nutritional needs.
  • Monitor nutritional status: regularly assess weight, growth and fat‑soluble vitamin levels.
  • Hypersensitivity: avoid use in patients with known allergy to pork proteins or other components of the formulation.
  • Intestinal obstruction: use with caution in patients with known gastrointestinal blockage.
  • Pregnancy and lactation: safety has not been established; use only if clearly needed.
  • Store at ambient temperature: keep in the original container, protect from moisture and heat.

Avoid Interactions

Kreon can interact with other medicines, requiring attention to avoid reduced efficacy or increased risk.

Major Interactions (Avoid)

  • Antacids or proton pump inhibitors: may raise gastric pH and impair enzyme activation.
  • Orlistat: can bind to pancreatic enzymes and diminish their digestive effect.
  • High‑dose antibiotics altering gut flora: may affect enzyme activity.

Moderate Interactions (Monitor Closely)

  • Warfarin: changes in vitamin K absorption could affect anticoagulation control.
  • Digoxin: altered intestinal absorption may modify serum levels.
  • Statins: potential changes in lipid absorption could influence drug efficacy.

Frequently Asked Questions

Kreon is prescribed to patients with exocrine pancreatic insufficiency, a condition where the pancreas does not produce enough digestive enzymes. It helps improve the breakdown and absorption of fats, carbohydrates, and proteins, reducing symptoms such as steatorrhea, abdominal discomfort, and malnutrition.

Pancreatin in Kreon contains a blend of lipase, amylase and protease enzymes. The enteric coating protects these enzymes from stomach acid, allowing them to be released in the small intestine where they act on dietary nutrients, facilitating their digestion and absorption.

The dose of Kreon is individualized and determined by the prescribing clinician based on the patient’s severity of enzyme deficiency, dietary fat intake, and clinical response. Patients should follow the specific dosing instructions provided by their healthcare professional.

Safety data for Kreon in pregnancy and lactation are limited. It should only be used if the potential benefit justifies any possible risk to the fetus or infant, and the decision should be made by a qualified healthcare provider.

To order Kreon, 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.

Kreon offers a high‑potency, enteric‑coated formulation that protects enzymes from gastric acid, ensuring release in the duodenum. Compared with non‑coated preparations, it may provide more consistent enzyme activity and better tolerability, especially in patients requiring higher enzyme doses.

Kreon should be stored at ambient temperature, below 25 °C, in its original blister pack or bottle. Keep the product away from moisture, direct sunlight and excessive heat to maintain the integrity of the enteric coating.

Kreon is taken orally, usually with the first bite of each main meal and snack. The enteric‑coated capsules should be swallowed whole with water; they should not be crushed, chewed or opened, as this would compromise the protective coating.

Serious risks include severe allergic reactions such as anaphylaxis, exacerbation of pancreatitis, intestinal obstruction, and persistent severe abdominal pain. Patients experiencing any of these symptoms should seek immediate medical attention.

Kreon is contraindicated in individuals with a known hypersensitivity to pork proteins or any other component of the formulation. It should also be avoided in patients with active intestinal obstruction or severe gastrointestinal disease until the condition is resolved.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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