Product image of Kreon (Pancreas Powder) supplied by GNH India

Kreon

Active Ingredient:
Pancreas Powder
Origin:
EU

Kreon (Pancreas Powder)

Pancreas Powder, the active ingredient in Kreon, is a pancreatic enzyme preparation presented as a powder for oral use. It treats exocrine pancreatic insufficiency in patients with cystic fibrosis, chronic pancreatitis, and related digestive disorders.
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 Limited

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Indications & Clinical Uses

Kreon is a pancreatic enzyme preparation that supports digestion in conditions with impaired pancreatic function.

  • Exocrine pancreatic insufficiency: improves digestion of fats, proteins and carbohydrates in patients with insufficient pancreatic enzyme production.
  • Cystic fibrosis: provides necessary digestive enzymes to manage malabsorption associated with the disease.
  • Chronic pancreatitis: aids nutrient absorption by supplementing deficient pancreatic enzymes.

How It Works

  • Pancreas Powder contains a blend of lipases, proteases and amylases that replicate normal pancreatic secretions. After oral intake, the enteric‑coated formulation releases the enzymes in the duodenum, where they hydrolyze dietary triglycerides, proteins and starches, facilitating absorption of fatty acids, amino acids and glucose.

Side Effects

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

Common Side Effects

  • Abdominal discomfort or pain
  • Flatulence or gas
  • Oily or fatty stools (steatorrhea)
  • Nausea
  • Diarrhea
  • Constipation

Serious or Rare Side Effects

  • Allergic reactions including rash, itching or swelling
  • Anaphylaxis (severe allergic response)
  • Severe abdominal pain or pancreatitis exacerbation
  • Intestinal obstruction or blockage
  • Severe hypocalcemia due to fat malabsorption

Precautions & Warnings

Before prescribing Kreon, clinicians should consider several safety measures.

  • Dose adjustment: individualize based on clinical response and dietary fat intake.
  • Monitoring: regularly assess nutritional status, weight gain and stool characteristics.
  • Contraindications: avoid in patients with known hypersensitivity to porcine-derived enzymes.
  • Pregnancy and lactation: use only if clearly needed after risk‑benefit evaluation.
  • Drug interactions: be aware that antacids or proton‑pump inhibitors may reduce enzyme activity.
  • Store at room temperature below 25°C: keep in the original container, protect from moisture.

Avoid Interactions

Kreon can interact with other medicines, affecting its efficacy or safety.

Major Interactions (Avoid)

  • Antacids containing aluminum or magnesium: may inactivate pancreatic enzymes.
  • Proton‑pump inhibitors: can reduce enzyme activity by altering gastric pH.
  • Cholestyramine or other bile‑acid sequestrants: may bind enzymes and diminish effectiveness.

Moderate Interactions (Monitor Closely)

  • Oral corticosteroids: may increase risk of gastrointestinal irritation.
  • Broad‑spectrum antibiotics: alterations in gut flora could affect enzyme activity.
  • Warfarin: monitor INR as changes in fat absorption may influence vitamin K levels.

Frequently Asked Questions

Kreon is prescribed to patients with exocrine pancreatic insufficiency, including those with cystic fibrosis or chronic pancreatitis, to provide the digestive enzymes needed for the breakdown and absorption of fats, proteins and carbohydrates.

Pancreas Powder supplies lipases, proteases and amylases that mimic the body’s natural pancreatic secretions. After oral administration, the enzymes are released in the small intestine where they hydrolyze dietary nutrients, improving digestion and nutrient uptake.

The dose of Kreon is individualized and set by the prescribing clinician based on the patient’s weight, dietary fat intake and clinical response. No fixed regimen is provided in public information.

Limited clinical data are available for use during pregnancy or lactation. Kreon should be used only if the potential benefit justifies any possible risk to the mother or infant, and under medical supervision.

Enquiries are submitted via the product page on gnhindia.com, where the required quantity is entered. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Kreon contains a standardized mix of lipase, protease and amylase activities similar to other prescription pancreatic enzyme preparations. Differences may lie in enzyme potency, enteric coating technology and dosing flexibility, which clinicians consider when selecting therapy.

Store Kreon at room temperature below 25 °C, in the original packaging, and protect it from moisture. Do not expose the product to excessive heat or humidity, and keep it out of reach of children.

Kreon is taken orally, usually with meals or snacks that contain fat. The capsule or powder is swallowed whole or mixed with a small amount of acidic food, following the prescriber’s instructions for timing and dosage.

Serious risks include allergic reactions such as rash, swelling or anaphylaxis, severe abdominal pain that may indicate pancreatitis exacerbation, and rare cases of intestinal obstruction. Any of these symptoms require immediate medical attention.

Kreon should not be used by individuals with a known hypersensitivity to porcine-derived enzymes or any of the product’s excipients. Patients with severe gastrointestinal disorders that affect absorption may also be unsuitable candidates.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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