Product image of Lactulosum Aflofarm (Lactulose, Liquid) supplied by GNH India

Lactulosum Aflofarm

Active Ingredient:
Lactulose, Liquid
Origin:
EU

Lactulosum Aflofarm (Lactulose, Liquid)

Lactulose, the active ingredient in Lactulosum Aflofarm, is an osmotic laxative presented as a liquid solution for oral use. It treats constipation and hepatic encephalopathy in patients who require gentle bowel cleansing and ammonia reduction.
GNH India supplies Lactulosum Aflofarm as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Aflofarm Farmacja Polska Sp. Z O.O.

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Indications & Clinical Uses

Lactulose is used as an osmotic laxative and ammonia‑lowering agent in the following conditions:

  • Constipation: softens stool and promotes regular bowel movements.
  • Hepatic encephalopathy: lowers intestinal ammonia absorption, helping improve mental status.
  • Prevention of hepatic encephalopathy recurrence: maintains low ammonia levels to reduce the risk of episodic neurocognitive decline.

How It Works

  • Lactulose is a synthetic disaccharide that is not absorbed in the small intestine. In the colon it is metabolised by bacterial flora into short‑chain fatty acids, which increase the osmotic pressure within the lumen. This draws water into the colon, softening stool and stimulating peristalsis, while also converting ammonia to ammonium, reducing its systemic absorption and aiding patients with hepatic encephalopathy.

Side Effects

Lactulose may cause a range of adverse reactions, most of which are mild and transient.

Common Side Effects

  • Abdominal bloating: sensation of fullness or swelling in the abdomen.
  • Flatulence: increased intestinal gas production.
  • Diarrhoea: loose, watery stools, especially at higher doses.
  • Nausea: feeling of sickness or urge to vomit.
  • Abdominal cramping: painful muscle contractions in the gut.
  • Thirst: increased desire for fluids.

Serious or Rare Side Effects

  • Severe electrolyte imbalance: notably low potassium or sodium levels.
  • Dehydration: excessive fluid loss leading to dizziness or low blood pressure.
  • Allergic reaction: rash, itching, swelling, or difficulty breathing.
  • Severe abdominal pain: persistent, intense pain requiring medical evaluation.

Precautions & Warnings

Before initiating Lactulosum Aflofarm, consider the following safety measures:

  • Renal function assessment: evaluate kidney status to avoid accumulation.
  • Electrolyte monitoring: check serum potassium and sodium periodically.
  • Diabetes caution: monitor blood glucose as lactulose can affect carbohydrate metabolism.
  • Intestinal obstruction avoidance: do not use in patients with known blockage.
  • Hepatic impairment dose adjustment: consider lower doses in severe liver disease.
  • Store at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Lactulose can interact with other medicines; awareness of the interaction level helps manage risk.

Major Interactions (Avoid)

  • Antidiarrhoeal agents (e.g., loperamide): may counteract lactulose’s laxative effect.
  • Concurrent strong laxatives: increase risk of severe electrolyte disturbances.

Moderate Interactions (Monitor Closely)

  • Diabetes medications: lactulose may alter glucose control; monitor blood sugar.
  • Mineral supplements (e.g., magnesium): additive osmotic effect may enhance diarrhoea.
  • Oral antibiotics: may modify gut flora, potentially affecting lactulose metabolism.

Frequently Asked Questions

Lactulosum Aflofarm is a liquid formulation of lactulose used primarily to relieve constipation and to lower blood ammonia levels in patients with hepatic encephalopathy, helping to improve bowel regularity and mental function.

Lactulose is a synthetic sugar that reaches the colon unchanged, where gut bacteria ferment it into short‑chain fatty acids. This process raises the osmotic pressure in the intestinal lumen, drawing water into the colon to soften stool and also converting ammonia to ammonium, which is less readily absorbed.

The appropriate dose of Lactulosum Aflofarm is determined by the prescribing clinician based on the individual’s condition, age, renal function and response to therapy. Patients should follow the specific instructions provided by their healthcare professional.

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

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 and any necessary import documentation.

Lactulose is an osmotic laxative that works by increasing water content in the colon, whereas stimulant laxatives such as bisacodyl act by directly stimulating intestinal motility. Lactulose also has the unique benefit of reducing ammonia absorption, making it the preferred choice for patients with hepatic encephalopathy.

Lactulosum Aflofarm should be stored at ambient temperature, below 25 °C, in its original packaging to protect it from moisture and light. Ensure the container is tightly closed when not in use.

The product is taken orally as a liquid solution. It can be measured with a calibrated dosing device and swallowed directly or mixed with a small amount of water or juice, as directed by the prescribing clinician.

Serious risks include severe electrolyte imbalance, dehydration, and rare allergic reactions. Patients should be monitored for signs of excessive fluid loss, muscle weakness, or any hypersensitivity symptoms and seek medical attention promptly if they occur.

Lactulosum Aflofarm is contraindicated in individuals with known intestinal obstruction, perforation, or severe inflammatory bowel disease, and should be used with caution in patients with renal impairment or uncontrolled diabetes. A healthcare professional should evaluate suitability before prescribing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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