Product image of Laevolac (Lactulose) supplied by GNH India

Laevolac

Active Ingredient:
Lactulose
Origin:
EU

Laevolac (Lactulose)

Lactulose, the active ingredient in Laevolac, is an osmotic laxative presented as an oral solution for oral use. It is employed to relieve constipation and to prevent or treat hepatic encephalopathy in patients with liver disease. The solution is formulated to be palatable and is approved for distribution across the European Union, where it is commonly prescribed for gastrointestinal and hepatic indications.

GNH India supplies Laevolac as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies, transplant centres and oncology centres worldwide, ensuring quality and regulatory compliance for global markets.

Manufacturer / TM Owner

Ferraz Lynce, S.A.

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Indications & Clinical Uses

Laevolac (lactulose) acts as an osmotic laxative and ammonia‑lowering agent, addressing conditions related to bowel motility and hepatic ammonia accumulation.

  • Constipation: softens stool and increases bowel movements, providing relief from infrequent or difficult defecation.
  • Hepatic encephalopathy: reduces blood ammonia levels, helping to prevent or improve neuropsychiatric symptoms in patients with liver disease.
  • Hyperammonemia in liver disease: lowers systemic ammonia, supporting metabolic control in chronic liver conditions.

How It Works

  • Lactulose is a synthetic disaccharide that reaches the colon unchanged, where bacterial enzymes hydrolyze it to short‑chain fatty acids such as lactic and acetic acid. The resulting acidification lowers colonic pH, converting ammonia (NH3) to ammonium (NH4+), which is trapped in the lumen and excreted. The osmotic effect of the unabsorbed sugars also draws water into the bowel, softening stool and stimulating peristalsis.

Side Effects

Lactulose may cause gastrointestinal and metabolic reactions, ranging from mild to serious.

Common Side Effects

  • Flatulence: increased intestinal gas.
  • Abdominal cramps: intermittent stomach pain.
  • Diarrhea: loose stools, especially at higher doses.

Serious or Rare Side Effects

  • Electrolyte imbalance: notably low potassium.
  • Severe dehydration: from excessive fluid loss.
  • Allergic reaction: rash, itching, or swelling.

Precautions & Warnings

When prescribing Laevolac, clinicians should consider several safety measures to minimise risks.

  • Assess renal function: impaired kidneys may reduce lactulose clearance.
  • Monitor electrolytes: especially potassium, during prolonged therapy.
  • Use caution in diabetics: lactulose contains sugars that may affect glucose control.
  • Avoid in galactosemia: patients lack the ability to metabolise certain sugars.
  • Adjust dose in hepatic failure: severe liver dysfunction may require careful titration.
  • Store at room temperature: keep below 25°C in the original container, protect from moisture.

Avoid Interactions

Lactulose can influence the activity of other medicines, requiring attention to potential interactions.

Major Interactions (Avoid)

  • Antidiarrheal agents (e.g., loperamide): may counteract lactulose’s laxative effect.
  • Broad‑spectrum antibiotics: can alter colonic flora, reducing lactulose metabolism.
  • Oral phosphate binders: may bind lactulose, decreasing its efficacy.

Moderate Interactions (Monitor Closely)

  • Metformin: combined use may increase gastrointestinal discomfort.
  • Sucralfate: may decrease lactulose absorption if taken simultaneously.
  • Iron supplements: can reduce lactulose’s osmotic activity when co‑administered.

Frequently Asked Questions

Laevolac contains lactulose, which is used to treat constipation by softening stools and increasing bowel movements, and to prevent or manage hepatic encephalopathy by lowering blood ammonia levels in patients with liver disease.

Lactulose reaches the colon unchanged, where gut bacteria break it down into short‑chain acids that lower colonic pH. This acid environment converts ammonia to ammonium, trapping it in the lumen, while the osmotic effect draws water into the bowel, promoting stool softening and peristalsis.

The appropriate dose of Laevolac is determined by the prescribing clinician based on the individual’s condition, severity, and response. Dosage may be adjusted over time, and patients should follow the specific instructions provided by their healthcare professional.

Safety data for lactulose 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 in consultation with a qualified healthcare provider.

To order Laevolac, 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.

Unlike stimulant laxatives, lactulose works osmotically and also lowers ammonia levels, making it suitable for patients with liver disease. It is generally gentler on the bowel, but may cause more gas and bloating compared with bulk‑forming agents. Choice of therapy depends on the clinical situation and physician judgment.

Laevolac should be stored at room temperature, below 25 °C, in its original packaging to protect it from moisture and light. Keep the container tightly closed and out of reach of children. No refrigeration is required for this oral solution.

Laevolac is taken orally, usually as a measured dose of the liquid solution. It can be mixed with water or another non‑carbonated beverage to improve palatability. Patients should follow the administration instructions given by their prescriber or pharmacist.

Serious risks include electrolyte disturbances such as hypokalemia, severe dehydration from excessive diarrhea, and rare allergic reactions that may present as rash, itching or swelling. Prompt medical attention is required if any of these symptoms develop.

Laevolac is contraindicated in patients with known hypersensitivity to lactulose, those with galactosemia, and individuals with intestinal obstruction or severe bowel disease where increased motility could be harmful. Clinicians should also exercise caution in patients with renal impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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