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

Lactulose Biogaran

Active Ingredient:
Lactulose, Liquid
Origin:
EU

Lactulose Biogaran (Lactulose, Liquid)

Lactulose, the active ingredient in Lactulose Biogaran, is an osmotic laxative presented as a liquid oral solution for oral use. It is indicated for the relief of constipation and for the reduction of ammonia absorption in patients with hepatic encephalopathy, primarily in adult populations.

GNH India supplies Lactulose Biogaran as a licensed, GDP‑compliant international pharmaceutical supplier, providing the product to hospitals, pharmacies and clinics worldwide with adherence to quality standards and regulatory requirements.

Manufacturer / TM Owner

Biogaran

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Indications & Clinical Uses

Lactulose is an osmotic laxative used to manage conditions related to bowel motility and hepatic ammonia accumulation.

  • Constipation: Provides osmotic activity that draws water into the colon, facilitating softer stools and regular bowel movements.
  • Hepatic encephalopathy: Reduces intestinal absorption of ammonia, helping to lower blood ammonia levels and improve neurological symptoms.
  • Prevention of hepatic encephalopathy recurrence: Maintains lower ammonia levels to reduce the risk of symptom relapse.

How It Works

  • Lactulose is a synthetic disaccharide that is not absorbed in the small intestine. In the colon, bacterial enzymes hydrolyze it to short‑chain fatty acids, which increase the osmotic pressure within the lumen, drawing water into the bowel and softening stool. The acidic environment also converts ammonia (NH3) to ammonium (NH4+), limiting its absorption and thereby decreasing systemic ammonia levels.

Side Effects

Lactulose may cause a range of adverse reactions, most of which are related to its osmotic activity in the gastrointestinal tract.

Common Side Effects

  • Abdominal bloating: Sensation of fullness or swelling in the abdomen.
  • Flatulence: Increased intestinal gas production.
  • Diarrhea: Loose, watery stools, especially at higher doses.
  • Nausea: Feeling of sickness or urge to vomit.
  • Abdominal cramps: Intermittent painful contractions of the gut.
  • Thirst: Increased desire for fluids.

Serious or Rare Side Effects

  • Severe electrolyte imbalance: Marked changes in sodium, potassium, or magnesium levels.
  • Dehydration: Significant loss of body water due to excessive diarrhea.
  • Allergic reaction: Rash, itching, swelling, or difficulty breathing.
  • Severe abdominal pain: Persistent, intense pain requiring medical evaluation.
  • Worsening hepatic encephalopathy: Unexpected deterioration of neurological status.

Precautions & Warnings

Before initiating Lactulose therapy, consider the following safety measures.

  • Assess renal function: Impaired kidneys may affect fluid and electrolyte balance.
  • Monitor electrolytes: Regular checks of sodium, potassium, and magnesium are advised.
  • Use caution in diabetes: Lactulose contains carbohydrate fragments that may affect glucose control.
  • Avoid abrupt discontinuation: Sudden stop may lead to rebound constipation.
  • Store at ambient temperature: Keep below 25 °C in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Lactulose can interact with other medications, altering efficacy or safety.

Major Interactions (Avoid)

  • Antibiotics such as rifaximin: May reduce Lactulose's effectiveness in lowering ammonia.
  • Magnesium‑containing laxatives: Additive osmotic effect can cause excessive diarrhea.
  • Diuretics: Increased risk of electrolyte disturbances.

Moderate Interactions (Monitor Closely)

  • Antacids containing aluminum or calcium: May bind Lactulose and diminish its activity.
  • Probiotics: May modify gut flora, potentially affecting Lactulose metabolism.
  • Oral hypoglycemic agents: Carbohydrate content of Lactulose could influence blood glucose levels.

Frequently Asked Questions

Lactulose Biogaran is used primarily to relieve constipation and to lower blood ammonia levels in patients with hepatic encephalopathy. By drawing water into the colon, it softens stools, and by converting ammonia to ammonium, it helps improve neurological symptoms associated with liver disease.

Lactulose is a synthetic sugar that reaches the colon unchanged, where gut bacteria break it down into short‑chain fatty acids. This creates an osmotic gradient that pulls water into the intestinal lumen, promoting bowel movements, and acidifies the colon, converting ammonia (NH3) to non‑absorbable ammonium (NH4+), thereby reducing systemic ammonia.

The dosage of Lactulose Biogaran is individualized by the prescribing clinician based on the patient’s condition, severity, and response. Healthcare professionals determine the appropriate volume and frequency to achieve the desired therapeutic effect while monitoring tolerance and clinical outcomes.

Safety data for Lactulose Biogaran 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 after evaluating the clinical situation.

To place an order, submit an enquiry on the Lactulose Biogaran 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, differing from stimulant laxatives that increase intestinal motility. Its dual action—softening stool and reducing ammonia absorption—makes it uniquely suited for patients with hepatic encephalopathy, whereas other laxatives lack the ammonia‑lowering effect.

Lactulose Biogaran should be stored at ambient temperature, preferably below 25 °C. Keep the container tightly closed, protect it from moisture and direct sunlight, and store it in its original packaging to maintain stability.

Lactulose Biogaran is taken orally as a liquid solution. The prescribed volume is measured with a calibrated dosing device and ingested directly or mixed with a small amount of water or juice, according to the healthcare provider’s instructions.

Serious risks include severe electrolyte imbalance, dehydration from excessive diarrhea, and rare allergic reactions such as rash or breathing difficulties. Patients should be monitored for signs of these conditions, especially during dose adjustments or in those with renal or cardiac disease.

Lactulose Biogaran is contraindicated in individuals with known hypersensitivity to lactulose or any component of the formulation. Caution is advised for patients with severe renal impairment, uncontrolled diabetes, or those at risk of electrolyte disturbances, and it should be avoided in such cases unless directed by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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