Product image of Lactulose Greenwood (Lactulose) supplied by GNH India

Lactulose Greenwood

Active Ingredient:
Lactulose
Origin:
EU

Lactulose Greenwood (Lactulose)

Lactulose, the active ingredient in Lactulose Greenwood, is an osmotic laxative presented as an oral formulation for oral use. It is employed to relieve constipation and to lower blood ammonia levels in patients with hepatic encephalopathy, helping to improve bowel movements and mental status in liver disease.
GNH India supplies Lactulose Greenwood as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Relax Ltd.

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Indications & Clinical Uses

Lactulose acts as an osmotic laxative and ammonia‑lowering agent in the gastrointestinal tract.

  • Constipation: softens stool and promotes regular bowel movements.
  • Hepatic encephalopathy: reduces intestinal ammonia absorption, improving neurological function in liver disease.
  • Prevention of constipation in patients with chronic liver disease: helps maintain bowel regularity to support ammonia control.

How It Works

  • Lactulose is a synthetic disaccharide that is not absorbed in the small intestine. In the colon it is metabolized by bacterial flora into short‑chain fatty acids, which increase osmotic pressure and draw water into the lumen, softening stool. The resulting acidification of colonic contents converts ammonia to ammonium, decreasing its absorption and lowering systemic ammonia levels.

Side Effects

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

Common Side Effects

  • Flatulence: increased gas production in the colon.
  • Diarrhea: loose stools due to osmotic effect.
  • Abdominal cramping: discomfort from increased intestinal activity.
  • Nausea: mild stomach upset.
  • Bloating: sensation of fullness.

Serious or Rare Side Effects

  • Severe dehydration: excessive fluid loss from prolonged diarrhea.
  • Electrolyte imbalance: abnormal potassium or sodium levels.
  • Hypernatremia: elevated blood sodium from fluid shifts.
  • Allergic reaction: rash, itching, or swelling.
  • Hepatic encephalopathy worsening: paradoxical increase in ammonia in rare cases.

Precautions & Warnings

Before using Lactulose, consider the following safety measures.

  • Renal impairment: monitor fluid and electrolyte status closely.
  • Diabetes mellitus: assess blood glucose as lactulose may affect sugar levels.
  • Pediatric use: adjust dosing carefully under medical supervision.
  • Pregnancy: use only if clearly needed after risk‑benefit evaluation.
  • Lactose intolerance: consider alternative laxatives if intolerance is severe.
  • 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 medicines, affecting their absorption or efficacy.

Major Interactions (Avoid)

  • Antacids containing magnesium or aluminum: may reduce lactulose effectiveness.
  • Antibiotics (e.g., rifaximin): can alter gut flora, potentially diminishing lactulose’s ammonia‑lowering action.

Moderate Interactions (Monitor Closely)

  • Diabetic medications: monitor blood glucose as lactulose may affect glycemic control.
  • Diuretics: watch for signs of dehydration and electrolyte disturbances.
  • Other laxatives: combined use may cause severe diarrhea and electrolyte loss.

Frequently Asked Questions

Lactulose Greenwood is used to treat constipation by softening stools and to manage hepatic encephalopathy by lowering intestinal ammonia absorption, helping improve mental function in patients with liver disease.

Lactulose reaches the colon unchanged, where gut bacteria ferment it into short‑chain fatty acids. This creates an osmotic gradient that draws water into the bowel, softening stool, and acidifies the colon, converting ammonia to non‑absorbable ammonium, thereby reducing blood ammonia levels.

The dose of Lactulose Greenwood is individualized; the prescribing clinician determines the amount and frequency based on the patient’s condition, response, and tolerance.

Lactulose should be used in pregnancy or while breastfeeding only if the potential benefit justifies any possible risk to the fetus or infant. Decisions are made by the healthcare provider after evaluating the clinical situation.

To 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.

Unlike stimulant laxatives, lactulose works osmotically, drawing water into the colon without stimulating intestinal muscles. It also has the unique ability to lower ammonia levels, a property not shared by most other laxatives, making it valuable for hepatic encephalopathy.

Lactulose Greenwood should be stored at ambient temperature, below 25 °C, in its original packaging. Keep it away from moisture and direct sunlight to maintain product stability.

Lactulose Greenwood is taken orally, usually as a liquid or syrup. It can be measured with a calibrated dosing device and swallowed directly or mixed with a small amount of water or juice if needed.

Serious risks include severe dehydration, electrolyte imbalances such as hyponatremia or hypernatremia, and rare allergic reactions. Patients should seek medical attention if they experience persistent diarrhea, dizziness, or signs of an allergic response.

Lactulose is contraindicated in individuals with known hypersensitivity to lactulose or any component of the formulation, and should be used with caution in patients with severe renal impairment, uncontrolled diabetes, or those at risk of electrolyte disturbances.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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