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

Lactulose Al

Active Ingredient:
Lactulose
Origin:
EU

Lactulose Al (Lactulose)

Lactulose, the active ingredient in Lactulose Al, is an osmotic laxative presented as an oral formulation for oral use. It treats constipation and hepatic encephalopathy in adult patients.
GNH India supplies Lactulose Al as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Stada Arzneimittel Ag

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Indications & Clinical Uses

Lactulose acts on the gastrointestinal tract to relieve bowel stasis and lower ammonia absorption in liver disease.

  • Constipation: softens stool and increases bowel movement frequency.
  • Hepatic encephalopathy: reduces intestinal ammonia production, improving mental status.
  • Prevention of hepatic encephalopathy recurrence: maintains low ammonia levels to avoid relapse.

How It Works

  • Lactulose is a disaccharide that is not absorbed in the small intestine. In the colon it is metabolized by bacteria into short‑chain fatty acids, which increase the osmotic pressure within the lumen, drawing water into the bowel and promoting laxation while also trapping ammonia as ammonium ions, thereby reducing its systemic absorption.

Side Effects

Lactulose may cause several adverse reactions, ranging from mild to serious.

Common Side Effects

  • Flatulence: increased gas production in the colon.
  • Abdominal cramps: discomfort due to increased intestinal activity.
  • Diarrhea: loose stools from excess water in the lumen.
  • Nausea: mild upset stomach.
  • Bloating: sensation of fullness.
  • Thirst: increased fluid loss.

Serious or Rare Side Effects

  • Electrolyte imbalance: especially low potassium from prolonged diarrhea.
  • Severe dehydration: excessive fluid loss requiring medical attention.
  • Allergic reaction: rash, itching, or swelling.
  • Rectal bleeding: uncommon but warrants immediate evaluation.

Precautions & Warnings

Before prescribing lactulose, consider the following safety measures.

  • Renal function assessment: monitor kidney status as dehydration can worsen renal impairment.
  • Electrolyte monitoring: check serum potassium and sodium during long‑term use.
  • Diabetes caution: lactulose contains carbohydrate that may affect blood glucose.
  • Intestinal obstruction avoidance: do not use in patients with known bowel blockage.
  • Hepatic impairment dose adjustment: reduce dose if severe liver dysfunction is present.
  • Store at ambient temperature: keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

Lactulose can interact with other medicines, altering its efficacy or safety.

Major Interactions (Avoid)

  • Antidiarrheal agents (e.g., loperamide): may counteract lactulose’s laxative effect.
  • Antibiotics (e.g., rifaximin): can reduce bacterial metabolism of lactulose, diminishing ammonia‑lowering action.

Moderate Interactions (Monitor Closely)

  • Mineral supplements (calcium, magnesium): may bind lactulose and decrease its activity.
  • Oral hypoglycemic agents: carbohydrate content of lactulose may affect glucose control.
  • Proton‑pump inhibitors: may alter gut flora, potentially influencing lactulose metabolism.

Frequently Asked Questions

Lactulose Al is prescribed to relieve constipation and to treat or prevent hepatic encephalopathy, a brain disorder caused by high ammonia levels in patients with liver disease. It works by drawing water into the colon and reducing ammonia absorption.

Lactulose is a synthetic sugar that reaches the colon unchanged. Gut bacteria ferment it into short‑chain fatty acids, which increase the osmotic pressure in the intestinal lumen, pulling water into the bowel to soften stool. The acidic environment also converts ammonia to ammonium, limiting its absorption into the bloodstream.

The dose of Lactulose Al is individualized by the prescribing clinician based on the patient’s condition, severity, and response. Dosage may be adjusted to achieve the desired stool consistency or ammonia reduction, and should follow the healthcare professional’s instructions.

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 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, differing from stimulant laxatives that increase intestinal motility. It also has the unique ability to lower blood ammonia, making it useful for hepatic encephalopathy, a benefit not shared by most other laxatives.

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

Lactulose Al 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, as directed by the prescriber.

Serious risks include severe dehydration, electrolyte disturbances such as low potassium, and rare allergic reactions. Patients should seek medical attention if they experience persistent diarrhea, dizziness, muscle weakness, or signs of an allergic response.

Lactulose Al is contraindicated in individuals with known intestinal obstruction, severe bowel perforation, or hypersensitivity to lactulose. It should also be used with caution in patients with renal impairment or uncontrolled diabetes.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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