Product image of Lattulac Eps (Lactulose) supplied by GNH India

Lattulac Eps

Active Ingredient:
Lactulose
Origin:
EU

Lattulac Eps (Lactulose)

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

Manufacturer / TM Owner

Alfasigma S.P.A.

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Indications & Clinical Uses

  • Lactulose is employed in the treatment of gastrointestinal and hepatic disorders where reduction of intestinal ammonia and promotion of bowel movements are therapeutic goals.
  • Constipation: relieves stool hardness, increases frequency of bowel movements and eases passage of feces.
  • Hepatic encephalopathy: lowers blood ammonia concentrations, helping to improve mental status and prevent neurological deterioration.

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 to short‑chain fatty acids, which increase the osmotic pressure within the lumen, drawing water into the bowel and acidifying colonic contents. The resulting environment traps ammonia as ammonium ions, reducing its absorption into the portal circulation and thereby lowering systemic ammonia levels.

Side Effects

Lactulose may cause a range of adverse reactions, most of which are related to its laxative action.

Common Side Effects

  • Abdominal cramping or pain
  • Flatulence and bloating
  • Diarrhoea or loose stools
  • Nausea or mild vomiting
  • Increased thirst
  • Transient electrolyte imbalance (e.g., mild hyponatraemia)

Serious or Rare Side Effects

  • Severe dehydration requiring medical attention
  • Marked electrolyte disturbances (e.g., severe hyponatraemia, hypokalaemia)
  • Allergic reactions such as rash, itching or angioedema
  • Hepatic decompensation in patients with advanced liver disease

Precautions & Warnings

  • When using Lattulac Eps, clinicians should consider several safety measures to minimise risk.
  • Assess renal function: adjust use in patients with impaired kidney clearance.
  • Monitor electrolyte levels: watch for sodium and potassium changes during therapy.
  • Use caution in diabetes: lactulose may affect blood glucose control.
  • Avoid in intestinal obstruction: risk of perforation or worsening blockage.
  • Adjust dose in severe hepatic impairment: monitor ammonia and clinical response.
  • Store at room temperature: keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

Lactulose can interact with other medicines, altering its efficacy or increasing adverse effects.

Major Interactions (Avoid)

  • Antidiarrhoeal agents (e.g., loperamide): may counteract lactulose's laxative action.
  • Mineral oil: can reduce lactulose's effectiveness by coating the intestinal mucosa.
  • Certain antibiotics (e.g., broad‑spectrum): may disrupt colonic flora needed for lactulose metabolism.

Moderate Interactions (Monitor Closely)

  • Insulin or oral hypoglycaemic drugs: lactulose may enhance hypoglycaemia; monitor blood glucose.
  • Other laxatives or osmotic agents: additive effect may cause excessive fluid loss.
  • Phosphate binders: may interfere with lactulose’s ability to acidify colonic contents.

Frequently Asked Questions

Lattulac Eps contains lactulose and is indicated for the relief of constipation and for the management of hepatic encephalopathy, a condition caused by elevated ammonia levels in patients with liver disease.

Lactulose is metabolised by colonic bacteria into acidic compounds that increase osmotic pressure, drawing water into the intestine and softening stool. The acidified environment also converts ammonia to ammonium, which is less readily absorbed, thereby lowering systemic ammonia levels.

The appropriate dose of Lattulac Eps is determined by the prescribing clinician based on the patient’s condition, severity, and response to therapy. Dosage may be adjusted during treatment to achieve the desired clinical effect.

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

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 drawing water into the colon, unlike stimulant laxatives that increase intestinal motility. It also has the unique ability to lower ammonia levels, a benefit not shared by most other laxatives, making it the preferred choice for patients with hepatic encephalopathy.

Store Lattulac Eps at room temperature, preferably below 25 °C. Keep the container tightly closed, protect it from moisture and direct sunlight, and store it in its original packaging until use.

Lattulac Eps is a rectal solution that is administered via the rectum, typically using a calibrated enema device. The exact administration technique and volume are determined by the prescribing clinician.

Serious risks include severe dehydration, marked electrolyte disturbances such as hyponatraemia or hypokalaemia, and rare allergic reactions. Patients should be monitored for signs of these conditions, especially during high‑dose or prolonged therapy.

Lattulac Eps should be avoided in patients with known hypersensitivity to lactulose, in those with complete intestinal obstruction, and in individuals where the risk of severe dehydration or electrolyte imbalance outweighs the therapeutic benefit.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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