Product image of Lattulosio Teva (Lactulose) supplied by GNH India

Lattulosio Teva

Active Ingredient:
Lactulose
Origin:
EU

Lattulosio Teva (Lactulose)

Lactulose, the active ingredient in Lattulosio, is an osmotic laxative presented as an oral solution for oral use. It is used to treat constipation and to prevent or treat hepatic encephalopathy in patients with liver disease.

GNH India supplies Lattulosio as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Teva Italia S.R.L.

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Indications & Clinical Uses

Lactulose acts as an osmotic agent to relieve bowel stasis and to lower blood ammonia levels in liver disease.

  • Constipation: softens stools and promotes bowel movements.
  • Hepatic encephalopathy: reduces ammonia absorption, helping to improve mental status.
  • Pediatric constipation: provides a safe, non‑stimulant option for children with functional constipation.

How It Works

  • Lactulose is metabolized by colonic bacteria into short‑chain fatty acids, primarily lactic and acetic acid. This creates an osmotic gradient that retains water in the intestinal lumen, increasing stool volume and promoting peristalsis. In the colon, the acidic environment traps ammonia as ammonium ions, reducing its absorption into the bloodstream 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

  • Abdominal cramping: discomfort due to increased intestinal activity.
  • Flatulence: excess gas production from bacterial fermentation.
  • Diarrhea: loose stools from osmotic water retention.
  • Nausea: mild stomach upset.
  • Bloating: sensation of fullness.
  • Thirst: increased fluid loss.

Serious or Rare Side Effects

  • Severe dehydration: excessive fluid loss requiring medical attention.
  • Electrolyte imbalance: particularly low potassium or sodium levels.
  • Allergic reaction: rash, itching, or swelling.
  • Hepatic decompensation: worsening liver function in susceptible patients.

Precautions & Warnings

When prescribing lactulose, clinicians should consider several safety aspects.

  • Assess renal function: impaired kidneys may affect drug clearance.
  • Monitor electrolytes: risk of hyponatremia or hypokalemia.
  • Use caution in diabetes: monitor blood glucose as lactulose can affect carbohydrate metabolism.
  • Avoid in intestinal obstruction: risk of perforation.
  • Store at ambient temperature: keep in the original container, protect from moisture.

Avoid Interactions

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

Major Interactions (Avoid)

  • Antibiotics (e.g., rifaximin): may reduce lactulose's ammonia‑lowering effect.
  • Other laxatives (e.g., senna): additive laxative action can cause severe diarrhea.

Moderate Interactions (Monitor Closely)

  • Antidiabetic agents: monitor glucose as lactulose may affect glycemic control.
  • Mineral supplements (e.g., calcium, magnesium): may interfere with absorption.
  • Diuretics: watch for electrolyte disturbances.
  • Oral hypoglycemics: adjust dose if needed.
  • Proton pump inhibitors: may alter gut flora and lactulose metabolism.

Frequently Asked Questions

Lattulosio contains lactulose, an osmotic laxative used to relieve constipation and to prevent or treat hepatic encephalopathy by lowering blood ammonia levels in patients with liver disease.

Lactulose is broken down by colonic bacteria into short‑chain fatty acids, creating an osmotic pull that retains water in the intestine, softening stools, and acidifying the colon to trap ammonia as ammonium, reducing its absorption.

The dose of lactulose is individualized by the prescribing clinician based on the patient’s condition, age, renal and hepatic function, and response to therapy. No fixed regimen is provided here.

Safety data are limited; lactulose is classified as pregnancy category unknown. It should be used only if the potential benefit justifies any potential risk to the fetus or infant, and the prescriber should evaluate each case.

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 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 polyethylene glycol formulations.

Store at ambient temperature, preferably below 25 °C. Keep the product in its original packaging, protect it from moisture and direct sunlight, and ensure the container is tightly closed to maintain stability.

Lattulosio is taken orally, usually as a liquid solution. The patient should follow the prescriber’s instructions regarding the volume and frequency, and may mix the dose with water or a suitable beverage if needed.

Serious risks include severe dehydration, electrolyte imbalances such as hyponatremia or hypokalemia, and rare allergic reactions. Patients should be monitored for signs of these conditions, especially if high doses are used.

Lactulose should be avoided in patients with known intestinal obstruction, severe renal impairment without monitoring, or hypersensitivity to lactulose or any excipients. Clinicians should assess each patient’s medical history before prescribing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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