Product image of Levolac (Lactulose) supplied by GNH India

Levolac

Active Ingredient:
Lactulose
Origin:
EU

Levolac (Lactulose)

Lactulose, the active ingredient in Levolac, is an osmotic laxative presented as an oral preparation for oral use. It is employed to relieve constipation and to treat hepatic encephalopathy by lowering blood ammonia levels in adult patients.

GNH India supplies Levolac as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides regulatory documentation for export to multiple regions. Levolac is manufactured under GMP conditions and undergoes comprehensive testing to ensure batch consistency and safety.

Manufacturer / TM Owner

Orion Corporation

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Indications & Clinical Uses

Levolac (lactulose) acts as an osmotic laxative and ammonia‑lowering agent in the gastrointestinal tract.

  • Constipation: softens stool and promotes bowel movements, relieving chronic constipation.
  • Hepatic encephalopathy: lowers intestinal ammonia production, helping improve mental status in patients with liver disease.
  • Prevention of hepatic encephalopathy recurrence: maintains low ammonia levels to reduce the risk of future episodes.

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 osmotic pressure and draw water into the lumen. The resulting acidification of colonic contents converts ammonia (NH₃) to ammonium (NH₄⁺), trapping it in the gut and decreasing systemic absorption. This process also promotes a favorable shift in gut microbiota that further supports ammonia reduction.

Side Effects

Lactulose may cause several adverse reactions, ranging from mild gastrointestinal discomfort to rare serious events.

Common Side Effects

  • Bloating: sensation of abdominal fullness.
  • Diarrhea: loose stools, especially at higher doses.
  • Nausea: feeling of sickness.

Serious or Rare Side Effects

  • Severe dehydration: excessive fluid loss requiring medical attention.
  • Electrolyte imbalance: abnormal potassium or sodium levels.
  • Allergic reaction: rash, itching, or swelling.

Precautions & Warnings

When prescribing lactulose, clinicians should consider several safety measures to minimize risks.

  • Dose adjustment in renal impairment: monitor for accumulation and adjust as needed.
  • Monitor electrolytes: especially potassium and sodium during prolonged therapy.
  • Caution in diabetic patients: lactulose contains carbohydrate that may affect blood glucose.
  • Avoid abrupt discontinuation: sudden stop can lead to rebound constipation.
  • Pregnancy safety unknown: use only if potential benefit justifies risk.
  • Store at room temperature: keep in original container, protect from moisture and heat.

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: additive effect can cause severe diarrhea and dehydration.
  • Insulin or oral hypoglycemics: carbohydrate content may require dose adjustment.

Moderate Interactions (Monitor Closely)

  • Diuretics: monitor electrolyte status due to potential additive fluid loss.
  • Mineral supplements (e.g., calcium, magnesium): may affect absorption of lactulose.
  • Probiotics: may modify gut flora and influence lactulose metabolism.

Frequently Asked Questions

Levolac contains lactulose, which is prescribed to relieve chronic constipation and to treat hepatic encephalopathy in adults. In constipation, it softens stool and promotes bowel movements, while in hepatic encephalopathy it lowers intestinal ammonia levels, helping improve neurological symptoms.

Lactulose is a synthetic sugar that reaches the colon unchanged. Gut bacteria break it down into short‑chain fatty acids, increasing osmotic pressure and drawing water into the bowel. The resulting acidic environment converts ammonia to ammonium, trapping it in the gut and reducing its absorption into the bloodstream.

The dose of Levolac is individualized by the prescribing clinician based on the patient’s condition, severity, and response. No standard dosing can be provided here; the prescriber determines the appropriate amount and frequency for each patient.

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

To request Levolac, 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.

Levolac (lactulose) is an osmotic laxative that works by increasing water content in the colon, unlike stimulant laxatives that trigger intestinal muscle contractions. It is generally gentler and can be used for long‑term management, whereas stimulant agents may cause dependence or cramping with prolonged use.

Levolac should be stored at room temperature, below 25 °C, in its original packaging. Keep it away from moisture, direct sunlight and excessive heat to maintain product stability and potency.

Levolac is taken orally, usually as a liquid or solution. It is swallowed with water or another suitable fluid. The exact administration instructions, including timing relative to meals, are provided by the prescribing healthcare professional.

Serious risks include severe dehydration, electrolyte disturbances such as low potassium or sodium, and rare allergic reactions that may present as rash, itching or swelling. Patients should seek medical attention promptly if they experience these symptoms.

Levolac is contraindicated in patients with known hypersensitivity to lactulose. Caution is advised for individuals with severe renal impairment, uncontrolled diabetes, or those who are pregnant or breastfeeding unless the benefits outweigh the risks.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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