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

Lactulose Arrow

Active Ingredient:
Lactulose
Origin:
EU

Lactulose Arrow (Lactulose)

Lactulose, the active ingredient in Lactulose Arrow, is an osmotic laxative presented as an oral formulation for oral use. It is used to relieve constipation and to reduce ammonia absorption in patients with hepatic encephalopathy.
GNH India supplies Lactulose Arrow as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Arrow Generiques

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Indications & Clinical Uses

  • Lactulose acts as an osmotic laxative and ammonia‑lowering agent in gastrointestinal and hepatic conditions.
  • Constipation: softens stools and promotes bowel movements.
  • Hepatic encephalopathy: lowers blood ammonia levels to improve neurological function.
  • Hyperammonemia in liver disease: helps reduce elevated ammonia concentrations.

How It Works

  • Lactulose is a synthetic disaccharide that is not absorbed in the small intestine. In the colon it is metabolized by bacteria into lactic acid and acetic acid, lowering colonic pH. The resulting acidification converts ammonia (NH3) to ammonium (NH4+), which is trapped and excreted. The increased osmotic load draws water into the lumen, softening stool and stimulating peristalsis.

Side Effects

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

Common Side Effects

  • Bloating: sensation of abdominal fullness.
  • Flatulence: increased intestinal gas.
  • Abdominal cramps: mild to moderate discomfort.
  • Diarrhea: loose stools, especially at higher doses.
  • Nausea: feeling of sickness.
  • Taste disturbance: sweet or fermented taste.

Serious or Rare Side Effects

  • Severe dehydration: excessive fluid loss requiring medical attention.
  • Electrolyte imbalance: abnormal sodium or potassium levels.
  • Allergic reaction: rash, itching, swelling, or difficulty breathing.
  • Severe abdominal pain: persistent or worsening pain.
  • Rectal bleeding: blood in stool indicating mucosal injury.

Precautions & Warnings

Before initiating Lactulose therapy, consider the following precautions.

  • Renal function assessment: evaluate kidney status to avoid accumulation.
  • Electrolyte monitoring: check sodium and potassium levels during treatment.
  • Diabetes caution: monitor blood glucose as lactulose contains carbohydrates.
  • Intestinal obstruction: avoid use in patients with known blockage.
  • Hepatic impairment: adjust dose based on liver function.
  • Store at ambient temperature: keep in the original pack, protect from moisture.

Avoid Interactions

Lactulose can interact with other medications, affecting its efficacy or safety.

Major Interactions (Avoid)

  • Antidiarrheal agents (e.g., loperamide): may reduce Lactulose's laxative effect.
  • High‑dose mineral supplements (e.g., magnesium): can increase osmotic load and cause severe diarrhea.
  • Oral antibiotics: may alter gut flora, affecting Lactulose metabolism.

Moderate Interactions (Monitor Closely)

  • Diabetic medications: monitor glucose as Lactulose may affect carbohydrate balance.
  • Proton pump inhibitors: may influence gastric pH and bacterial activity.
  • Other laxatives: combined use may lead to excessive fluid loss.

Frequently Asked Questions

Lactulose Arrow is used to relieve constipation and to lower blood ammonia levels in patients with hepatic encephalopathy, helping to improve bowel function and neurological symptoms associated with liver disease.

Lactulose reaches the colon unchanged, where bacterial enzymes convert it into acidic metabolites that lower colonic pH. This acidification traps ammonia as ammonium for excretion and creates an osmotic gradient that draws water into the intestine, softening stool and promoting evacuation.

The dose of Lactulose Arrow is individualized by the prescribing healthcare professional based on the patient’s condition, response, and tolerance. The prescriber determines the appropriate amount and frequency.

Safety of Lactulose Arrow in pregnancy or while nursing has not been definitively established. Healthcare providers should weigh potential benefits against possible risks before prescribing it to pregnant or lactating individuals.

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 necessary import documentation.

Lactulose is an osmotic laxative that works by increasing water content in the colon, whereas stimulant laxatives such as senna act by stimulating intestinal muscle contractions. Lactulose also has the unique benefit of reducing ammonia levels, a property not shared by most other laxatives.

Lactulose Arrow should be stored at ambient temperature, below 25 °C, in its original packaging to protect it from moisture and light. Keep the container tightly closed and out of reach of children.

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

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

Lactulose Arrow should be avoided in individuals with known intestinal obstruction, severe renal impairment, or hypersensitivity to lactulose. It should also be used with caution in patients with diabetes or those taking certain medications that may interact.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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