Lactulose 1 A Pharma (Lactulose)

Lactulose is a synthetic sugar that reaches the colon unchanged, where intestinal bacteria ferment it into short‑chain fatty acids. These acids increase the osmotic pressure inside the bowel, drawing water into the lumen and softening the stool. The resulting acidic environment also converts ammonia to ammonium, which is poorly absorbed, thus reducing systemic ammonia levels.

The dose of lactulose is individualized. A qualified prescriber determines the amount, frequency, and duration based on the specific condition being treated, the patient’s response, and any relevant clinical factors. Patients should follow the prescribing information provided by their healthcare professional.

Data on lactulose use during pregnancy and lactation are limited. It should only be used when the potential benefit justifies any possible risk to the fetus or infant. Healthcare providers will assess the individual situation and decide whether lactulose is appropriate for a pregnant or nursing patient.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies, and procurement teams worldwide. After the request, the sales team will verify trade or institutional credentials, then provide pricing, availability, shipping details (including any cold‑chain requirements if applicable), and the necessary import documentation.

Lactulose belongs to the osmotic laxative class, acting by increasing water content in the colon. Compared with stimulant laxatives (e.g., senna) it generally produces softer stools with less cramping. Polyethylene glycol (PEG) is another osmotic agent; lactulose also offers the added benefit of reducing ammonia absorption, making it useful for hepatic encephalopathy, a property PEG does not provide.

Lactulose should be stored at room temperature, below 25 °C, in its original container. Keep the product away from moisture, direct sunlight, and excessive heat. Ensure the seal remains intact until use, and keep it out of reach of children.

Lactulose is taken orally, usually dissolved in a glass of water or another suitable liquid. It may be consumed with or without food, as directed by the prescribing clinician. Patients should drink an adequate amount of fluid throughout the day to help prevent dehydration.

The most serious risks include severe dehydration, electrolyte disturbances such as low potassium or sodium, and rare allergic reactions that may present as rash, itching, swelling, or difficulty breathing. If any of these symptoms occur, medical attention should be sought promptly.

Lactulose should be avoided in individuals with known hypersensitivity to the product, those with intestinal obstruction, severe renal impairment, or active gastrointestinal bleeding. Patients with these conditions should consult their healthcare provider for alternative therapies.