Lactulosestroop Albert Heijn (Lactulose)

Lactulose is a synthetic sugar that reaches the colon unchanged, where intestinal bacteria break it down into short‑chain acids. These acids raise the osmotic pressure, drawing water into the bowel to stimulate peristalsis, and they acidify the lumen, converting ammonia to ammonium, which is less readily absorbed, thereby reducing systemic ammonia levels.

The appropriate dose of lactulose is individualized by the prescribing clinician based on the patient’s condition, severity, and response. Dosage may be adjusted to achieve the desired stool consistency or ammonia reduction, and patients should follow the prescriber’s instructions without self‑adjusting the amount.

Safety data for lactulose in pregnancy and lactation are limited. It is generally categorized as a drug that should be used only if the potential benefit justifies any potential risk to the fetus or infant. Healthcare providers should evaluate the risk‑benefit profile for each patient.

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 (including any cold‑chain requirements) and assistance with import documentation.

Lactulose is an osmotic laxative, whereas stimulant laxatives (e.g., bisacodyl) act by directly stimulating intestinal nerves. Osmotic agents like lactulose are often preferred for chronic constipation and for hepatic encephalopathy because they also lower colonic ammonia. Stimulants may cause cramping and are generally used for short‑term relief.

Store the product at ambient temperature, preferably below 25 °C, in its original container. Protect it from moisture, direct sunlight, and extreme temperature fluctuations. Ensure the bottle is tightly closed after each use to maintain product stability.

Lactulosestroop Albert Heijn is taken orally as a liquid. The prescribed amount is measured with a calibrated dosing device (spoon or cup) and ingested directly or mixed with a small amount of water or juice. Dosing frequency is determined by the prescriber.

Serious risks include severe electrolyte imbalance (especially low potassium), dehydration from excessive diarrhea, and allergic reactions such as rash, itching, or swelling. Patients experiencing these symptoms should seek medical attention promptly.

Lactulose is contraindicated in individuals with known hypersensitivity to lactulose, in patients with complete intestinal obstruction, and in those with severe dehydration until fluid balance is restored. Caution is also advised for patients with renal impairment or uncontrolled diabetes.