Product image of Movicol Med Sjokoladesmak (Sodium Hydrogen Carbonate, Potassium Chloride, Sodium Chloride, Macrogol 3350) supplied by GNH India

Movicol Med Sjokoladesmak

Active Ingredient:
Sodium Hydrogen Carbonate, Potassium Chloride, Sodium Chloride, Macrogol 3350
Origin:
EU

Movicol Med Sjokoladesmak (Sodium Hydrogen Carbonate, Potassium Chloride, Sodium Chloride, Macrogol 3350)

Macrogol 3350 with electrolytes, the active ingredient in Movicol Med Sjokoladesmak, is an osmotic laxative presented as an oral powder for oral administration. It creates an osmotic gradient that retains water in the intestinal lumen, softening stool and facilitating regular bowel movements, and is used to relieve constipation in both adult and paediatric patients.

GNH India supplies Movicol Med Sjokoladesmak as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, providing reliable sourcing and regulatory‑aligned distribution for this essential constipation therapy.

Manufacturer / TM Owner

Norgine Healthcare B.V.

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Indications & Clinical Uses

Movicol Med Sjokoladesmak, an osmotic laxative, is used to manage conditions characterized by difficult stool passage.

  • Constipation: softens stool and increases bowel frequency to relieve occasional or chronic constipation.
  • Chronic idiopathic constipation: provides sustained stool softening for long‑term management.
  • Opioid‑induced constipation: counteracts reduced gastrointestinal motility caused by opioid therapy.

How It Works

  • Macrogol 3350 with electrolytes acts as a high‑molecular‑weight polymer that is poorly absorbed in the gastrointestinal tract. It binds water molecules, creating an osmotic gradient that retains water within the intestinal lumen. The added electrolytes (sodium, potassium, chloride) maintain fluid balance, while the increased intraluminal water softens feces and expands stool volume, stimulating peristalsis and facilitating bowel evacuation.

Side Effects

Common and serious adverse reactions have been reported with osmotic laxatives such as Movicol Med Sjokoladesmak.

Common Side Effects

  • Abdominal bloating: sensation of fullness in the abdomen.
  • Nausea: mild to moderate feeling of sickness.
  • Flatulence: increased intestinal gas.
  • Diarrhoea: loose stools occurring more frequently.

Serious or Rare Side Effects

  • Electrolyte imbalance: abnormal sodium or potassium levels.
  • Severe dehydration: marked loss of body fluids.
  • Allergic reaction: rash, itching or swelling.
  • Severe abdominal pain: intense, persistent pain.

Precautions & Warnings

When prescribing Movicol Med Sjokoladesmak, consider the following precautions to ensure safe use.

  • Renal function assessment: evaluate kidney function before initiating therapy.
  • Electrolyte monitoring: check serum electrolytes periodically, especially in high‑risk patients.
  • Bowel obstruction: avoid use in patients with known or suspected intestinal blockage.
  • Elderly dosing: start with the lowest effective dose in older adults.
  • Concomitant diuretics: use caution as combined effect may alter fluid balance.
  • Store at ambient temperature: keep in original packaging, protect from moisture and excessive heat.

Avoid Interactions

Movicol Med Sjokoladesmak may interact with other medicines; awareness of these interactions helps prevent complications.

Major Interactions (Avoid)

  • Other osmotic laxatives: concurrent use can cause severe diarrhoea and electrolyte loss.
  • High‑dose potassium supplements: may lead to hyperkalaemia when combined with the product’s potassium content.
  • Loop diuretics: increased risk of electrolyte disturbances and dehydration.

Moderate Interactions (Monitor Closely)

  • Antacids containing sodium or potassium: may affect electrolyte balance and require monitoring.
  • ACE inhibitors or ARBs: combined use can increase the chance of hyperkalaemia.

Frequently Asked Questions

Movicol Med Sjokoladesmak is indicated for the treatment of constipation. It helps soften stool and increase bowel movement frequency, providing relief for occasional, chronic, or opioid‑induced constipation in adult and paediatric patients.

Macrogol 3350 is a high‑molecular‑weight polymer that is not absorbed in the gut. It attracts and holds water in the intestinal lumen, creating an osmotic gradient that softens stool and expands its volume, which stimulates peristalsis and promotes easier evacuation.

The appropriate dose of Movicol Med Sjokoladesmak is determined by the prescribing healthcare professional based on the patient’s age, severity of constipation, and individual response. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data for Macrogol‑based laxatives during pregnancy and lactation are limited. Healthcare providers should weigh the potential benefits against any possible risks and consider alternative treatments if appropriate. Pregnant or nursing women should consult their doctor before using this product.

To order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, and will request verification of trade or institutional credentials. The sales team then provides pricing, availability, shipping details and any necessary import documentation.

Compared with stimulant laxatives, Movicol Med Sjokoladesmak works by osmotic water retention rather than stimulating intestinal muscle contractions. This generally results in a gentler, more physiologic stool softening with a lower risk of cramping, making it suitable for long‑term use in many patients.

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

Movicol Med Sjokoladesmak is supplied as an oral powder that should be dissolved in a specified amount of water, as indicated on the label. The solution is then consumed orally, usually once or twice daily, according to the prescriber’s directions.

Serious risks include electrolyte imbalance (especially sodium or potassium disturbances), severe dehydration, and rare allergic reactions such as rash or swelling. Patients should seek medical attention if they experience symptoms like persistent vomiting, severe abdominal pain, or signs of an allergic response.

The product should be avoided in individuals with known or suspected intestinal obstruction, severe renal impairment, or a documented hypersensitivity to any of its ingredients. It is also contraindicated in patients with significant electrolyte disorders unless closely monitored by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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