Product image of Laxiriva Med Appelsin/Sitrussmak (Sodium Hydrogen Carbonate, Potassium Chloride, Sodium Chloride, Macrogol 3350) supplied by GNH India

Laxiriva Med Appelsin/Sitrussmak

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

Laxiriva Med Appelsin/Sitrussmak (Sodium Hydrogen Carbonate, Potassium Chloride, Sodium Chloride, Macrogol 3350)

Sodium hydrogen carbonate, potassium chloride, sodium chloride and macrogol 3350, the active ingredients in Laxiriva Med Appelsin/Sitrussmak, are an osmotic laxative presented as an oral solution for oral use. It is indicated for the relief of constipation in adults and children when a gentle, water‑based bowel‑cleansing action is required.

GNH India supplies Laxiriva Med Appelsin/Sitrussmak as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable global distribution, ensuring product integrity throughout the supply chain.

Manufacturer / TM Owner

Sandoz A/S

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Indications & Clinical Uses

  • Laxiriva Med is an osmotic laxative used to manage conditions characterized by difficult stool passage.
  • Constipation: softens stool and promotes regular bowel movements.
  • Chronic constipation: provides sustained hydration of the intestinal lumen to aid long‑term relief.
  • Functional constipation: improves stool frequency and reduces straining during defecation.

How It Works

  • Macrogol 3350 acts as an osmotic agent that retains water within the intestinal lumen, increasing stool volume and softness. The accompanying electrolytes—sodium hydrogen carbonate, potassium chloride and sodium chloride—help maintain fluid and electrolyte balance, supporting the laxative effect while minimizing the risk of electrolyte disturbance. This combined action facilitates gentle, effective bowel movements without stimulating intestinal muscles.

Side Effects

Laxiriva Med may be associated with several adverse reactions, most of which are mild and transient.

Common Side Effects

  • Abdominal bloating: mild distension of the abdomen.
  • Flatulence: increased intestinal gas.
  • Nausea: feeling of queasiness.
  • Diarrhea: loose, watery stools.

Serious or Rare Side Effects

  • Severe electrolyte imbalance: abnormal sodium, potassium or chloride levels.
  • Allergic reaction: rash, itching, swelling, or difficulty breathing.

Precautions & Warnings

  • Before initiating therapy, consider the following precautions to ensure safe use.
  • Assess renal function: ensure adequate kidney function before use.
  • Monitor fluid intake: maintain sufficient hydration to support osmotic activity.
  • Use with caution in electrolyte disorders: patients with hypernatremia or hypokalemia need evaluation.
  • Avoid prolonged use: limit duration to prevent dependence or electrolyte shifts.
  • Store at ambient temperature: keep below 25 °C, retain in original container, protect from moisture.

Avoid Interactions

Laxiriva Med can interact with other medicines; awareness of potential interactions helps maintain safety.

Major Interactions (Avoid)

  • Concomitant use with other osmotic laxatives: may cause excessive fluid loss and electrolyte imbalance.
  • High-dose mineral supplements (e.g., potassium chloride): can exacerbate electrolyte disturbances.

Moderate Interactions (Monitor Closely)

  • Antacids containing sodium bicarbonate: may alter electrolyte composition.
  • Diuretics: monitor for additive fluid loss.
  • Certain antibiotics (e.g., quinolones): reduced absorption due to altered gastrointestinal transit.

Frequently Asked Questions

Laxiriva Med is an oral osmotic laxative indicated for the relief of occasional or chronic constipation in adults and children. It works by increasing water content in the intestinal lumen, which softens stool and promotes regular bowel movements.

Macrogol 3350 is a high‑molecular‑weight polymer that retains water in the gut through osmotic pressure. This added water softens the stool, expands its volume, and stimulates peristalsis, facilitating easier passage without directly stimulating intestinal muscles.

The dose of Laxiriva Med is individualized by the prescribing healthcare professional based on the patient’s age, weight, severity of constipation, and response to therapy. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data for Laxiriva Med in pregnancy and lactation are limited. It should only be used if the potential benefit outweighs any possible risk to the fetus or infant, and under the guidance of a qualified healthcare provider.

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, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Compared with stimulant laxatives, Laxiriva Med provides a gentler, water‑based mechanism that is less likely to cause cramping. Unlike bulk‑forming agents, it does not rely on dietary fiber and works quickly by osmotic action, making it suitable for patients needing rapid relief.

Store Laxiriva Med at ambient temperature, preferably below 25 °C. Keep the bottle tightly closed in its original packaging, protect it from moisture and direct sunlight, and discard any product that shows signs of contamination or degradation.

Laxiriva Med is taken orally as a measured dose of the flavored solution. It should be consumed with a glass of water, and the patient should remain well‑hydrated throughout treatment to support its osmotic action.

The most serious risks include severe electrolyte disturbances such as hyponatremia or hyperkalemia, and rare allergic reactions that may present as rash, swelling, or difficulty breathing. Prompt medical attention is required if any of these symptoms occur.

Laxiriva Med should be avoided in individuals with known hypersensitivity to any of its ingredients, in patients with intestinal obstruction, perforation, or severe inflammatory bowel disease, and in those with uncontrolled electrolyte imbalances unless supervised by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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