Product image of Izetafin (Sodium Hydrogen Carbonate, Potassium Chloride, Sodium Chloride, Sodium Sulfate Anhydrous, Macrogol 3) supplied by GNH India

Izetafin

Active Ingredient:
Sodium Hydrogen Carbonate, Potassium Chloride, Sodium Chloride, Sodium Sulfate Anhydrous, Macrogol 3
Origin:
EU

Izetafin (Sodium Hydrogen Carbonate, Potassium Chloride, Sodium Chloride, Sodium Sulfate Anhydrous, Macrogol 3)

Sodium hydrogen carbonate, potassium chloride, sodium chloride, sodium sulfate anhydrous and macrogol 3, the active ingredients in Izetafin, are presented as an oral solution for oral use. They are employed to correct electrolyte disturbances and to provide an osmotic laxative effect in adult patients.

GNH India supplies Izetafin as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Rafarm Sa.

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Indications & Clinical Uses

Izetafin is a combined electrolyte and osmotic laxative formulation used in clinical settings for fluid and electrolyte management and bowel preparation.

  • Electrolyte imbalance: restores sodium, potassium and chloride levels in patients with dehydration.
  • Constipation: provides an osmotic laxative effect to facilitate bowel movements.
  • Diagnostic procedure preparation: used as a bowel cleansing agent before colonoscopy or imaging studies.

How It Works

  • Izetafin supplies essential electrolytes (sodium, potassium, chloride, sulfate) that are absorbed in the gastrointestinal tract to replenish fluid balance, while macrogol 3 (polyethylene glycol) acts as an osmotic agent that retains water in the intestinal lumen, softening stool and promoting evacuation without significant systemic absorption.

Side Effects

Izetafin may be associated with a range of adverse reactions, most of which are mild and transient.

Common Side Effects

  • Nausea: mild discomfort in the stomach.
  • Abdominal bloating: feeling of fullness or swelling.
  • Diarrhea: loose stools occurring after dosing.
  • Flatulence: increased intestinal gas.
  • Electrolyte disturbance: occasional mild shifts in serum levels.
  • Headache: transient mild pain.

Serious or Rare Side Effects

  • Severe dehydration: marked loss of fluids requiring medical attention.
  • Electrolyte imbalance: significant hypo‑ or hyper‑natremia or hyper‑kalemia.
  • Allergic reaction: rash, itching, or swelling.
  • Abdominal pain: persistent or severe discomfort.
  • Renal impairment: worsening kidney function in susceptible individuals.
  • Hypotension: low blood pressure due to fluid shifts.

Precautions & Warnings

Before using Izetafin, consider the following safety measures.

  • Assess hydration status: ensure patient is not severely dehydrated before administration.
  • Monitor electrolytes: check serum sodium, potassium and chloride levels during therapy.
  • Renal function: evaluate kidney function in patients with existing renal disease.
  • Pregnancy and lactation: use only if clearly needed and prescribed by a healthcare professional.
  • Concomitant laxatives: avoid simultaneous use of other osmotic agents to prevent excessive fluid loss.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Izetafin may interact with other medicines; awareness of potential interactions helps maintain safety.

Major Interactions (Avoid)

  • Loop diuretics: may exacerbate electrolyte loss and dehydration.
  • Potassium‑sparing agents: risk of hyper‑kalemia when combined.
  • Antihypertensives: possible additive blood pressure lowering effect.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs: monitor renal function and electrolytes.
  • NSAIDs: may affect renal perfusion when combined with electrolyte shifts.
  • Other oral laxatives: increase risk of severe diarrhea and electrolyte disturbances.

Frequently Asked Questions

Izetafin is an oral solution that combines electrolytes and an osmotic laxative. It is used to correct fluid and electrolyte imbalances and to prepare the bowel for diagnostic procedures such as colonoscopy.

The formulation supplies sodium, potassium, chloride and sulfate ions that are absorbed to restore electrolyte balance, while macrogol 3 (polyethylene glycol) retains water in the intestinal lumen, creating an osmotic effect that softens stool and promotes evacuation.

The dose of Izetafin is determined by the prescribing healthcare professional based on the patient’s clinical condition, age, weight and the specific indication. Patients should follow the prescriber’s instructions exactly.

Izetafin should be used in pregnancy or while breastfeeding only if the potential benefit justifies any potential risk to the fetus or infant. The decision must be made by a qualified healthcare provider.

To order Izetafin, submit an enquiry on the product page at gnhindia.com with 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.

Izetafin combines multiple electrolytes with macrogol 3, offering both electrolyte repletion and an osmotic laxative effect in a single product. Compared with simple saline solutions, it provides a broader electrolyte profile and added bowel‑cleansing capability.

Izetafin should be stored at ambient temperature, below 25 °C, in its original container. Keep the product away from moisture, direct sunlight and extreme heat to maintain stability.

Izetafin is taken orally as a liquid solution. The prescribed volume is measured using a calibrated device and ingested according to the healthcare professional’s directions, usually with or without food as indicated.

Serious risks include severe dehydration, significant electrolyte disturbances such as hyper‑kalemia or hyponatremia, and allergic reactions. Patients should be monitored for signs of these conditions, especially if they have renal impairment or are on interacting medications.

Izetafin should be avoided in patients with known hypersensitivity to any of its components, in those with severe renal failure, uncontrolled electrolyte disorders, or in individuals taking medications that could cause dangerous electrolyte shifts without close monitoring.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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