Product image of Isofundin (Magnesium Chloride Hexahydrate, Potassium Chloride, Sodium Chloride, Calcium Chloride Dihydrate, Sod) supplied by GNH India

Isofundin

Active Ingredient:
Magnesium Chloride Hexahydrate, Potassium Chloride, Sodium Chloride, Calcium Chloride Dihydrate, Sod
Origin:
EU

Isofundin (Magnesium Chloride Hexahydrate, Potassium Chloride, Sodium Chloride, Calcium Chloride Dihydrate, Sod)

Magnesium chloride hexahydrate, potassium chloride, sodium chloride and calcium chloride dihydrate, the active ingredients in Isofundin, are an electrolyte solution presented as an injectable solution for intravenous use. It provides electrolyte replacement and fluid resuscitation in patients requiring restoration of extracellular fluid volume and maintenance of electrolyte balance. It is indicated for use in surgical, trauma, and intensive care settings where rapid correction of electrolyte deficits is essential.

GNH India supplies Isofundin as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

B.Braun Melsungen Ag

1
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Indications & Clinical Uses

Isofundin is an intravenous electrolyte solution used to correct disturbances in fluid and electrolyte balance.

  • Electrolyte replacement: Restores magnesium, potassium, sodium and calcium levels in patients with documented deficits.
  • Fluid resuscitation: Provides isotonic fluid volume to support circulatory volume in hypovolemic states such as hemorrhage or severe dehydration.
  • Maintenance of electrolyte balance: Helps sustain normal electrolyte concentrations during prolonged fasting, surgery, or critical illness.
  • Post‑operative care: Supports electrolyte homeostasis after major surgery.
  • Burn injuries: Supplies necessary ions to counteract losses from extensive fluid shifts.

How It Works

  • Isofundin delivers magnesium, potassium, sodium and calcium ions directly into the bloodstream. The ions increase extracellular osmolarity, expanding plasma volume and correcting electrolyte deficits. Magnesium and calcium act as cofactors for enzymatic processes, while potassium and sodium are essential for cellular membrane potential and fluid balance. By replenishing these ions, the solution helps normalize nerve conduction, muscle contractility and cardiovascular function.

Side Effects

Isofundin may be associated with infusion‑related adverse reactions.

Common Side Effects

  • Injection site pain or erythema: mild discomfort at the catheter site.
  • Transient hypermagnesemia: temporary elevation of serum magnesium.
  • Nausea or vomiting: mild gastrointestinal upset.
  • Headache: mild to moderate headache during or after infusion.

Serious or Rare Side Effects

  • Severe hypermagnesemia: can cause hypotension, respiratory depression, or cardiac arrhythmia.
  • Severe hyperkalemia: may lead to life‑threatening cardiac arrhythmias.
  • Anaphylactic reaction: rare systemic allergic response.

Precautions & Warnings

When using Isofundin, clinicians should observe specific precautions to ensure patient safety.

  • Assess electrolyte levels: obtain baseline serum magnesium, potassium, sodium and calcium before infusion.
  • Adjust dose in renal impairment: reduce infusion rate or volume in patients with reduced renal clearance.
  • Monitor cardiac rhythm: continuous ECG monitoring is advised during rapid correction of potassium or magnesium.
  • Avoid in hyperkalemia: do not administer if serum potassium is already elevated beyond therapeutic range.
  • Use aseptic technique: ensure sterile handling to prevent contamination of the injectable solution.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Isofundin can interact with other medications that affect electrolyte balance or cardiac conduction.

Major Interactions (Avoid)

  • Calcium channel blockers: may potentiate hypercalcemia when combined with high calcium infusion.
  • Digoxin: increased risk of arrhythmia with concurrent hyperkalemia.
  • Loop diuretics: may cause rapid shifts in potassium and magnesium levels.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors or ARBs: monitor potassium levels to avoid hyperkalemia.
  • Beta‑adrenergic agonists: may influence serum potassium distribution.
  • Antacids containing magnesium or aluminum: assess cumulative magnesium load.

Frequently Asked Questions

Isofundin is an intravenous electrolyte solution indicated for electrolyte replacement, fluid resuscitation, and maintenance of electrolyte balance in patients who have lost fluids or electrolytes due to surgery, trauma, dehydration, or critical illness.

The formulation supplies magnesium, potassium, sodium and calcium ions directly into the bloodstream. These ions restore extracellular fluid volume, correct specific electrolyte deficits, and support cellular functions such as nerve conduction, muscle contraction and cardiac rhythm regulation.

The dose of Isofundin is determined by the prescribing clinician based on the patient’s electrolyte profile, fluid status, weight, and clinical condition. Dosage is individualized and administered under medical supervision.

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

To order Isofundin, 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 cold‑chain if required) and necessary import documentation.

Isofundin provides a balanced combination of magnesium, potassium, sodium and calcium, whereas many standard saline solutions contain only sodium and chloride. This broader ion profile can be advantageous in settings where multiple electrolyte deficits need simultaneous correction, reducing the need for additional supplemental infusions.

Isofundin should be stored at 2‑8 °C, protected from light, and must not be frozen or shaken. Keep the vial in its original packaging until use and inspect for particulate matter before administration.

Isofundin is administered intravenously. It is typically diluted in an appropriate carrier solution and infused over a period determined by the prescriber, with continuous monitoring of vital signs and electrolyte levels during the infusion.

Serious risks include severe hypermagnesemia, which can cause hypotension, respiratory depression, or cardiac arrhythmias; severe hyperkalemia, which may precipitate life‑threatening arrhythmias; and rare anaphylactic reactions. Prompt recognition and management of these events are essential.

Isofundin is contraindicated in patients with known hypersensitivity to any of its components, in those with severe hyperkalemia or hypermagnesemia, and in individuals where rapid electrolyte shifts could exacerbate existing cardiac conduction disorders.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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