Product image of Kalium-Natrium-Glucose Braun (Potassium Chloride, Sodium Chloride, Glucose Monohydrate) supplied by GNH India

Kalium-Natrium-Glucose Braun

Active Ingredient:
Potassium Chloride, Sodium Chloride, Glucose Monohydrate
Origin:
EU

Kalium-Natrium-Glucose Braun (Potassium Chloride, Sodium Chloride, Glucose Monohydrate)

Potassium chloride, sodium chloride and glucose monohydrate, the active ingredients in Kalium-Natrium-Glucose Braun, are an electrolyte solution presented as an injection solution for intravenous or subcutaneous use. It is used to replace electrolytes and provide metabolic energy in patients with electrolyte disturbances, dehydration or after surgery.

GNH India supplies Kalium-Natrium-Glucose Braun as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

B.Braun Melsungen Ag

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Indications & Clinical Uses

Kalium-Natrium-Glucose Braun is an electrolyte solution used in conditions that require restoration of potassium, sodium and glucose levels.

  • Electrolyte replacement: restores deficient potassium, sodium and glucose in patients with fluid loss.
  • Hypokalemia: raises low serum potassium concentrations.
  • Hyponatremia: corrects low serum sodium levels.
  • Dehydration: supplies essential electrolytes and energy during rehydration.
  • Post‑operative fluid therapy: maintains electrolyte balance after surgery.

How It Works

  • The injection delivers potassium chloride, sodium chloride and glucose directly into the bloodstream. Potassium chloride increases extracellular potassium, supporting cardiac and muscular function. Sodium chloride restores sodium balance and extracellular fluid volume. Glucose provides metabolic energy and stimulates insulin release, which promotes intracellular potassium uptake, helping to normalize electrolyte distribution and cellular function.

Side Effects

Kalium-Natrium-Glucose Braun may cause a range of adverse reactions.

Common Side Effects

  • Injection site pain: mild discomfort at the infusion site.
  • Erythema: localized redness around the injection area.
  • Mild hyperkalemia: slight elevation of serum potassium.
  • Mild hypernatremia: slight elevation of serum sodium.
  • Nausea: transient feeling of queasiness.
  • Headache: mild to moderate head discomfort.

Serious or Rare Side Effects

  • Severe hyperkalemia: significant potassium rise leading to cardiac arrhythmia.
  • Cardiac arrhythmia: irregular heart rhythm potentially life‑threatening.
  • Anaphylaxis: severe allergic reaction with respiratory compromise.
  • Severe hypernatremia: marked sodium increase causing neurological symptoms.
  • Metabolic acidosis: disturbance in acid‑base balance.
  • Thrombophlebitis: inflammation of a vein with clot formation.

Precautions & Warnings

Before administering Kalium-Natrium-Glucose Braun, consider the following precautions.

  • Assess electrolyte levels: verify baseline potassium and sodium concentrations.
  • Monitor cardiac rhythm: observe for arrhythmias during and after infusion.
  • Adjust for renal impairment: reduce dose or infusion rate in patients with reduced kidney function.
  • Use caution in heart failure: avoid rapid volume expansion.
  • Avoid rapid infusion: administer at recommended rate to prevent electrolyte shifts.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Kalium-Natrium-Glucose Braun can interact with other medications affecting electrolyte balance.

Major Interactions (Avoid)

  • ACE inhibitors: may potentiate hyperkalemia.
  • Potassium‑sparing diuretics: increase risk of elevated potassium levels.
  • NSAIDs: can reduce renal clearance of electrolytes.
  • IV calcium gluconate: may precipitate when mixed.
  • Digoxin: heightened risk of toxicity with electrolyte disturbances.

Moderate Interactions (Monitor Closely)

  • Insulin: enhances cellular uptake of potassium, may require dose adjustment.
  • Beta‑blockers: can mask signs of hypoglycemia.
  • Loop diuretics: may cause additional electrolyte loss.
  • Corticosteroids: influence sodium retention.
  • Anticoagulants: monitor for bleeding if infusion causes vein irritation.

Frequently Asked Questions

Kalium-Natrium-Glucose Braun is an injectable electrolyte solution used to replace potassium, sodium and glucose in patients with electrolyte deficiencies, dehydration, hypokalemia, hyponatremia, or those requiring fluid therapy after surgery.

The formulation delivers potassium chloride to raise serum potassium, sodium chloride to restore sodium balance and extracellular fluid volume, and glucose to provide metabolic energy while stimulating insulin‑mediated intracellular potassium uptake, together helping to normalize electrolyte distribution.

The dose is individualized and set by the prescribing clinician based on the patient’s electrolyte status, weight, renal function and clinical condition. Healthcare professionals determine the appropriate volume and infusion rate.

Safety data for use in pregnancy or lactation are limited. The product should only be used if the potential benefit justifies any potential risk to the fetus or infant, and the decision must be made by the treating physician.

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 needed) and import documentation.

Compared with simple saline solutions, Kalium-Natrium-Glucose Braun adds potassium and glucose, offering a more comprehensive electrolyte and energy replacement. This can be advantageous in patients needing simultaneous potassium repletion and metabolic support, whereas plain saline lacks these components.

The product 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 to maintain sterility and stability.

It is administered by intravenous or subcutaneous injection under aseptic conditions. The infusion rate and total volume are determined by the prescriber, and the solution should be administered using compatible IV sets and filters as recommended.

Serious risks include severe hyperkalemia or hypernatremia, which can lead to cardiac arrhythmias, anaphylactic reactions, metabolic acidosis, and thrombophlebitis. Prompt monitoring of electrolyte levels and cardiac function is essential during therapy.

Patients with known hypersensitivity to any component, uncontrolled hyperkalemia or hypernatremia, severe renal failure without appropriate dose adjustment, or those receiving contraindicated medications (e.g., potassium‑sparing diuretics) should not receive this product unless closely supervised by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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