Product image of Glucose-Na-K Baxter (Magnesium Chloride Hexahydrate, Potassium Chloride, Sodium Chloride, Glucose, Sodium Acetate Trihydr) supplied by GNH India

Glucose-Na-K Baxter

Active Ingredient:
Magnesium Chloride Hexahydrate, Potassium Chloride, Sodium Chloride, Glucose, Sodium Acetate Trihydr
Origin:
EU

Glucose-Na-K Baxter (Magnesium Chloride Hexahydrate, Potassium Chloride, Sodium Chloride, Glucose, Sodium Acetate Trihydr)

Glucose-Na-K Baxter is an intravenous solution containing magnesium chloride hexahydrate, potassium chloride, sodium chloride, glucose, and sodium acetate trihydrate. Formulated for fluid and electrolyte replacement, it delivers water, electrolytes and glucose directly into the bloodstream. The product is supplied in a sterile liquid form and is marketed in the European Union for use under prescription by healthcare professionals.

Manufacturer / TM Owner

Baxter Medical Ab

1
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Indications & Clinical Uses

Glucose-Na-K Baxter is indicated for clinical situations that require rapid volume expansion and electrolyte repletion. It is commonly employed in the following contexts:

  • Treatment of dehydration caused by gastrointestinal losses or inadequate oral intake.
  • Support during surgery or invasive procedures to maintain intravascular volume.
  • Management of electrolyte imbalances such as hypokalemia, hyponatremia, or hypomagnesemia.
  • Provision of metabolic substrate (glucose) in patients unable to receive enteral nutrition.
  • Adjunct therapy in critical care settings for patients with shock or sepsis.

Side Effects

Adverse reactions to Glucose-Na-K Baxter are generally related to its electrolyte composition and infusion characteristics.

Common

  • Mild infusion site irritation or phlebitis.
  • Transient hyperglycemia.
  • Slight electrolyte shifts (e.g., mild hyperkalemia).
  • Nausea or vomiting.
  • Headache.
  • Flushing or warmth at the infusion site.

Serious

  • Severe hyperkalemia leading to cardiac arrhythmia.
  • Hypermagnesemia causing respiratory depression.
  • Anaphylactic or severe allergic reaction.
  • Volume overload with pulmonary edema.
  • Metabolic acidosis from acetate accumulation.
  • Hemolysis due to rapid infusion rates.

Precautions & Warnings

When administering Glucose-Na-K Baxter, clinicians should observe several safety considerations. Proper patient assessment and monitoring are essential to minimize risks.

  • Verify electrolyte levels and renal function before initiation.
  • Adjust infusion rate to avoid rapid volume expansion.
  • Monitor cardiac rhythm in patients at risk for hyperkalemia.
  • Use caution in patients with heart failure or fluid overload.
  • Assess for signs of allergic reaction during the first infusion.
  • Ensure compatibility with other IV solutions and medications.
  • Document infusion parameters and patient response accurately.

Avoid Interactions

Glucose-Na-K Baxter may interact with other medications that affect electrolyte balance or fluid status. Awareness of these interactions helps prevent complications.

Avoid

  • Concurrent administration of high-dose potassium supplements without monitoring.
  • Use of other magnesium-containing IV solutions that could cause hypermagnesemia.
  • Co‑infusion with acidic drugs that may precipitate salts.

Use with caution

  • Loop diuretics, which can alter potassium and magnesium levels.
  • ACE inhibitors or ARBs, which may increase serum potassium.
  • Insulin therapy, which can shift glucose and potassium intracellularly.
  • Blood transfusions, which may affect calcium and magnesium balance.

Frequently Asked Questions

Glucose-Na-K Baxter is designed to provide rapid volume expansion, replace electrolytes, and supply glucose for metabolic support through intravenous administration.

The solution contains magnesium, potassium, sodium, and acetate ions, along with glucose as an energy source.

Use in children should be determined by a qualified healthcare professional, taking into account age‑specific dosing and electrolyte requirements.

The infusion rate should be individualized based on the patient’s volume status, cardiac function, and electrolyte levels, and it must be monitored continuously.

Regular assessment of vital signs, cardiac rhythm, serum electrolytes, glucose, and fluid balance is recommended throughout the infusion.

Compatibility depends on the specific medication; clinicians should consult compatibility charts and avoid mixing with acidic drugs that may cause precipitation.

Symptoms may include rash, itching, swelling, difficulty breathing, or hypotension, and require immediate medical attention.

Patients with reduced kidney function need careful electrolyte monitoring and may require dose adjustments or alternative therapies.

The infusion should be stopped, potassium levels re‑checked, and appropriate treatment for hyperkalemia initiated according to clinical guidelines.

Yes, it is classified as a prescription‑only product and must be administered by qualified healthcare personnel.

The solution should be stored at controlled room temperature, protected from light, and used before the expiration date indicated on the packaging.

The product is classified under ATC code B05AA, which corresponds to solutions for parenteral nutrition and fluid replacement.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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