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Glucose Com Cloreto De Sódio Basi

Active Ingredient:
Sodium Chloride, Glucose
Origin:
EU

Glucose Com Cloreto De Sódio Basi (Sodium Chloride, Glucose)

Glucose Com Cloreto De Sódio Basi is an intravenous injection solution that combines sodium chloride and glucose. The product is supplied in a sterile liquid form intended for infusion into the bloodstream. It is manufactured for the European market and is classified as an IV electrolyte and carbohydrate solution used to restore fluid volume, correct electrolyte disturbances, and provide metabolic energy.

Manufacturer / TM Owner

Laboratórios Basi – Indústria Farmacêutica, S.A.

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Indications & Clinical Uses

Glucose Com Cloreto De Sódio Basi is indicated for several clinical situations where fluid and electrolyte balance must be rapidly corrected. It is commonly employed in hospital settings for patients who cannot maintain adequate oral intake.

  • Replacement of extracellular fluid loss due to surgery, trauma, or burns.
  • Correction of hyponatremia or other electrolyte imbalances.
  • Prevention or treatment of hypoglycemia in patients unable to eat.
  • Support of metabolic needs during critical care or anesthesia.
  • Maintenance of hydration in patients receiving parenteral nutrition.

Side Effects

Adverse reactions to Glucose Com Cloreto De Sódio Basi are generally infrequent but can vary in severity.

Common

  • Mild infusion site irritation or pain.
  • Transient hyperglycemia.
  • Slight increase in serum sodium levels.
  • Nausea or mild vomiting.
  • Headache.
  • Low-grade fever.

Serious

  • Severe hypernatremia.
  • Acute hyperglycemic crisis.
  • Allergic reaction with rash, itching, or bronchospasm.
  • Fluid overload leading to pulmonary edema.
  • Electrolyte disturbances such as hyperchloremia.
  • Hemolysis from rapid infusion.

Precautions & Warnings

When using Glucose Com Cloreto De Sódio Basi, clinicians should observe several safety measures to minimize risk.

  • Verify patient’s electrolyte status and glucose level before administration.
  • Adjust infusion rate in patients with cardiac or renal insufficiency to avoid fluid overload.
  • Use caution in neonates and elderly patients due to altered fluid distribution.
  • Monitor serum sodium and glucose frequently during therapy.
  • Avoid rapid bolus administration; infuse over the recommended time.
  • Store the solution according to manufacturer guidelines to maintain sterility.

Avoid Interactions

Glucose Com Cloreto De Sódio Basi may interact with other medications administered intravenously.

Avoid

  • Concurrent infusion of hypertonic saline solutions that could exacerbate hypernatremia.
  • Co‑administration with high‑dose insulin without glucose monitoring, risking severe hypoglycemia.

Use with caution

  • Loop diuretics, which may increase sodium loss and require electrolyte monitoring.
  • Corticosteroids, which can raise blood glucose levels.
  • Vasopressors, where fluid volume changes may affect blood pressure control.
  • Other carbohydrate-containing IV solutions, to prevent excessive glucose load.
  • Medications that affect renal function, as they may alter electrolyte handling.

Frequently Asked Questions

The product is used to restore extracellular fluid volume, correct electrolyte imbalances, and provide metabolic energy through glucose.

It is frequently given during surgery, in intensive care units, after trauma or burns, and for patients who cannot take oral fluids.

Sodium chloride replenishes sodium ions, supporting osmotic balance and helping maintain blood pressure and nerve function.

Glucose supplies immediate metabolic energy and helps prevent or treat low blood sugar in patients unable to eat.

It may be used in children under careful dosing and monitoring, but clinicians should follow pediatric guidelines and adjust infusion rates.

Regular checks of serum sodium, glucose, and overall fluid balance are recommended, along with observation of infusion site for irritation.

Yes, especially in patients with heart or kidney disease; infusion rates should be individualized to avoid pulmonary edema.

A rash may indicate an allergic reaction; the infusion should be stopped and medical evaluation performed promptly.

Mixing is generally discouraged; separate lines or compatible solutions should be used to prevent incompatibility or precipitation.

It should be kept in a controlled environment, protected from light and extreme temperatures, and used before the expiration date.

The product is typically prescription‑only and administered by healthcare professionals in clinical settings.

Symptoms may include thirst, confusion, muscle twitching, and in severe cases, seizures or coma.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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