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Glucosalino Hiposódico

Active Ingredient:
Sodium Chloride, Glucose Monohydrate
Origin:
EU

Glucosalino Hiposódico (Sodium Chloride, Glucose Monohydrate)

Glucosalino Hiposódico is an intravenous solution that combines sodium chloride and glucose monohydrate in a balanced formulation designed for fluid and electrolyte replacement. The product is supplied as a sterile solution for IV administration and is marketed in the European Union. It is prescribed by healthcare professionals for patients who require controlled sodium and glucose delivery to support extracellular fluid volume and metabolic needs in clinical practice.

Manufacturer / TM Owner

B.Braun Medical, S.A.

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Indications & Clinical Uses

Glucosalino Hiposódico is indicated for several clinical situations where fluid, electrolyte, or glucose supplementation is required.

  • Replacement of extracellular fluid losses due to dehydration, burns, or gastrointestinal fluid loss.
  • Maintenance of sodium and chloride balance during peri‑operative or intensive‑care management.
  • Treatment of mild to moderate hypoglycemia when combined with dextrose therapy.
  • Support of patients receiving parenteral nutrition who need additional sodium and glucose.
  • Rehydration of patients with electrolyte disturbances such as hyponatremia or hypochloremia.
  • Use in emergency or trauma settings to provide rapid intravascular volume expansion and osmotic support.

Side Effects

Adverse reactions to Glucosalino Hiposódico are generally related to the infusion of electrolytes and glucose and may vary in frequency and severity.

Common

  • Mild infusion site irritation or erythema.
  • Transient hypernatremia or hyperglycemia that resolves with monitoring.
  • Nausea or mild abdominal discomfort.
  • Transient increase in blood glucose level.
  • Mild headache or dizziness during rapid infusion.

Serious

  • Severe electrolyte imbalance such as hypernatremia, hyponatremia, or hyperchloremia.
  • Allergic reaction including urticaria, bronchospasm, or anaphylaxis.
  • Volume overload leading to pulmonary edema.
  • Metabolic acidosis in patients with impaired glucose metabolism.
  • Cardiac arrhythmias associated with rapid shifts in serum sodium.
  • Renal impairment exacerbated by high sodium load.

Precautions & Warnings

When prescribing Glucosalino Hiposódico, clinicians should evaluate patient-specific factors and monitor relevant parameters to minimize risks.

  • Assess baseline serum electrolytes and glucose before initiation.
  • Adjust infusion rate in patients with cardiac or renal insufficiency to avoid volume overload.
  • Use caution in individuals with known hypersensitivity to sodium chloride or glucose solutions.
  • Monitor blood pressure and fluid balance during and after administration.
  • Avoid rapid bolus administration unless clinically indicated for emergency resuscitation.
  • Re‑evaluate therapy regularly in neonates, elderly, or critically ill patients.

Avoid Interactions

Glucosalino Hiposódico may interact with other intravenous therapies or medications that affect fluid, electrolyte, or glucose balance.

Avoid

  • Co‑administration with hypertonic saline solutions, which can cause excessive sodium load.
  • Simultaneous infusion of high‑dose dextrose preparations that may lead to severe hyperglycemia.
  • Concurrent use with potassium chloride solutions, which may cause hyperkalemia when combined with sodium load.

Use with caution

  • Loop diuretics, as they can exacerbate electrolyte shifts during therapy.
  • ACE inhibitors or ARBs, which may alter renal handling of sodium and potassium.
  • Vasopressors, because rapid volume changes can affect hemodynamic response.
  • Insulin therapy, as glucose infusion can modify insulin requirements and risk of hypoglycemia.

Frequently Asked Questions

Glucosalino Hiposódico contains sodium chloride and glucose monohydrate dissolved in a sterile aqueous solution for intravenous administration.

It is used for fluid replacement, maintaining electrolyte balance, treating mild to moderate hypoglycemia, and providing peri‑operative hydration.

The product is supplied as an intravenous solution and is administered through a controlled IV infusion under medical supervision.

Use in neonates and children should be based on clinical judgment, with careful monitoring of electrolyte and glucose levels.

Baseline and periodic checks of serum sodium, chloride, glucose, blood pressure, and fluid balance are recommended.

It should not be mixed with hypertonic saline or high‑dose dextrose solutions in the same line without proper flushing to avoid incompatibility.

Common side effects include mild infusion site irritation, transient changes in blood sodium or glucose, nausea, headache, or mild dizziness.

Avoid in patients with known hypersensitivity to its components or when concurrent administration of hypertonic saline or high‑dose dextrose could cause electrolyte overload.

The glucose component provides a rapid source of carbohydrate, helping to raise blood glucose levels when combined with appropriate clinical protocols.

Yes, it is classified as a prescription‑only (Rx) product and must be prescribed by a qualified healthcare professional.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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