Product image of Glucosum Et Natrium Chloratum 1:1 Fresenius (Sodium Chloride, Glucose Monohydrate) supplied by GNH India

Glucosum Et Natrium Chloratum 1:1 Fresenius

Active Ingredient:
Sodium Chloride, Glucose Monohydrate
Origin:
EU

Glucosum Et Natrium Chloratum 1:1 Fresenius (Sodium Chloride, Glucose Monohydrate)

Glucosum Et Natrium Chloratum 1:1 Fresenius is an intravenous injection solution that combines sodium chloride and glucose monohydrate in a 1:1 ratio. The product is supplied as a sterile solution for infusion, intended for fluid and electrolyte replenishment. It is marketed in the European Union and requires a prescription. The exact concentration of each component is not disclosed in the label.

Manufacturer / TM Owner

Fresenius Kabi Polska Sp. Z O.O.

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Indications & Clinical Uses

Glucosum Et Natrium Chloratum 1:1 Fresenius is used in clinical settings to restore fluid balance and provide an energy source when oral intake is insufficient.

  • Replacement of extracellular fluid losses due to surgery, trauma, or burns.
  • Correction of hyponatremia or other electrolyte disturbances.
  • Support of parenteral nutrition regimens by supplying glucose.
  • Maintenance of intravascular volume during diagnostic or therapeutic procedures.
  • Adjunctive therapy in patients receiving other intravenous medications that may cause electrolyte shifts.

Side Effects

Adverse reactions to Glucosum Et Natrium Chloratum 1:1 Fresenius are generally related to the infusion itself or the individual components.

Common

  • Mild infusion site irritation or erythema.
  • Transient hyperglycemia, especially in patients with impaired glucose tolerance.
  • Slight increase in serum sodium levels.
  • Fluid overload manifested as peripheral edema.

Serious

  • Severe hypernatremia leading to neurologic symptoms.
  • Anaphylactoid reactions such as urticaria, bronchospasm, or hypotension.
  • Metabolic acidosis in patients with compromised renal function.
  • Pulmonary edema due to excessive volume administration.

Precautions & Warnings

When prescribing or administering Glucosum Et Natrium Chloratum 1:1 Fresenius, clinicians should observe several safety considerations.

  • Verify patient’s electrolyte status and serum glucose before infusion.
  • Adjust infusion rate in patients with heart failure or renal insufficiency to avoid fluid overload.
  • Use aseptic technique to prevent contamination of the sterile solution.
  • Monitor vital signs and laboratory values during and after administration.
  • Avoid rapid bolus administration unless specifically indicated.
  • Consider alternative formulations for patients with known hypersensitivity to sodium chloride or glucose.

Avoid Interactions

Glucosum Et Natrium Chloratum 1:1 Fresenius may interact with other intravenous agents or systemic medications.

Avoid

  • Concurrent high‑dose insulin therapy without glucose monitoring, which can precipitate hypoglycemia.
  • Large volumes of other sodium‑containing solutions that may cause hypernatremia.
  • Medications that increase the risk of fluid overload, such as certain chemotherapeutic agents.

Use with caution

  • Diuretics, which may alter electrolyte balance and require closer monitoring.
  • Corticosteroids, which can affect glucose metabolism.
  • Vasopressors, as changes in intravascular volume may influence hemodynamic response.
  • Renal replacement therapies, where electrolyte shifts are common.

Frequently Asked Questions

It contains sodium chloride and glucose monohydrate combined in a 1:1 ratio, provided as a sterile injectable solution.

It is indicated for patients who need intravenous fluid and electrolyte replacement, such as those with dehydration, postoperative losses, or requiring parenteral nutrition.

The product is administered intravenously, typically by slow infusion, under the supervision of a healthcare professional.

Use in children should be based on clinical judgment, with dosing and monitoring adjusted for age, weight, and specific medical conditions.

Serum electrolytes (especially sodium), glucose level, and renal function should be evaluated prior to administration.

Common signs include peripheral edema, shortness of breath, and increased blood pressure; patients should be monitored closely.

Yes, transient hyperglycemia can occur, particularly in patients with impaired glucose tolerance or diabetes; glucose monitoring is recommended.

Infusion should be stopped immediately, and appropriate medical treatment for anaphylaxis or allergic reaction should be initiated.

Compatibility should be confirmed with each medication; some drugs may require separate lines to avoid precipitation or incompatibility.

The rate should be reduced and the patient closely monitored to prevent exacerbation of fluid overload and pulmonary edema.

No, it is a prescription‑only medication and must be administered by qualified healthcare personnel.

Store the solution at controlled room temperature, protected from light, and keep it out of reach of children.

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GNH India Pharmaceuticals Limited

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Last updated:

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