Product image of Glukosalina I (Sodium Chloride, Glucose) supplied by GNH India

Glukosalina I

Active Ingredient:
Sodium Chloride, Glucose
Origin:
EU

Glukosalina I (Sodium Chloride, Glucose)

Glukosalina I is an intravenous injection solution that contains the active ingredients sodium chloride and glucose. It is supplied in a sterile liquid form for infusion into the bloodstream. The product is marketed in the European Union and is used as an electrolyte and carbohydrate source in clinical settings. Its composition provides isotonic fluid replacement and energy support during medical procedures.

Manufacturer / TM Owner

Hrvatski Zavod Za Transfuzijsku Medicinu

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Indications & Clinical Uses

Glukosalina I is employed in various clinical situations where fluid, electrolyte, and energy supplementation are required. It may be used for:

  • Intravenous rehydration in patients with fluid loss.
  • Maintenance of electrolyte balance during surgery.
  • Providing a source of glucose for patients unable to eat.
  • Dilution and administration of other intravenous medications.
  • Support during perioperative fasting periods.
  • Treatment of mild hypoglycemia under medical supervision.

Side Effects

Side effects of Glukosalina I are generally related to its components and route of administration.

Common

  • Mild local irritation at the infusion site.
  • Transient increase in blood glucose levels.
  • Slight electrolyte shifts, such as mild hypernatremia.
  • Headache or dizziness during rapid infusion.
  • Nausea or mild gastrointestinal discomfort.

Serious

  • Severe hyperglycemia in susceptible individuals.
  • Significant electrolyte imbalance (e.g., hypernatremia, hyperchloremia).
  • Allergic reaction presenting as rash, itching, or anaphylaxis.
  • Fluid overload leading to pulmonary edema.
  • Venous thrombosis at the catheter site.

Precautions & Warnings

When using Glukosalina I, healthcare professionals should consider several safety measures. Important precautions include:

  • Assessing the patient’s baseline electrolyte and glucose status before infusion.
  • Adjusting infusion rate in patients with cardiac or renal impairment to avoid fluid overload.
  • Monitoring blood glucose levels in diabetic patients.
  • Using aseptic technique to prevent infection at the injection site.
  • Avoiding rapid bolus administration unless clinically indicated.
  • Observing for signs of allergic reaction during and after infusion.
  • Documenting the total volume administered to prevent overhydration.

Avoid Interactions

Glukosalina I may interact with other medications or clinical conditions. Interactions to consider are:

Avoid

  • Co-administration with hypertonic glucose solutions that could exacerbate hyperglycemia.
  • Simultaneous use of high-dose sodium-containing drugs that may cause severe hypernatremia.
  • Intravenous potassium supplements without electrolyte monitoring.

Use with caution

  • Concurrent diuretics, which may alter fluid and electrolyte balance.
  • Insulin therapy, requiring close glucose monitoring.
  • Medications that affect renal function, such as ACE inhibitors.
  • Blood thinners, due to potential dilutional effects on coagulation parameters.

Frequently Asked Questions

Glukosalina I contains sodium chloride and glucose as its active pharmaceutical ingredients.

Glukosalina I is administered intravenously as an injection solution.

It is commonly used for intravenous rehydration, electrolyte balance during surgery, glucose provision for fasting patients, and as a diluent for other IV medications.

Yes, but blood glucose levels should be closely monitored, and the infusion rate may need adjustment.

Common side effects include mild local irritation, transient increases in blood glucose, slight electrolyte shifts, headache, dizziness, and mild nausea.

Serious reactions can include severe hyperglycemia, significant electrolyte imbalance, allergic reactions such as anaphylaxis, fluid overload, and venous thrombosis.

There are no absolute contraindications listed, but caution is advised in patients with severe electrolyte disorders, uncontrolled diabetes, or fluid overload risk.

The infusion rate should be individualized based on the patient’s fluid status, electrolyte levels, cardiac and renal function, and clinical indication.

Monitoring should include vital signs, fluid balance, electrolyte panels, and blood glucose levels, especially in at‑risk patients.

It can be used as a diluent for compatible IV drugs, but compatibility should be verified according to manufacturer guidelines.

Glukosalina I is a prescription‑only product and is not available over the counter.

Glukosalina I is marketed in the European Union.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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