Product image of Glucosio Con Sodio Cloruro I Bioindustria L.I.M. (Sodium Chloride, Glucose Monohydrate) supplied by GNH India

Glucosio Con Sodio Cloruro I Bioindustria L.I.M.

Active Ingredient:
Sodium Chloride, Glucose Monohydrate
Origin:
EU

Glucosio Con Sodio Cloruro I Bioindustria L.I.M. (Sodium Chloride, Glucose Monohydrate)

Glucosio con Sodio Cloruro I Bioindustria L.I.M. is an injectable solution that combines sodium chloride and glucose monohydrate as its active ingredients. Formulated for intravenous administration, the product delivers electrolytes, carbohydrate energy, and metabolic support in a sterile liquid. It is marketed in the European Union and is available by prescription for use in clinical settings requiring fluid, electrolyte, or glucose support.

Manufacturer / TM Owner

Bioindustria Lim Laboratorio Italiano Medicinali Spa

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Indications & Clinical Uses

Glucosio con Sodio Cloruro I is indicated for several clinical situations where intravenous fluid, electrolyte, or glucose replacement is required.

  • Fluid and electrolyte replacement in patients with dehydration, surgery, or burns.
  • Treatment of hypoglycemia when oral glucose is not feasible.
  • Support of parenteral nutrition regimens as a source of carbohydrate and sodium chloride.
  • Maintenance of plasma volume during peri‑operative care.
  • Dilution and compatibility agent for certain intravenous medications.

Side Effects

Adverse reactions to the intravenous solution are generally infrequent, but they can be categorized by frequency and severity.

Common

  • Mild pain or irritation at the injection site.
  • Transient nausea or vomiting.
  • Temporary increase in blood glucose levels.
  • Mild electrolyte imbalance, such as slight hypernatremia.

Serious

  • Severe hypernatremia or hyperchloremia.
  • Allergic reactions such as urticaria, angioedema, or anaphylaxis.
  • Fluid overload leading to pulmonary edema.

Precautions & Warnings

When prescribing or administering Glucosio con Sodio Cloruro I, clinicians should observe several safety considerations.

  • Assess baseline electrolyte status and blood glucose before infusion.
  • Adjust infusion rate in patients with renal or cardiac impairment to avoid fluid overload.
  • Use caution in neonates, infants, and elderly patients due to altered fluid distribution.
  • Monitor for signs of hypernatremia, hyperchloremia, or rapid shifts in plasma osmolality.
  • Avoid concurrent rapid infusion of other high‑sodium solutions without dose recalculation.
  • Ensure sterility of the IV line to prevent infection.

Avoid Interactions

The solution may interact with other intravenous agents or systemic medications, influencing electrolyte balance or glucose levels.

Avoid

  • Co‑administration with other high‑sodium or hypertonic solutions without adjusting total sodium load.
  • Simultaneous infusion of potassium‑containing preparations that could cause abrupt electrolyte shifts.

Use with caution

  • Diabetic medications (e.g., insulin, oral hypoglycemics) because the glucose component may affect glycemic control.
  • Loop diuretics or thiazides, which alter sodium excretion.
  • Corticosteroids, which can increase sodium retention.
  • Blood transfusions, where rapid volume changes may exacerbate fluid balance issues.

Frequently Asked Questions

It provides intravenous sodium, chloride, and glucose to restore fluid and electrolyte balance and supply metabolic energy.

It is used for fluid and electrolyte replacement, treatment of hypoglycemia, and as a carbohydrate source in parenteral nutrition.

The product is administered intravenously as a sterile injection solution, typically through a peripheral or central line.

Use in neonates and infants should be cautious, with dosing and monitoring adjusted for age and weight.

Monitor blood electrolytes, glucose levels, fluid balance, and signs of overload or allergic reaction throughout the infusion.

Transient increases in blood glucose can occur; patients with diabetes may require additional glucose monitoring.

Contraindications include known hypersensitivity to sodium chloride or glucose and conditions where rapid sodium loading is unsafe.

Infusion rates should be reduced and fluid status closely monitored to avoid exacerbating fluid overload.

Compatibility should be verified; avoid mixing with other high‑sodium or hypertonic solutions unless the total sodium load is recalculated.

Store the unopened vials at controlled room temperature, protected from light, and discard after the expiration date.

Published by

GNH India Pharmaceuticals Limited

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Last updated:

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