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Glucosio E Sodio Cloruro Ii Galenica Senese

Active Ingredient:
Sodium Chloride, Glucose Monohydrate
Origin:
EU

Glucosio E Sodio Cloruro Ii Galenica Senese (Sodium Chloride, Glucose Monohydrate)

Glucosio E Sodio Cloruro Ii Galenica Senese is an injectable solution that contains sodium chloride and glucose monohydrate. It is supplied as a sterile intravenous fluid without a specified strength label. The preparation is classified as an electrolyte solution and is intended for use under medical supervision. It belongs to the volume expander and electrolyte replenisher therapeutic class and is marketed in the European Union.

Manufacturer / TM Owner

Industria Farmaceutica Galenica Senese S.R.L..

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Indications & Clinical Uses

Glucosio E Sodio Cloruro Ii Galenica Senese is used in clinical settings to manage fluid and electrolyte balance and to provide an energy source.

  • Replacement of extracellular fluid losses due to dehydration, surgery, or trauma.
  • Correction of hyponatremia or other electrolyte disturbances.
  • Treatment of hypoglycemia when rapid glucose delivery is required.
  • Support of parenteral nutrition regimens as a source of glucose and sodium chloride.
  • Adjunctive therapy during blood transfusion to maintain circulatory volume.

Side Effects

The safety profile of the sodium chloride and glucose injection reflects the expected reactions to intravenous electrolyte solutions.

Common

  • Mild pain or irritation at the injection site.
  • Transient increase in blood sodium levels.
  • Temporary rise in blood glucose concentration.
  • Mild nausea or vomiting.

Serious

  • Hypernatremia leading to neurological symptoms.
  • Severe hyperglycemia or diabetic ketoacidosis in susceptible patients.
  • Fluid overload causing pulmonary edema.
  • Allergic or anaphylactic reaction to the solution components.

Precautions & Warnings

Clinicians should evaluate patient-specific factors before administering Glucosio E Sodio Cloruro Ii Galenica Senese.

  • Assess baseline electrolyte and glucose levels to avoid overcorrection.
  • Use caution in patients with heart failure, renal impairment, or pulmonary disease due to risk of fluid overload.
  • Monitor for signs of hypernatremia or hyperglycemia during and after infusion.
  • Adjust infusion rate in neonates, infants, and the elderly.
  • Avoid rapid administration in patients with compromised vascular integrity.
  • Discontinue if an allergic reaction is suspected.

Avoid Interactions

The intravenous solution may interact with other medications or clinical conditions.

Avoid

  • Concomitant administration of hypertonic saline or high‑dose glucose solutions, which can exacerbate electrolyte imbalance.
  • Use with drugs that may cause fluid retention, such as corticosteroids, without careful monitoring.

Use with caution

  • Diuretics, which can alter sodium balance and require electrolyte monitoring.
  • Insulin therapy, because rapid glucose infusion may affect glycemic control.
  • Cardiac glycosides, where changes in serum electrolytes can influence drug toxicity.
  • Anticoagulants, as large-volume infusions may affect coagulation parameters.

Frequently Asked Questions

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

It is indicated for fluid and electrolyte replacement, treatment of hypoglycemia, and as part of parenteral nutrition support.

The product is given by intravenous infusion under medical supervision, typically through a peripheral or central line.

Yes, but dosing and infusion rates must be adjusted for age, weight, and clinical condition, and close monitoring is required.

Serum sodium, glucose, and overall fluid balance should be checked before, during, and after infusion.

If administered in excess or without proper monitoring, sodium overload can lead to hypernatremia, which may cause neurological symptoms.

Common side effects include mild pain at the injection site, transient increases in serum sodium or glucose, and occasional nausea or vomiting.

Serious reactions include severe hypernatremia, marked hyperglycemia, fluid overload with pulmonary edema, and allergic or anaphylactic responses.

Caution is advised; patients with heart failure are at higher risk for fluid overload and should be closely monitored.

Mixing is generally discouraged unless compatibility has been confirmed, as incompatibility can affect drug stability and patient safety.

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

Store the unopened vials in a cool, dry place away from direct sunlight, and protect from freezing.

Published by

GNH India Pharmaceuticals Limited

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Last updated:

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