Product image of Glucosio Baxter S.P.A. (Glucose Monohydrate) supplied by GNH India

Glucosio Baxter S.P.A.

Active Ingredient:
Glucose Monohydrate
Origin:
EU

Glucosio Baxter S.P.A. (Glucose Monohydrate)

Glucosio Baxter S.P.A. is an intravenous solution for injection that contains glucose monohydrate as the active ingredient. It is supplied in a sterile aqueous solution form, marketed in the European Union and available by prescription. The product provides a readily available source of glucose for patients requiring parenteral nutrition or rapid correction of low blood sugar levels and can be administered under controlled clinical conditions.

Manufacturer / TM Owner

Baxter S.P.A.

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Indications & Clinical Uses

Glucosio Baxter is indicated for clinical situations where an immediate source of carbohydrate is required.

  • Parenteral nutrition as part of total nutrient admixtures for patients unable to receive enteral feeding.
  • Treatment of acute hypoglycemia in emergency or perioperative settings.
  • Support during prolonged fasting or pre‑operative fasting when oral intake is not possible.
  • Dilution and compatible mixing with other intravenous medications for fluid replacement.
  • Management of glucose requirements in critically ill patients under intensive care monitoring.

Side Effects

Glucosio Baxter may be associated with infusion‑related reactions, although many patients tolerate the solution without notable events.

Common

  • Local irritation at the injection site
  • Transient hyperglycemia
  • Mild electrolyte shifts (e.g., sodium, potassium)
  • Nausea or mild abdominal discomfort

Serious

  • Severe hyperglycemia leading to osmotic diuresis
  • Allergic or anaphylactic reaction to the solution components
  • Fluid overload causing pulmonary edema
  • Metabolic acidosis in susceptible patients

Precautions & Warnings

When prescribing Glucosio Baxter, clinicians should evaluate patient‑specific factors and monitor for potential complications.

  • Assess blood glucose levels before and during infusion to avoid excessive hyperglycemia.
  • Use caution in patients with diabetes mellitus, renal impairment, or heart failure.
  • Adjust infusion rate in neonates, infants, and pediatric patients due to different metabolic rates.
  • Monitor fluid balance and electrolytes, especially sodium and potassium, during prolonged administration.
  • Avoid rapid bolus administration unless clinically indicated.
  • Verify compatibility with other intravenous solutions to prevent precipitation.
  • Document any adverse reactions in the patient’s medical record.

Avoid Interactions

Glucosio Baxter can interact with other agents administered intravenously or affect systemic metabolic pathways.

Avoid

  • Concurrent high‑dose insulin infusions without glucose monitoring, which may precipitate severe hypoglycemia.
  • Co‑administration with other hypertonic glucose solutions, increasing risk of hyperosmolar complications.
  • Use with potassium‑rich solutions without electrolyte monitoring, risking hyperkalemia.

Use with caution

  • Simultaneous administration of diuretics that may alter fluid and electrolyte status.
  • Concurrent use of corticosteroids, which can raise blood glucose levels.
  • Combination with beta‑adrenergic agonists that may affect glucose metabolism.

Frequently Asked Questions

Glucosio Baxter provides an immediate source of glucose for patients who need parenteral nutrition or rapid correction of low blood sugar levels.

The product is supplied as a sterile aqueous solution for intravenous injection and is administered through a controlled infusion set.

Yes, but infusion rates should be adjusted for neonates, infants, and children because their metabolic requirements differ from adults.

Blood glucose, electrolyte levels, and fluid balance should be regularly monitored to avoid hyperglycemia, electrolyte disturbances, or fluid overload.

Compatibility should be confirmed for each co‑administered drug; the solution can be mixed with many IV fluids, but incompatibilities may cause precipitation.

Common effects include mild local irritation, transient hyperglycemia, mild electrolyte shifts, and occasional nausea or abdominal discomfort.

It should be avoided in patients with uncontrolled severe hyperglycemia, known allergy to the formulation, or when rapid bolus administration would pose a risk.

Glucosio Baxter is delivered directly into the bloodstream, providing immediate glucose availability, whereas oral preparations require gastrointestinal absorption.

Concurrent high‑dose insulin without proper glucose monitoring can cause severe hypoglycemia; dosage adjustments and close monitoring are essential.

Yes, Glucosio Baxter is classified as a prescription‑only medication (Rx) in the European Union.

It can be part of fluid replacement regimens when glucose supplementation is needed, but total fluid volume and electrolyte composition must be considered.

The infusion should be stopped immediately, and appropriate emergency measures, such as administration of antihistamines or epinephrine, should be initiated.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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