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Glucose Fresenius

Active Ingredient:
Glucose Monohydrate
Origin:
EU

Glucose Fresenius (Glucose Monohydrate)

Glucose Fresenius is a sterile intravenous solution for injection that contains glucose monohydrate as its active ingredient. Manufactured for the European market, this excipient‑type product provides a readily available source of carbohydrate in a liquid form. It is supplied as a clear, isotonic solution intended for infusion or bolus administration in clinical settings where rapid glucose delivery is required to patients undergoing surgery or critical care.

Manufacturer / TM Owner

Fresenius Kabi France S.A.S.

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Indications & Clinical Uses

Glucose Fresenius is used in clinical practice primarily as an intravenous carbohydrate source and solvent for drug dilution.

  • To provide rapid energy to patients with hypoglycemia or during peri‑operative fasting.
  • As a carrier solution for the reconstitution of lyophilized medications administered intravenously.
  • For maintenance of fluid and electrolyte balance in patients requiring parenteral nutrition.
  • To correct or prevent low blood glucose levels during critical care or trauma resuscitation.
  • As an osmotic agent in certain diagnostic or therapeutic infusion protocols.

Side Effects

Adverse reactions to Glucose Fresenius are generally infrequent, but they can be categorized by frequency and severity.

Common

  • Mild local irritation or erythema at the infusion site.
  • Transient hyperglycemia, especially with rapid or large-volume administration.
  • Nausea or a feeling of warmth during infusion.
  • Headache or dizziness related to rapid changes in blood glucose.
  • Transient increase in serum osmolality causing mild thirst.

Serious

  • Severe hyperglycemia leading to osmotic diuresis or electrolyte disturbances.
  • Hypersensitivity reactions such as urticaria, bronchospasm, or anaphylaxis.
  • Volume overload or pulmonary edema in patients with compromised cardiac function.
  • Acute renal impairment due to osmotic nephrosis in susceptible individuals.
  • Metabolic acidosis secondary to excessive glucose metabolism in rare cases.

Precautions & Warnings

When using Glucose Fresenius, clinicians should observe several precautionary measures to minimize risks and ensure appropriate patient selection.

  • Assess baseline blood glucose and monitor levels frequently during and after infusion.
  • Adjust infusion rate in patients with diabetes, renal insufficiency, or heart failure to avoid hyperglycemia or fluid overload.
  • Use aseptic technique to prevent contamination of the sterile solution.
  • Verify compatibility with co‑administered drugs, as high glucose concentrations may affect stability.
  • Avoid rapid large-volume boluses unless clinically indicated.
  • Consider electrolyte status, particularly sodium and potassium, before administration.
  • Document infusion parameters and patient response in the medical record.

Avoid Interactions

Glucose Fresenius may interact with certain medications or clinical conditions, requiring careful consideration of compatibility and patient status.

Avoid

  • Co‑administration with insulin or other hypoglycemic agents without adjusting doses, to prevent severe hypoglycemia.
  • Simultaneous infusion of high‑concentration dextrose solutions with calcium‑containing medications, which can precipitate calcium phosphate.

Use with caution

  • Concurrent use of diuretics or antihypertensives in patients at risk of fluid overload.
  • Administration in patients receiving sodium‑containing fluids, to avoid hypernatremia.
  • Use in individuals on beta‑blockers, as altered glucose metabolism may mask hypoglycemia symptoms.

Frequently Asked Questions

Glucose Fresenius is a sterile solution for injection that contains glucose monohydrate as its sole active ingredient, providing an intravenous source of carbohydrate.

It is administered intravenously, either as a continuous infusion or a rapid bolus, according to the clinical judgment of the healthcare provider.

It is commonly used to treat hypoglycemia, provide energy during peri‑operative fasting, serve as a diluent for reconstituting injectable drugs, and support fluid and electrolyte balance in parenteral nutrition.

Common adverse effects include mild local irritation at the infusion site, transient hyperglycemia, nausea, headache, dizziness, and a temporary increase in serum osmolality.

Serious reactions may involve severe hyperglycemia with osmotic diuresis, hypersensitivity such as urticaria or anaphylaxis, volume overload leading to pulmonary edema, acute renal impairment, or metabolic acidosis in rare cases.

Blood glucose levels should be measured before starting the infusion and monitored regularly during and after administration to detect any rapid changes.

Compatibility should be confirmed for each medication, as high concentrations of glucose can affect the stability of some drugs; consult compatibility charts or pharmacy resources.

Patients with diabetes require careful monitoring of glucose levels and possible adjustment of insulin or other hypoglycemic agents to avoid excessive hyperglycemia.

Avoid concurrent administration with insulin or other hypoglycemic agents without dose adjustment, and be cautious when mixing with calcium‑containing solutions due to precipitation risk.

The solution should be stored at controlled room temperature, protected from light, and kept in its original sealed container until ready for administration.

The infusion rate is determined by the treating clinician based on the patient’s clinical condition, blood glucose level, and overall fluid management plan.

Glucose Fresenius is typically classified as a prescription‑only product and is administered under the supervision of qualified healthcare professionals.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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