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Glucose Fresenius

Active Ingredient:
Glucose
Origin:
EU

Glucose Fresenius (Glucose)

Glucose Fresenius is an intravenous solution for injection that contains the active ingredient glucose as its sole component. It is supplied in a sterile aqueous solution without a specified strength, and is classified as an excipient/solvent used in parenteral nutrition. The product is marketed in the European Union and requires a prescription. It provides a readily available carbohydrate source for patients needing intravenous energy support.

Manufacturer / TM Owner

Fresenius Kabi Austria Gmbh

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Indications & Clinical Uses

Glucose Fresenius is indicated for clinical situations where an intravenous carbohydrate source is required to maintain blood glucose levels and support nutritional needs, particularly when oral intake is limited or contraindicated. It is commonly incorporated into fluid therapy protocols and can be adjusted to meet individual caloric requirements.

  • Treatment of hypoglycemia when oral glucose is not feasible.
  • Component of total parenteral nutrition regimens.
  • Fluid and electrolyte replacement solutions.
  • Energy source during perioperative fasting.
  • Support for patients with impaired oral intake.
  • Used in pediatric and neonatal intensive care for glucose maintenance.

Side Effects

When administered intravenously, Glucose Fresenius may be associated with a range of adverse reactions that vary in frequency and severity. The frequency of these events depends on patient factors, infusion rate, and total carbohydrate load.

Common

  • Mild hyperglycemia or transient rise in blood glucose.
  • Local irritation at the infusion site.
  • Nausea or vomiting.
  • Electrolyte shifts such as mild hyponatremia.
  • Headache or dizziness during rapid infusion.
  • Mild metabolic acidosis in prolonged high‑dose therapy.

Serious

  • Severe hyperglycemia leading to osmotic diuresis.
  • Allergic reactions including rash, urticaria, or anaphylaxis.
  • Volume overload in patients with compromised cardiac function.
  • Hyperosmolar state with dehydration in patients receiving large volumes.

Precautions & Warnings

Glucose Fresenius should be used with attention to specific clinical considerations to minimize risks and ensure appropriate therapeutic outcomes.

  • Verify blood glucose levels before and during infusion.
  • Adjust infusion rate in patients with renal or hepatic impairment.
  • Monitor fluid balance to avoid volume overload.
  • Use caution in patients with diabetes mellitus or insulin resistance.
  • Assess electrolyte status, especially sodium and potassium, prior to administration.
  • Avoid rapid bolus administration unless clinically indicated, and monitor closely.
  • Consider compatibility with other intravenous solutions before mixing.

Avoid Interactions

When co‑administered carefully with other agents, Glucose Fresenius may affect or be affected by concurrent medications, requiring attention to potential interactions.

Avoid

  • Do not mix with calcium-containing solutions without compatibility testing.
  • Avoid simultaneous infusion with high‑dose insulin without appropriate glucose monitoring.

Use with caution

  • Use cautiously with diuretics that may alter electrolyte balance.
  • Monitor closely when combined with beta‑blockers that can mask hypoglycemia symptoms.
  • Adjust dosage when given with glucocorticoids that increase glucose production.
  • Be vigilant when co‑administered with vasopressors that may affect peripheral perfusion.
  • Consider glucose monitoring when combined with oral hypoglycemic agents.

Frequently Asked Questions

Glucose Fresenius provides an intravenous source of glucose to treat low blood sugar, support parenteral nutrition, and assist with fluid and electrolyte replacement.

It is commonly used in hospitals for patients with hypoglycemia, those receiving total parenteral nutrition, perioperative fasting, and in intensive care units where oral intake is limited.

Yes, it can be used in pediatric and neonatal intensive care when glucose maintenance is required, but dosing must be individualized by a healthcare professional.

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

Compatibility should be confirmed before mixing, especially with calcium‑containing solutions, to prevent precipitation or incompatibility reactions.

Common side effects include mild hyperglycemia, local infusion site irritation, nausea, vomiting, and minor electrolyte shifts such as hyponatremia.

Serious reactions may include severe hyperglycemia, allergic responses such as rash or anaphylaxis, volume overload, and hyperosmolar states leading to dehydration.

If insulin is administered concurrently, glucose infusion rates must be carefully adjusted and blood glucose monitored to avoid excessive hypoglycemia or hyperglycemia.

There are no absolute contraindications listed, but caution is advised in patients with uncontrolled diabetes, severe cardiac failure, or known hypersensitivity to glucose solutions.

It is supplied as a sterile aqueous solution for injection intended for intravenous administration under prescription.

Glucose Fresenius is classified as a prescription‑only medication (Rx) and is marketed within the European Union.

It can be part of fluid therapy to provide both volume and carbohydrate calories, but the overall fluid plan should be individualized.

Published by

GNH India Pharmaceuticals Limited

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Last updated:

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