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Glucos Fresenius Kabi

Active Ingredient:
Glucose
Origin:
EU

Glucos Fresenius Kabi (Glucose)

Glucos Fresenius Kabi is an intravenous solution for injection that contains glucose as the sole active ingredient. It is supplied in a sterile solution form, marketed in the European Union, and classified as an excipient used to provide energy and maintain blood glucose levels during intravenous therapy. The product is prescription‑only and is commonly employed in clinical settings for fluid replacement, parenteral nutrition, and treatment of hypoglycemia.

Manufacturer / TM Owner

Fresenius Kabi Ab

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Indications & Clinical Uses

Glucos Fresenius Kabi is indicated for several clinical situations where rapid glucose delivery and fluid support are required.

  • Treatment of acute hypoglycemia in hospitalized patients.
  • Component of parenteral nutrition regimens for patients unable to eat orally.
  • Fluid replacement in patients with dehydration or electrolyte imbalance.
  • Support during surgical procedures requiring intravenous glucose.
  • Adjunct therapy for patients receiving medications that may lower blood glucose levels.

Side Effects

Glucos Fresenius Kabi may be associated with a range of adverse reactions, most of which are related to the intravenous administration of glucose.

Common

  • Mild hyperglycemia or transient rise in blood glucose.
  • Local irritation or pain at the infusion site.
  • Nausea or mild gastrointestinal discomfort.
  • Headache or dizziness during rapid infusion.
  • Electrolyte shifts, particularly potassium changes.

Serious

  • Severe hyperglycemia leading to osmotic diuresis.
  • Hypersensitivity reactions, including rash or urticaria.
  • Fluid overload causing pulmonary edema.
  • Hyperosmolar hyperglycemic state in susceptible patients.
  • Metabolic acidosis secondary to rapid glucose metabolism.

Precautions & Warnings

When using Glucos Fresenius Kabi, clinicians should consider several safety factors to minimize risk.

  • Assess baseline blood glucose and monitor levels frequently during infusion.
  • Adjust infusion rate in patients with renal or cardiac insufficiency to avoid fluid overload.
  • Use caution in patients with known hypersensitivity to glucose solutions or excipients.
  • Verify compatibility with other intravenous medications before co‑administration.
  • Consider electrolyte status, especially potassium and sodium, before and during therapy.
  • Document and report any unexpected adverse reactions promptly.

Avoid Interactions

Glucos Fresenius Kabi can interact with other agents administered intravenously or affect metabolic pathways.

Avoid

  • Concurrent infusion of high‑dose insulin without appropriate glucose monitoring.
  • Mixing with calcium‑containing solutions that may precipitate.
  • Co‑administration with medications that significantly lower blood glucose (e.g., sulfonylureas) without dose adjustment.

Use with caution

  • Concurrent use of diuretics that may alter fluid balance.
  • Administration alongside beta‑blockers, which can mask hypoglycemia symptoms.
  • Co‑infusion with potassium chloride solutions; monitor serum potassium.
  • Use in patients receiving total parenteral nutrition containing other carbohydrate sources.
  • Combination with vasopressors; monitor hemodynamic response.

Frequently Asked Questions

The solution is used to deliver glucose directly into the bloodstream to provide energy, correct low blood sugar, and support fluid balance during intravenous therapy.

It is commonly given in hospitals for treating hypoglycemia, as part of parenteral nutrition, during surgery, and for fluid replacement in dehydrated patients.

Blood glucose should be measured before starting the infusion and then at regular intervals, typically every 30–60 minutes, depending on the patient’s condition and infusion rate.

Compatibility should be confirmed for each medication; some drugs, especially calcium‑containing solutions, may precipitate when mixed with glucose solutions.

Serious reactions can include severe hyperglycemia, fluid overload with pulmonary edema, hypersensitivity rash or urticaria, and metabolic acidosis.

The product can be used in pediatric care, but dosing and infusion rates must be individualized by a qualified healthcare professional.

Patients with heart failure should have their fluid status closely monitored, and infusion rates may need to be reduced to avoid fluid overload.

When given with insulin, glucose infusion may counteract insulin’s blood‑sugar‑lowering effect, so glucose levels should be closely monitored and insulin doses adjusted as needed.

Rapid glucose infusion can cause shifts in potassium and sodium levels; electrolytes should be checked before and during therapy.

Yes, the product is classified as prescription‑only (Rx) and must be ordered by a licensed healthcare provider.

The solution should be stored at controlled room temperature, protected from light, and used before the expiration date indicated on the label.

It can be part of a long‑term parenteral nutrition regimen, but the overall formulation should be balanced with other nutrients and monitored regularly.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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