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Glucose Fresenius Kabi

Active Ingredient:
Glucose Monohydrate
Origin:
EU

Glucose Fresenius Kabi (Glucose Monohydrate)

Glucose Fresenius Kabi is an intravenous solution containing glucose monohydrate as the active ingredient; the product’s strength and concentration are not specified in the available data, and it is supplied as a sterile parenteral fluid for clinical use in the European market. It is intended for administration by healthcare professionals under controlled conditions and is classified as an excipient/carbohydrate solution within the parenteral nutrition and fluid replacement therapeutic categories.

Manufacturer / TM Owner

Fresenius Kabi S.R.O.

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Indications & Clinical Uses

Glucose Fresenius Kabi is used in clinical settings to provide rapid carbohydrate supplementation and to support fluid balance when oral intake is insufficient or contraindicated.

  • Treatment of hypoglycemia when intravenous glucose is required.
  • Component of parenteral nutrition regimens to supply caloric energy.
  • Fluid and electrolyte replacement in perioperative or critical‑care patients.
  • Dilution medium for compatible intravenous medications.
  • Support for patients with prolonged fasting or malnutrition.
  • Maintenance of blood glucose levels during insulin therapy adjustments.

Side Effects

When administered intravenously, glucose solutions can produce a range of physiological responses. Most are mild and transient, while rare events may require medical attention.

Common

  • Transient hyperglycemia that resolves with monitoring.
  • Mild nausea or vomiting.
  • Local irritation or erythema at the infusion site.
  • Electrolyte shifts such as mild hypokalemia.

Serious

  • Severe hyperglycemia leading to osmotic diuresis.
  • Hypotension from rapid infusion of large volumes.
  • Allergic or anaphylactic reactions.
  • Metabolic acidosis in patients with impaired metabolism.

Precautions & Warnings

Glucose Fresenius Kabi should be administered only after evaluating the patient’s clinical status and laboratory values to avoid complications.

  • Verify blood glucose level before infusion to prevent excessive hyperglycemia.
  • Adjust infusion rate in patients with renal or cardiac insufficiency.
  • Use aseptic technique to maintain sterility of the solution.
  • Monitor electrolytes, especially potassium and phosphate, during prolonged therapy.
  • Avoid rapid administration of large volumes to reduce risk of circulatory overload.
  • Consider compatibility with other IV drugs; incompatibility may cause precipitation.

Avoid Interactions

Glucose solutions can interact with other intravenous agents or affect metabolic pathways, requiring careful coordination with concurrent therapies.

Avoid

  • Co‑administration with high‑dose insulin without appropriate glucose monitoring.
  • Mixing with calcium‑containing solutions that may precipitate.
  • Simultaneous infusion with certain parenteral lipid emulsions that can cause phase separation.

Use with caution

  • Concurrent use of diuretics that may exacerbate electrolyte disturbances.
  • Administration alongside catecholamines, which can increase glucose production.
  • Patients receiving beta‑blockers, as hypoglycemia symptoms may be masked.

Frequently Asked Questions

Glucose Fresenius Kabi is a sterile intravenous solution whose sole active ingredient is glucose monohydrate, providing a carbohydrate source for patients who require parenteral nutrition or fluid replacement.

It is commonly used for the treatment of hypoglycemia, as a component of total parenteral nutrition, and for fluid and electrolyte replacement in peri‑operative, intensive‑care, or fasting patients.

The product is administered by a healthcare professional through a peripheral or central intravenous line, with the infusion rate adjusted according to the patient’s blood‑glucose level and overall fluid requirements.

Common side effects include transient hyperglycemia, mild nausea or vomiting, local irritation at the infusion site, and mild electrolyte shifts such as hypokalemia.

Providers should regularly check blood‑glucose concentrations, monitor vital signs, assess electrolyte panels (especially potassium and phosphate), and observe the infusion site for signs of irritation or infection.

Compatibility depends on the specific medication; it can be used as a diluent for many drugs, but it should not be mixed with calcium‑containing solutions or certain lipid emulsions that may precipitate.

Infusion rates should be reduced, total fluid volume limited, and frequent monitoring of renal function and cardiac status performed to avoid fluid overload or electrolyte imbalance.

Rapid infusion of glucose can cause shifts in electrolytes, particularly lowering serum potassium and phosphate; ongoing electrolyte monitoring is recommended during prolonged therapy.

The solution can be used in pediatric care when dosed appropriately, but dosing calculations and monitoring must be performed by qualified clinicians familiar with pediatric fluid and glucose requirements.

Store the unopened vials or bags at controlled room temperature, protected from light, and discard any product that appears discolored, cloudy, or has compromised packaging.

Intravenous glucose bypasses gastrointestinal absorption, delivering immediate carbohydrate calories directly into the bloodstream, whereas oral preparations rely on digestive processes and have a slower onset of action.

Glucose Fresenius Kabi is marketed in the EU as a medicinal product for parenteral use; its specific prescription status may vary by member state, but it is generally available only under medical supervision.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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