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Glucose Laboratoire Aguettant

Active Ingredient:
Glucose Monohydrate
Origin:
EU

Glucose Laboratoire Aguettant (Glucose Monohydrate)

Glucose Laboratoire Aguettant is an intravenous solution containing glucose monohydrate as the active ingredient; the product is supplied in a typical concentration, though specific strength is not disclosed, and is marketed within the European Union. It is classified as an excipient rather than a therapeutic drug and is intended for use by healthcare professionals in hospitals or infusion centers to provide carbohydrate energy during intravenous therapy.

Manufacturer / TM Owner

Laboratoire Aguettant

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Indications & Clinical Uses

Glucose Laboratoire Aguettant is used as an intravenous carbohydrate source to maintain blood glucose levels and provide energy during various medical procedures. It is commonly employed in the following clinical situations:

  • During surgery or anesthesia to prevent hypoglycemia.
  • In patients receiving parenteral nutrition who require a glucose supply.
  • For correction of low blood sugar in acute care settings.
  • As a diluent or carrier for compatible intravenous medications.
  • In pediatric or neonatal care where glucose provision is essential.

Side Effects

When administered intravenously, glucose solutions can produce a range of physiological responses. Reported effects are grouped into common and serious categories.

Common

  • Transient increase in blood glucose concentration.
  • Mild electrolyte shifts, particularly sodium and potassium.
  • Local irritation or discomfort at the infusion site.
  • Nausea or mild abdominal discomfort.

Serious

  • Hyperglycemia leading to osmotic diuresis.
  • Severe allergic reaction such as anaphylaxis, though rare.

Precautions & Warnings

Glucose Laboratoire Aguettant should be administered with attention to patient-specific factors and clinical context. Key precautions include:

  • Verify patient’s blood glucose level before infusion.
  • Adjust infusion rate in patients with renal or cardiac insufficiency.
  • Avoid rapid infusion in neonates and infants.
  • Monitor electrolytes, especially sodium and potassium, during prolonged use.
  • Use aseptic technique to prevent contamination of the solution.
  • Discontinue if signs of hypersensitivity or severe hyperglycemia develop.

Avoid Interactions

Glucose solutions may interact with other intravenous agents or affect the pharmacokinetics of certain medications. Interactions are categorized as follows:

Avoid

  • Concurrent administration with high‑dose insulin without appropriate monitoring.
  • Co‑infusion with potassium chloride solutions that could precipitate.
  • Mixing with medications that are incompatible with dextrose solutions (e.g., certain antibiotics).

Use with caution

  • Patients receiving diuretics, as shifts in fluid balance may be amplified.
  • Individuals on beta‑blockers, which can mask hypoglycemia symptoms.

Frequently Asked Questions

The product contains glucose monohydrate as its sole active ingredient.

It is given as an intravenous infusion, typically through a peripheral or central venous line, under the supervision of a healthcare professional.

It is used during surgery, in parenteral nutrition, to treat acute hypoglycemia, as a diluent for compatible IV drugs, and in pediatric or neonatal care where glucose support is needed.

Common responses include a temporary rise in blood glucose, mild shifts in electrolytes, possible local irritation at the infusion site, and occasional nausea or mild abdominal discomfort.

Regular blood glucose measurements are recommended, especially during prolonged infusions, to detect and manage elevated glucose levels promptly.

Patients with renal or cardiac insufficiency, neonates, infants, and those on insulin therapy may need adjusted infusion rates or closer monitoring.

Check compatibility charts, avoid mixing with potassium chloride solutions that may precipitate, and do not combine with drugs known to be incompatible with dextrose solutions.

Yes, it can be used in children and neonates, but infusion rates should be carefully calculated and monitored to avoid rapid glucose spikes.

Signs include hives, swelling of the face or throat, difficulty breathing, and a sudden drop in blood pressure, which require immediate medical intervention.

Store the solution in a cool, dry place away from direct sunlight, and protect it from freezing; follow the manufacturer’s label for specific temperature ranges.

Use sterile gloves, disinfect the vial stopper with an alcohol swab, draw the solution with a sterile syringe, and avoid contaminating the infusion set.

IV glucose can cause mild shifts in sodium and potassium levels, so electrolytes should be monitored during extended infusions, especially in patients with existing imbalances.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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