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Glucose Laboratoire Aguettant

Active Ingredient:
Glucose
Origin:
EU

Glucose Laboratoire Aguettant (Glucose)

Glucose Laboratoire Aguettant is an intravenous glucose solution supplied as a prescription‑only product in the European market. The preparation contains glucose as the sole active ingredient and is provided in a sterile liquid form for parenteral administration. It is manufactured by Laboratoire Aguettant and is intended for use under medical supervision to support patients who require intravenous carbohydrate supplementation in settings such as surgery or critical care.

Manufacturer / TM Owner

Laboratoire Aguettant

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Indications & Clinical Uses

Glucose Laboratoire Aguettant is used as an intravenous source of carbohydrate to provide energy and maintain blood glucose levels in various clinical situations.

  • Management of hypoglycemia when oral intake is not possible.
  • Provision of caloric support during peri‑operative fasting.
  • Maintenance of plasma glucose in patients receiving total parenteral nutrition.
  • Support for patients in intensive care units who have increased metabolic demands.
  • Replacement of fluid and electrolytes when combined with appropriate additives.

Side Effects

Adverse reactions to intravenous glucose solutions are generally infrequent, but they can be categorized by frequency and severity.

Common

  • Mild hyperglycemia (transient elevation of blood glucose).
  • Local irritation at the infusion site.
  • Nausea or vomiting.
  • Headache.

Serious

  • Severe hyperglycemia leading to osmotic diuresis.
  • Allergic or anaphylactic reaction to the solution components.
  • Electrolyte imbalance (e.g., hyponatremia) when administered in large volumes.
  • Thrombophlebitis at the catheter site.

Precautions & Warnings

When using Glucose Laboratoire Aguettant, clinicians should observe several precautions to ensure patient safety and therapeutic effectiveness.

  • Verify patient’s blood glucose level before and during infusion.
  • Adjust infusion rate according to individual metabolic needs and clinical condition.
  • Use aseptic technique to prevent contamination of the sterile solution.
  • Monitor for signs of fluid overload, especially in patients with cardiac or renal impairment.
  • Consider electrolyte status, as large volumes may affect sodium and potassium balance.
  • Avoid use in patients with known hypersensitivity to glucose solutions.

Avoid Interactions

Intravenous glucose can interact with other medications or clinical conditions, influencing both efficacy and safety.

Avoid

  • Co‑administration with insulin bolus doses without appropriate glucose monitoring.
  • Simultaneous infusion of high‑concentration dextrose with calcium‑containing solutions, which may cause precipitation.

Use with caution

  • Concurrent use of diuretics that may alter fluid and electrolyte balance.
  • Administration alongside medications that affect blood glucose, such as glucocorticoids or beta‑agonists.
  • Patients receiving parenteral nutrition containing other carbohydrate sources to prevent excess caloric intake.

Frequently Asked Questions

Glucose Laboratoire Aguettant contains glucose as the sole active ingredient dissolved in a sterile aqueous solution; excipients typically include water for injection and may include buffering agents in accordance with European pharmacopeial standards.

It is indicated for the treatment of hypoglycemia, provision of caloric support during peri‑operative fasting, maintenance of plasma glucose in patients receiving total parenteral nutrition, and support of critically ill patients with increased metabolic demands.

Use in pediatric patients is possible under strict medical supervision, with dosing and infusion rates adjusted to the child’s age, weight, and clinical condition.

Blood glucose levels should be measured before starting the infusion and periodically thereafter; additionally, fluid balance, electrolytes, and signs of hyperglycemia or fluid overload should be monitored.

Compatibility depends on the specific solution; it is generally compatible with isotonic saline and balanced electrolyte solutions, but caution is advised when mixing with calcium‑containing solutions due to potential precipitation.

The product should be stored at controlled room temperature, protected from light, and kept in its original sealed container until use.

Yes, it can be administered via a peripheral IV line, provided the infusion rate and concentration are appropriate for peripheral administration and the site is monitored for irritation.

The infusion should be stopped immediately, and appropriate medical treatment for an allergic reaction, such as antihistamines or epinephrine, should be initiated according to clinical protocols.

Yes, it is classified as a prescription‑only (Rx) product and must be prescribed and administered by qualified healthcare professionals.

Glucose Laboratoire Aguettant is delivered directly into the bloodstream via intravenous infusion, providing rapid elevation of blood glucose, whereas oral preparations require gastrointestinal absorption and have a slower onset of action.

Large volumes may lead to fluid overload, electrolyte disturbances, and severe hyperglycemia; therefore, infusion rates and total volume should be individualized and closely monitored.

It can be used in diabetic patients when clinically indicated, but blood glucose monitoring and insulin adjustments are essential to avoid hyperglycemia.

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GNH India Pharmaceuticals Limited

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Last updated:

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