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Glucose Proamp Laboratoire Aguettant

Active Ingredient:
Glucose
Origin:
EU

Glucose Proamp Laboratoire Aguettant (Glucose)

Glucose Proamp Laboratoire Aguettant is an intravenous solution whose sole active ingredient is glucose. It is supplied in a sterile liquid form for infusion and is marketed in the European Union. The product provides a source of carbohydrate that can be used to support cellular energy metabolism when administered directly into the bloodstream.

Manufacturer / TM Owner

Laboratoire Aguettant

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Indications & Clinical Uses

Glucose Proamp is indicated for situations where rapid provision of carbohydrate energy is required. It is commonly employed in clinical settings for the following purposes:

  • Treatment of documented hypoglycemia in adults and children.
  • Component of parenteral nutrition regimens to supply calories.
  • Fluid replacement when combined with electrolytes.
  • Intra‑operative or peri‑operative glucose support.
  • Management of electrolyte disturbances associated with low blood glucose.

Side Effects

Side effects of intravenous glucose solutions are generally related to the metabolic and local effects of the infusion.

Common

  • Transient hyperglycemia or elevated blood glucose levels.
  • Local irritation or phlebitis at the infusion site.
  • Mild electrolyte shifts, particularly sodium and potassium.
  • Fluid overload when administered rapidly.
  • Nausea or abdominal discomfort.

Serious

  • Severe hyperglycemia leading to osmotic diuresis.
  • Anaphylactic or severe allergic reaction.
  • Cardiac arrhythmias associated with rapid glucose shifts.
  • Hyperosmolar hyperglycemic state in susceptible patients.
  • Acute renal dysfunction secondary to volume overload.

Precautions & Warnings

When using Glucose Proamp, clinicians should observe several safety measures to minimize risks. Important precautions include:

  • Regular monitoring of blood glucose concentrations during and after infusion.
  • Adjusting infusion rates in patients with renal or hepatic impairment.
  • Using aseptic technique to prevent catheter‑related infections.
  • Exercising caution in pregnant or breastfeeding individuals, as safety data are limited.
  • Evaluating pediatric patients carefully, with dose individualized by weight.
  • Avoiding rapid bolus administration unless clinically indicated.

Avoid Interactions

Glucose Proamp may interact with other agents that affect blood glucose or electrolyte balance.

Avoid

  • Concurrent high‑dose insulin or insulin analogues that could precipitate severe hypoglycemia.
  • Sulfonylureas or other oral hypoglycemic agents without appropriate glucose monitoring.

Use with caution

  • Diuretics that may alter sodium and potassium levels.
  • Beta‑blockers, which can mask hypoglycemia symptoms.
  • Corticosteroids or catecholamines that raise blood glucose.
  • Potassium‑containing solutions, due to potential shifts in serum potassium.
  • Other intravenous carbohydrate solutions, to prevent excessive caloric load.

Frequently Asked Questions

The only active ingredient in Glucose Proamp is glucose, a simple carbohydrate used to provide energy when administered intravenously.

Glucose Proamp is commonly used to treat hypoglycemia, as part of parenteral nutrition, for fluid replacement, and to provide intra‑operative glucose support.

Blood glucose should be measured before starting the infusion, periodically during the infusion, and after completion to ensure levels remain within the target range.

Safety data for use during pregnancy are limited; therefore, it should be used only if the potential benefit justifies the potential risk and under close medical supervision.

Common local reactions include mild irritation, redness, or phlebitis at the catheter insertion site.

Serious events may include severe hyperglycemia, anaphylaxis, cardiac arrhythmias, and hyperosmolar hyperglycemic state, particularly in patients with underlying metabolic disorders.

Concurrent high‑dose insulin can cause profound hypoglycemia; therefore, insulin dosing should be adjusted and glucose levels closely monitored when both are used.

In children, the infusion rate and total glucose load should be individualized based on weight and metabolic needs, with frequent glucose monitoring.

Rapid infusion may cause shifts in sodium and potassium levels; monitoring electrolytes is recommended, especially in patients with renal or cardiac disease.

The regulatory status varies by country; in the European Union, it is typically available by prescription or under medical supervision.

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

Mixing should be avoided unless compatibility has been confirmed, as interactions may affect the stability of the glucose solution or the co‑administered drug.

Published by

GNH India Pharmaceuticals Limited

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Last updated:

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