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Glucose Lavoisier

Active Ingredient:
Glucose
Origin:
EU

Glucose Lavoisier (Glucose)

Glucose Lavoisier is an intravenous solution containing glucose as the active ingredient. It is supplied as a sterile solution for injection, marketed in the European Union. The product provides a readily available source of carbohydrate energy and is used in clinical settings for parenteral nutrition, treatment of hypoglycemia, and fluid and electrolyte replacement. Formulation strength is not specified in the available data, currently publicly disclosed by the manufacturer.

Manufacturer / TM Owner

Laboratoires Chaix Et Du Marais

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Indications & Clinical Uses

Glucose Lavoisier is indicated for clinical situations where rapid carbohydrate supplementation or fluid replacement is required, particularly in hospital or intensive‑care environments. It may be administered intravenously as part of a broader therapeutic regimen.

  • Management of acute hypoglycemia when oral glucose is not feasible.
  • Component of parenteral nutrition formulas for patients unable to eat orally.
  • Support of fluid and electrolyte balance during peri‑operative care.
  • Treatment of dehydration combined with carbohydrate loss in critical illness.
  • Adjunct in metabolic testing or glucose tolerance assessments under medical supervision.

Side Effects

Intravenous administration of Glucose Lavoisier can produce a spectrum of physiological responses, most of which are directly related to the rapid increase in plasma glucose and the osmotic load of the solution, and are generally predictable in clinical practice.

Common

  • Transient elevation of blood glucose levels, typically observed within minutes of infusion and returning to baseline after cessation.
  • Mild gastrointestinal discomfort such as nausea or occasional vomiting, especially with rapid infusion rates.
  • Local irritation or erythema at the catheter insertion site, which usually resolves without intervention.

Serious

  • Significant hyperglycemia that may require insulin therapy or adjustment of the glucose infusion rate.
  • Fluid overload leading to pulmonary edema, particularly in patients with compromised cardiac or renal function.
  • Electrolyte disturbances, including hyponatremia or hypokalemia, resulting from shifts associated with glucose metabolism.

Precautions & Warnings

Prior to using Glucose Lavoisier, clinicians should evaluate patient-specific factors and monitor relevant parameters to minimize risks associated with intravenous carbohydrate administration.

  • Assess baseline blood glucose and adjust infusion rate in diabetic patients.
  • Monitor fluid balance to avoid overload, especially in patients with cardiac or renal impairment.
  • Check serum electrolytes before and during therapy to detect shifts.
  • Use aseptic technique to prevent catheter‑related infections.
  • Avoid rapid infusion in neonates or patients with compromised vascular integrity.
  • Review compatibility with other intravenous solutions to prevent precipitation.

Avoid Interactions

Glucose Lavoisier may interact with other medications or solutions administered intravenously, influencing glucose metabolism or solution stability.

Avoid

  • Co‑administration with insulin infusions without appropriate dose adjustment.
  • Mixing with calcium‑containing solutions that can cause precipitation.

Use with caution

  • Concurrent use of glucocorticoids, which may exacerbate hyperglycemia.
  • Administration alongside diuretics that affect fluid balance.
  • Use with beta‑adrenergic agonists that can increase glucose production.

Frequently Asked Questions

Glucose Lavoisier is a sterile glucose solution for injection that is administered intravenously to provide carbohydrate energy and fluid replacement.

It is commonly used for treating acute hypoglycemia, as part of parenteral nutrition, and for fluid and electrolyte replacement in hospitalized patients.

Yes, but clinicians must monitor blood glucose closely and adjust the infusion rate to avoid hyperglycemia.

Common effects include a temporary rise in blood glucose, mild nausea or vomiting, and possible local irritation at the injection site.

Serious events include significant hyperglycemia, fluid overload leading to pulmonary edema, and electrolyte disturbances such as hyponatremia or hypokalemia.

Fluid input and output should be regularly measured, especially in patients with cardiac or renal disease, to prevent overload.

Compatibility should be checked; it should not be mixed with calcium‑containing solutions because precipitation can occur.

Insulin may be required, but dosage must be carefully adjusted to avoid severe hypoglycemia or hyperglycemia.

Baseline and periodic measurements of blood glucose, serum electrolytes, and renal function are recommended.

It can be used with caution; infusion rates should be reduced and close monitoring is essential.

The solution should be stored according to the manufacturer’s instructions, typically at controlled room temperature and protected from light.

The regulatory status varies by country; in the EU it is generally prescribed by a healthcare professional.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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