Product image of Glucosio Bioindustria L.I.M. (Glucose Monohydrate) supplied by GNH India

Glucosio Bioindustria L.I.M.

Active Ingredient:
Glucose Monohydrate
Origin:
EU

Glucosio Bioindustria L.I.M. (Glucose Monohydrate)

Glucosio Bioindustria L.I.M. is an intravenous preparation whose active ingredient is glucose monohydrate. It is supplied as a sterile solution intended for parenteral use in the European market. The product functions as an excipient and source of carbohydrate energy in clinical settings, providing a readily available form of glucose for patients requiring intravenous supplementation.

Manufacturer / TM Owner

Bioindustria Lim Laboratorio Italiano Medicinali Spa

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Indications & Clinical Uses

Glucosio Bioindustria L.I.M. is employed in medical practice primarily as a source of carbohydrate energy and as a diluent for intravenous drug preparations. It may be used in the following contexts:

  • Intravenous fluid therapy to maintain blood glucose levels during fasting or surgery.
  • As a carrier solution for the reconstitution of injectable medications.
  • In pediatric and neonatal care where rapid glucose delivery is needed.
  • For metabolic testing and diagnostic procedures requiring controlled glucose infusion.
  • In emergency medicine to treat hypoglycemia when oral intake is not possible.

Side Effects

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

Common

  • Mild hyperglycemia that resolves without intervention.
  • Transient nausea or vomiting during infusion.
  • Local irritation or erythema at the infusion site.
  • Mild electrolyte shifts, such as slight potassium changes.
  • Headache or dizziness related to rapid glucose administration.

Serious

  • Severe hyperglycemia leading to osmotic diuresis.
  • Hyperosmolar hyperglycemic state in susceptible individuals.
  • Allergic or anaphylactoid reactions presenting as rash or respiratory distress.
  • Fluid overload causing pulmonary edema.
  • Significant electrolyte imbalance requiring medical management.

Precautions & Warnings

When using Glucosio Bioindustria L.I.M., clinicians should observe several safety considerations to minimize risk. Important precautions include:

  • Assess baseline blood glucose and monitor levels during and after infusion.
  • Adjust infusion rate in patients with renal or cardiac insufficiency to avoid fluid overload.
  • Use caution in individuals with known glucose metabolism disorders, such as diabetes mellitus.
  • Verify compatibility with other intravenous medications before mixing.
  • Store the solution according to manufacturer guidelines to maintain sterility.
  • Document any adverse reactions promptly in the patient record.

Avoid Interactions

Glucose monohydrate solutions can interact with other agents administered intravenously. Awareness of these interactions helps ensure safe patient care.

Avoid

  • Co‑administration with high‑dose insulin without appropriate monitoring, which may precipitate severe hypoglycemia.
  • Mixing with calcium‑containing solutions that can precipitate calcium phosphate.
  • Concurrent infusion of potassium chloride in high concentrations, risking hyperkalemia.

Use with caution

  • Concurrent use of diuretics that may alter fluid and electrolyte balance.
  • Administration alongside beta‑blockers, which can mask signs of hypoglycemia.
  • Use with other hyperosmolar solutions, monitoring for osmotic shifts.
  • Combination with medications that affect renal function, requiring dose adjustments.

Frequently Asked Questions

The primary component is glucose monohydrate, a simple carbohydrate used for intravenous energy supplementation.

It is intended for intravenous (IV) administration as a sterile solution.

Yes, it can serve as a diluent for reconstituting certain injectable medications, provided compatibility is confirmed.

Blood glucose levels should be monitored before, during, and after infusion, along with observation for signs of fluid overload.

It may be used in pediatric and neonatal care when rapid glucose delivery is required, under appropriate medical supervision.

Common mild side effects include transient hyperglycemia, nausea, local infusion site irritation, mild electrolyte shifts, and headache.

Serious reactions can include severe hyperglycemia, hyperosmolar hyperglycemic state, allergic responses, fluid overload, and significant electrolyte imbalances.

Mixing with calcium‑containing solutions should be avoided because it may cause precipitation of calcium phosphate.

Store according to the manufacturer’s instructions, typically in a cool, dry place away from direct sunlight, and keep the container sealed until use.

Patients with diabetes require careful blood glucose monitoring and possible adjustment of insulin therapy when receiving the solution.

Yes, especially in patients with cardiac or renal impairment; infusion rates should be adjusted accordingly.

The product is manufactured for the European Union (EU) market.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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