Product image of Glucoza Infomed Fluids (Glucose Monohydrate) supplied by GNH India

Glucoza Infomed Fluids

Active Ingredient:
Glucose Monohydrate
Origin:
EU

Glucoza Infomed Fluids (Glucose Monohydrate)

Glucoza Infomed Fluids is an intravenous solution that contains glucose monohydrate as the active ingredient. The product is supplied in a standard strength (strength not specified) and is manufactured for the European Union market. It is classified as an excipient and is used primarily as a source of carbohydrate in clinical settings. The solution is sterile, isotonic, and intended for administration by healthcare professionals in hospitals, clinics, or emergency care environments.

Manufacturer / TM Owner

Infomed Fluids Srl

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Indications & Clinical Uses

Glucoza Infomed Fluids is employed in a variety of clinical situations where rapid carbohydrate supplementation is required, particularly in acute care settings.

  • Management of hypoglycemia when oral glucose is not feasible.
  • Provision of caloric support during peri‑operative fasting.
  • Fluid replacement in patients with dehydration and low blood glucose.
  • Dilution and carrier for intravenous medications that require a glucose base.
  • Support for metabolic demands in critically ill or trauma patients.

Side Effects

When administered intravenously, glucose monohydrate solutions can produce a range of physiological responses, most of which are related to changes in blood glucose and fluid balance.

Common

  • Transient increase in blood glucose levels.
  • Mild hyperosmolarity leading to temporary thirst.
  • Local irritation at the infusion site.
  • Nausea or mild abdominal discomfort.
  • Headache or dizziness during infusion.

Serious

  • Severe hyperglycemia requiring medical intervention.
  • Fluid overload causing pulmonary edema.
  • Electrolyte imbalance, particularly hyponatremia.
  • Allergic reaction such as rash, itching, or anaphylaxis.

Precautions & Warnings

Healthcare providers should observe several precautionary measures before and during the administration of Glucoza Infomed Fluids to ensure patient safety and optimal therapeutic effect.

  • Verify patient’s blood glucose level and adjust infusion rate accordingly.
  • Assess fluid status to avoid volume overload, especially in cardiac or renal impairment.
  • Use aseptic technique to prevent catheter‑related infections.
  • Monitor electrolytes, particularly sodium and potassium, during prolonged therapy.
  • Avoid rapid infusion in neonates or patients with compromised circulation.
  • Discontinue if signs of allergic reaction or severe hyperglycemia develop.

Avoid Interactions

Glucose monohydrate solutions may interact with other intravenous agents or patient conditions, influencing efficacy or safety.

Avoid

  • Co‑administration with high‑dose insulin infusions without close glucose monitoring.
  • Simultaneous infusion of hypertonic saline solutions that could exacerbate hyperosmolar states.
  • Use in patients with known severe glucose intolerance or uncontrolled diabetes without specialist oversight.

Use with caution

  • Concurrent administration of diuretics, which may alter fluid and electrolyte balance.
  • Infusion alongside catecholamines, as they can affect glucose metabolism.
  • Patients receiving total parenteral nutrition, requiring careful monitoring of total carbohydrate load.

Frequently Asked Questions

The active ingredient is glucose monohydrate, a simple carbohydrate used for intravenous supplementation.

It is used for rapid correction of hypoglycemia, peri‑operative caloric support, fluid replacement with glucose, and as a carrier for other IV medications.

The solution should be stored in a cool, dry place, protected from light, and kept within the temperature range specified on the packaging.

Yes, but dosing and infusion rates must be adjusted for age, weight, and clinical condition under medical supervision.

Common effects include a temporary rise in blood glucose, mild thirst, local irritation at the infusion site, nausea, and occasional headache.

Severe hyperglycemia, fluid overload leading to pulmonary edema, electrolyte disturbances such as hyponatremia, and allergic reactions like rash or anaphylaxis should be reported promptly.

It can be used as a diluent for compatible medications, but compatibility should be verified according to manufacturer guidelines.

Yes, concurrent high‑dose insulin may cause rapid changes in blood glucose; close monitoring is essential.

Regular checks of blood glucose, fluid balance, and electrolytes are recommended, especially during prolonged administration.

Use with caution; assess fluid status and avoid volume overload in patients with compromised renal function.

The product is generally classified as prescription‑only and should be administered by qualified healthcare professionals.

The exact concentration is not specified on the label; clinicians should refer to the product insert for detailed formulation information.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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