Product image of Glucose Viaflo Baxter Médico-Farmacêutica (Glucose) supplied by GNH India

Glucose Viaflo Baxter Médico-Farmacêutica

Active Ingredient:
Glucose
Origin:
EU

Glucose Viaflo Baxter Médico-Farmacêutica (Glucose)

Glucose Viaflo Baxter Médico-Farmacêutica is an intravenous solution for injection that contains glucose as the sole active ingredient. It is supplied in a sterile liquid form without a specified strength, and is marketed in the European Union. The product is classified as an excipient used in parenteral nutrition and fluid replacement, and it requires a prescription (Rx) for use. It is intended for administration by healthcare professionals in clinical settings.

Manufacturer / TM Owner

Baxter Médico-Farmacêutica, Lda.

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Indications & Clinical Uses

Glucose Viaflo Baxter Médico-Farmacêutica is used when rapid provision of carbohydrate energy is required, particularly in settings where oral intake is not possible or insufficient. It serves as a component of parenteral nutrition regimens and can be employed for immediate correction of low blood glucose levels.

  • Management of hypoglycemia in patients unable to take oral glucose.
  • Supplementation of carbohydrate calories in total parenteral nutrition formulations.
  • Fluid replacement therapy when combined with electrolytes and vitamins.
  • Support during perioperative periods to maintain plasma glucose stability.
  • Treatment of metabolic demands in critically ill or trauma patients.

Side Effects

Intravenous administration of glucose may be associated with a range of physiological responses, most of which are predictable and dose‑related.

Common

  • Transient hyperglycemia that resolves with metabolic clearance.
  • Mild irritation or pain at the injection site.
  • Electrolyte shifts, particularly decreased serum potassium.
  • Fluid overload in patients receiving large volumes.

Serious

  • Severe hyperglycemia leading to osmotic diuresis.
  • Hypoglycemia if glucose infusion is abruptly discontinued.
  • Allergic or anaphylactic reaction to the solution components.
  • Hyperosmolar hyperglycemic state in susceptible individuals.

Precautions & Warnings

Before initiating therapy with Glucose Viaflo Baxter Médico-Farmacêutica, clinicians should evaluate patient-specific factors and monitor relevant clinical parameters to minimize risks.

  • Assess baseline blood glucose and adjust infusion rate accordingly.
  • Monitor serum electrolytes, especially potassium and sodium, during treatment.
  • Use caution in patients with renal or cardiac insufficiency due to fluid volume concerns.
  • Avoid rapid infusion in neonates and infants to prevent metabolic disturbances.
  • Review concomitant insulin therapy to prevent extreme glucose fluctuations.
  • Ensure sterility; discard any solution that appears cloudy or discolored.

Avoid Interactions

Glucose solutions can interact with other intravenous agents or systemic medications, influencing glucose metabolism or fluid balance.

Avoid

  • Concurrent high‑dose insulin infusions without appropriate glucose supplementation.
  • Co‑administration with other hypertonic dextrose solutions, which may cause excessive osmolar load.
  • Simultaneous infusion of potassium chloride in concentrations that could precipitate in the line.

Use with caution

  • Patients receiving diuretics, as fluid shifts may affect glucose concentration.
  • Medications that affect renal glucose handling, such as SGLT2 inhibitors.
  • Catecholamine or glucocorticoid therapy, which can increase endogenous glucose production.

Frequently Asked Questions

The product is primarily indicated for the treatment of hypoglycemia, as part of parenteral nutrition, and for fluid replacement when administered intravenously.

It is supplied as a sterile solution for injection and is administered intravenously, typically through a peripheral or central venous line under medical supervision.

Use in neonates and infants requires careful dosing and monitoring to avoid rapid shifts in plasma glucose and osmolar balance; it should be prescribed by a pediatric specialist.

Blood glucose levels, serum electrolytes (especially potassium and sodium), and fluid balance should be regularly monitored throughout the infusion.

Yes, especially when large volumes are infused; clinicians should assess cardiac and renal function and adjust infusion rates accordingly.

The infusion should be stopped immediately, and appropriate medical treatment for an allergic or anaphylactic reaction should be initiated.

When insulin is administered concurrently, glucose infusion rates may need to be adjusted to prevent severe hypoglycemia or hyperglycemia.

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

Compatibility should be confirmed for each medication; avoid mixing with other hypertonic dextrose solutions or incompatible electrolytes without proper guidelines.

Contraindications include known hypersensitivity to the product components and conditions where rapid glucose administration could exacerbate metabolic disturbances, such as uncontrolled diabetes mellitus.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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