Product image of Glucos Viaflo Baxter (Glucose) supplied by GNH India

Glucos Viaflo Baxter

Active Ingredient:
Glucose
Origin:
EU

Glucos Viaflo Baxter (Glucose)

Glucos Viaflo Baxter is an injectable solution containing glucose as the sole active ingredient, supplied in a sterile aqueous formulation for intravenous administration. The product is marketed in the European Union and is prescribed as a parenteral source of carbohydrate when oral intake is insufficient or when rapid correction of low blood glucose is required. It is provided without a specified concentration on the label.

Manufacturer / TM Owner

Baxter Medical Ab

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Indications & Clinical Uses

Glucos Viaflo Baxter is used in clinical settings to supply carbohydrate energy and maintain fluid balance when oral nutrition is not feasible.

  • Treatment of hypoglycemia in patients unable to take oral glucose.
  • Component of total parenteral nutrition regimens for patients requiring intravenous carbohydrate support.
  • Fluid replacement in conjunction with electrolytes for dehydration or surgical patients.
  • Support during perioperative fasting to prevent energy deficit.
  • Adjunct in neonatal intensive care for infants with low blood glucose.
  • Used for electrolyte‑balanced rehydration in patients with gastrointestinal losses.

Side Effects

Glucos Viaflo Baxter may be associated with infusion‑related reactions and metabolic changes, which are typically categorized by frequency and severity.

Common

  • Transient hyperglycemia or elevated blood glucose levels, usually resolving after infusion cessation.
  • Mild infusion site irritation or erythema, typically transient.
  • Nausea or mild abdominal discomfort.
  • Headache or dizziness during rapid infusion.
  • Temporary increase in serum osmolality.
  • Mild metabolic acidosis in patients with renal impairment.

Serious

  • Severe hyperglycemia leading to osmotic diuresis, may require insulin therapy.
  • Hypotension from rapid fluid administration.
  • Electrolyte imbalance, particularly hyponatremia.
  • Allergic reaction such as urticaria or anaphylaxis.
  • Volume overload leading to pulmonary edema in patients with cardiac dysfunction.

Precautions & Warnings

When prescribing Glucos Viaflo Baxter, clinicians should assess patient-specific factors and monitor for potential complications related to glucose infusion and fluid volume.

  • Verify baseline blood glucose and adjust infusion rate to avoid hyperglycemia.
  • Assess renal and hepatic function before administration, as clearance may be altered.
  • Evaluate cardiac status to prevent volume overload in patients with heart failure.
  • Use caution in pregnant or lactating women; limited safety data are available.
  • Monitor electrolytes, especially sodium and potassium, during prolonged therapy.
  • Ensure aseptic technique to reduce risk of catheter‑related infection.

Avoid Interactions

Glucos Viaflo Baxter can interact with other agents that affect blood glucose, fluid balance, or electrolyte status, requiring careful coordination with concurrent therapies.

Avoid

  • Co‑administration with high‑dose insulin without glucose monitoring, due to risk of severe hypoglycemia.
  • Rapid infusion together with other hypertonic solutions, which may cause abrupt osmotic shifts.
  • Concurrent administration with other glucose‑containing solutions, which may lead to excessive caloric load.

Use with caution

  • Concurrent use of diuretics that may exacerbate electrolyte disturbances.
  • Patients receiving total parenteral nutrition containing other carbohydrate sources; monitor total glucose load.
  • Anticoagulants, as large fluid volumes can dilute plasma concentrations.
  • Beta‑blockers, because they may mask symptoms of hypoglycemia.

Frequently Asked Questions

Glucos Viaflo Baxter is primarily indicated for the treatment of hypoglycemia and as a carbohydrate component of parenteral nutrition when oral intake is not possible.

The product is supplied as a sterile solution for intravenous injection and is administered through a controlled infusion set according to the prescribed rate.

It may be used in pediatric settings, especially in neonatal intensive care, but dosing and monitoring should be individualized by a qualified healthcare professional.

Blood glucose levels, electrolytes, and fluid balance should be regularly monitored to detect hyperglycemia, electrolyte shifts, or volume overload.

Compatibility should be assessed on a case‑by‑case basis; avoid mixing with other hypertonic glucose solutions to prevent excessive caloric load.

Common side effects include transient hyperglycemia, mild infusion site irritation, nausea, headache, and temporary changes in serum osmolality.

Serious reactions may involve severe hyperglycemia, hypotension, electrolyte imbalance, allergic reactions such as anaphylaxis, and volume overload leading to pulmonary edema.

Insulin dosing may need adjustment to prevent hypoglycemia; coordination with glucose monitoring is essential.

Safety data in pregnancy are limited; it should be used only if the potential benefit justifies the potential risk to the fetus.

Store the solution in a controlled room temperature environment, protected from light, and follow the manufacturer’s stability guidelines.

It can contribute to fluid replacement, but electrolytes may need to be added separately to meet the patient’s specific needs.

The product is classified under ATC code B05BB01, indicating it is a glucose solution used as an excipient or solvent.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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