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 a pharmaceutical product that contains glucose as its active ingredient, supplied as an intravenous solution for injection. The exact concentration or strength is not specified in the available documentation. Marketed in the European Union, this sterile solution is classified as an excipient used primarily in parenteral nutrition formulations to provide a source of carbohydrate energy. It is intended for use under professional medical supervision.

Manufacturer / TM Owner

Baxter Medical Ab

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Indications & Clinical Uses

Glucos Viaflo Baxter is employed in clinical settings as part of parenteral nutrition regimens to supply carbohydrate calories.

  • Provides an immediate source of glucose for patients unable to receive enteral feeding.
  • Supports energy metabolism during surgical procedures or critical illness.
  • Used to maintain blood glucose levels in patients receiving total parenteral nutrition.
  • Assists in preventing hypoglycemia in neonatal and pediatric intensive care.
  • Facilitates formulation of customized nutrition admixtures for adult patients.
  • Can be combined with amino acid and lipid solutions to create balanced total nutrient admixtures.
  • Provides flexibility in adjusting carbohydrate concentration to meet individual caloric requirements.

Side Effects

Glucos Viaflo Baxter, as an intravenous glucose solution, may be associated with certain adverse reactions that vary in frequency and severity.

Common

  • Transient hyperglycemia or elevated blood glucose levels.
  • Local irritation or pain at the injection site.
  • Mild electrolyte disturbances, such as low potassium.
  • Nausea or vomiting in some patients.
  • Mild headache or dizziness reported occasionally.
  • Temporary increase in serum triglyceride levels.

Serious

  • Severe hyperglycemia leading to osmotic diuresis.
  • Allergic reactions, including rash, itching, or anaphylaxis.
  • Fluid overload or pulmonary edema in patients with compromised cardiac function.
  • Severe electrolyte imbalance, such as hypernatremia, requiring medical intervention.
  • Monitoring of blood parameters is recommended during administration.

Precautions & Warnings

When using Glucos Viaflo Baxter, healthcare professionals should observe specific precautions to ensure patient safety and optimal therapeutic outcomes.

  • Verify patient’s blood glucose level before infusion to avoid excessive hyperglycemia.
  • Assess renal and hepatic function, as impaired clearance may affect glucose metabolism.
  • Adjust infusion rate in patients with cardiac failure to prevent fluid overload.
  • Use aseptic technique to maintain sterility of the intravenous solution.
  • Monitor electrolytes, especially potassium and sodium, during prolonged administration.
  • Consider contraindications such as known hypersensitivity to glucose solutions.

Avoid Interactions

Glucos Viaflo Baxter may interact with other intravenous therapies or medications; awareness of potential interactions helps prevent complications.

Avoid

  • Co-administration with high‑dose insulin infusions without glucose monitoring, which can cause severe hypoglycemia.
  • Simultaneous infusion of hypertonic saline solutions that may exacerbate hypernatremia.

Use with caution

  • Concurrent use of diuretics, which can alter electrolyte balance during glucose infusion.
  • Administration alongside catecholamines (e.g., epinephrine) that may increase glucose production and affect glycemic control.
  • Overlapping infusion with lipid emulsions, requiring careful monitoring of caloric load.
  • Use with potassium‑sparing agents, as glucose infusion can shift potassium intracellularly.

Frequently Asked Questions

Glucos Viaflo Baxter is an intravenous solution that contains glucose as the sole active ingredient. It is supplied as a sterile, aqueous solution for injection, intended for use as an excipient in parenteral nutrition.

The solution is added to total parenteral nutrition admixtures to provide a source of carbohydrate calories, helping to meet the energy requirements of patients who cannot receive enteral feeding.

Patients in intensive care, postoperative settings, or those with gastrointestinal dysfunction who require total parenteral nutrition may receive the product.

Common adverse effects include transient hyperglycemia, local irritation at the injection site, mild electrolyte disturbances such as low potassium, nausea, vomiting, mild headache, and temporary increases in triglyceride levels.

Blood glucose levels should be measured before starting the infusion and periodically during therapy to detect and manage any rise in glucose concentrations.

Known hypersensitivity to glucose solutions is a contraindication. Caution is advised in patients with severe hyperglycemia, uncontrolled diabetes, or conditions predisposing to fluid overload.

The product should be stored in a cool, dry place protected from light, and kept within the temperature range specified on the label until the expiration date.

It can be combined with compatible amino acid, lipid, and electrolyte solutions to create a complete parenteral nutrition admixture, but compatibility with each specific medication should be verified.

Renal function should be assessed, and glucose infusion rates may need adjustment because impaired kidneys can affect glucose handling and electrolyte balance.

When insulin is administered concurrently, glucose monitoring is essential to avoid severe hypoglycemia; insulin doses may need to be adjusted based on the amount of glucose infused.

Infusion rates should be individualized based on the patient’s caloric needs, blood glucose targets, and overall fluid balance, and determined by the prescribing clinician.

Yes, the product is marketed within the European Union and complies with the regulatory requirements applicable to intravenous glucose solutions.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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