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Glucose Viaflo Baxter

Active Ingredient:
Glucose Monohydrate
Origin:
EU

Glucose Viaflo Baxter (Glucose Monohydrate)

Glucose Viaflo Baxter is an intravenous solution containing glucose monohydrate as the active ingredient. It is supplied in a sterile liquid form for parenteral administration, typically used in clinical settings for energy provision and fluid balance. The product is marketed in the European Union and requires a prescription. It is packaged in single‑use containers and is intended for use under the supervision of qualified health‑care professionals.

Manufacturer / TM Owner

Baxter Sa

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Indications & Clinical Uses

Glucose Viaflo Baxter is indicated for several clinical situations where rapid glucose delivery and fluid replacement are required.

  • Treatment of hypoglycemia when oral intake is not feasible.
  • Component of parenteral nutrition regimens to supply carbohydrate calories.
  • Fluid and electrolyte replacement in patients unable to tolerate oral fluids.
  • Support of plasma osmolarity during intravenous therapy.
  • Adjunct in perioperative care to maintain blood glucose levels.

Side Effects

Intravenous glucose monohydrate can elicit a spectrum of effects that reflect its role as a rapid energy source and its influence on plasma osmolarity. Most reactions are mild and reversible, while rare events may require medical attention.

Common

  • A temporary increase in blood glucose concentration that usually normalizes without intervention.
  • Mild gastrointestinal discomfort such as nausea or occasional vomiting shortly after infusion.
  • Localized irritation or erythema at the catheter insertion site.

Serious

  • Marked hyperglycemia that can progress to osmotic diuresis and dehydration.
  • Fluid overload manifesting as pulmonary edema, especially in patients with compromised cardiac function.
  • Immediate hypersensitivity reactions, including rash, bronchospasm, or anaphylactic shock.

Precautions & Warnings

When using Glucose Viaflo Baxter, clinicians should observe several precautionary measures to minimize risks and ensure appropriate patient monitoring.

  • Verify blood glucose level before administration to avoid excessive hyperglycemia.
  • Adjust infusion rate in patients with renal or cardiac insufficiency to prevent fluid overload.
  • Monitor electrolytes, particularly potassium and sodium, during and after infusion.
  • Use aseptic technique to reduce risk of catheter‑related infection.
  • Assess for signs of allergic reaction during the first minutes of infusion.
  • Consider alternative carbohydrate sources in patients with known glucose intolerance.

Avoid Interactions

Glucose Viaflo Baxter may interact with other medications or clinical conditions, influencing its safety and efficacy.

Avoid

  • Co‑administration with high‑dose insulin without glucose monitoring, which can precipitate severe hypoglycemia.
  • Simultaneous infusion of hypertonic dextrose solutions, increasing risk of hyperosmolar complications.
  • Use in patients with uncontrolled diabetes mellitus when glucose levels are already elevated.

Use with caution

  • Concurrent diuretics or potassium‑sparing agents that affect electrolyte balance.
  • Medications that prolong QT interval, as rapid glucose shifts may influence cardiac electrophysiology.
  • Renal replacement therapy, requiring adjustment of glucose infusion rates.

Frequently Asked Questions

The active ingredient is glucose monohydrate, a simple sugar used to provide energy in intravenous form.

It is commonly prescribed for hypoglycemia, as part of parenteral nutrition, and for fluid and electrolyte replacement when oral intake is not possible.

The product is supplied as a sterile intravenous solution and is administered directly into a vein by a healthcare professional.

No, Glucose Viaflo Baxter is a prescription‑only medication and must be ordered by a qualified prescriber.

Use in children should be determined by a physician, taking into account the specific clinical situation and dosing requirements.

Blood glucose levels, electrolytes, and fluid balance should be monitored regularly to detect any abnormal changes.

Common side effects include a temporary rise in blood glucose, mild nausea or vomiting, and local irritation at the infusion site.

Serious reactions can include severe hyperglycemia with osmotic diuresis, fluid overload leading to pulmonary edema, and allergic reactions such as anaphylaxis.

It should be used with caution in diabetic patients, and blood glucose should be closely monitored to avoid excessive hyperglycemia.

Interactions may occur with high‑dose insulin, other hypertonic dextrose solutions, and medications affecting electrolyte balance or cardiac conduction.

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

Mixing with other intravenous solutions should be done only under medical supervision to avoid incompatibility or osmolarity issues.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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