Product image of Glucose B.Braun (Glucose Monohydrate) supplied by GNH India

Glucose B.Braun

Active Ingredient:
Glucose Monohydrate
Origin:
EU

Glucose B.Braun (Glucose Monohydrate)

Glucose B.Braun is an intravenous solution containing the active ingredient glucose monohydrate. It is supplied in a sterile liquid form intended for parenteral administration. The product conforms to European Union pharmaceutical standards and is classified as an excipient rather than a therapeutic drug. Glucose B.Braun provides a readily available source of glucose for cellular energy metabolism when infused into the bloodstream of patients during treatment.

Manufacturer / TM Owner

B.Braun Medical Sas

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Indications & Clinical Uses

Glucose B.Braun is used primarily to restore or maintain blood glucose concentrations in clinical settings where oral intake is not feasible.

  • Provides rapid glucose supplementation during surgery or anesthesia.
  • Supports energy needs in patients receiving total parenteral nutrition.
  • Corrects hypoglycemia in emergency or critical‑care situations.
  • Serves as a carrier solution for compatible intravenous medications.
  • Assists in metabolic testing protocols that require controlled glucose infusion.

Side Effects

When administered intravenously, glucose monohydrate may be associated with a range of observed effects, most of which are related to its metabolic role.

Common

  • Transient hyperglycemia
  • Mild electrolyte shift (e.g., potassium)
  • Local irritation at the infusion site
  • Nausea or vomiting if infused rapidly

Serious

  • Severe hyperglycemia leading to osmotic diuresis
  • Hypersensitivity reactions such as rash or anaphylaxis
  • Fluid overload in patients with compromised cardiac function
  • Metabolic acidosis in cases of massive infusion

Precautions & Warnings

Clinicians should consider several precautionary measures before selecting Glucose B.Braun for intravenous therapy.

  • Verify patient’s baseline blood glucose and adjust infusion rate accordingly.
  • Assess renal and cardiac function to avoid fluid overload or electrolyte imbalance.
  • Use aseptic technique to prevent catheter‑related infections.
  • Avoid concurrent administration with high‑dose insulin without monitoring.
  • Monitor serum electrolytes, especially potassium and phosphate, during prolonged infusion.
  • Consider contraindication in patients with known hypersensitivity to glucose solutions.

Avoid Interactions

Glucose B.Braun can interact with other agents administered intravenously; awareness of these interactions helps maintain safety.

Avoid

  • High‑dose insulin boluses without glucose supplementation, which may precipitate severe hypoglycemia.
  • Hyperosmolar dextrose solutions combined with other hypertonic fluids, increasing risk of osmotic injury.
  • Medications that require a low‑glucose environment, such as certain chemotherapeutic agents, where excess glucose may reduce efficacy.

Use with caution

  • Diuretics that affect electrolyte balance, requiring close monitoring of potassium.
  • Calcium channel blockers, as rapid glucose infusion can influence hemodynamics.
  • Blood products, because glucose can affect the stability of some components.

Frequently Asked Questions

Glucose B.Braun is used to quickly raise or maintain blood glucose levels in patients who cannot take oral nutrition, such as during surgery, critical care, or total parenteral nutrition.

The product is supplied as a sterile intravenous solution and is infused directly into the bloodstream through a catheter or IV line under aseptic conditions.

Glucose B.Braun may be used in children when a healthcare professional determines the appropriate dose and monitors glucose levels closely; specific pediatric dosing guidelines should be consulted.

Regular monitoring of blood glucose, serum electrolytes (especially potassium and phosphate), and fluid balance is recommended to detect hyperglycemia, electrolyte shifts, or fluid overload.

Allergic reactions are rare but possible; signs may include rash, itching, swelling, or anaphylaxis, and infusion should be stopped immediately if such symptoms occur.

Glucose B.Braun delivers glucose directly into the bloodstream, providing a rapid rise in blood sugar, whereas oral tablets must be absorbed through the gastrointestinal tract, which is slower and may be unsuitable for patients unable to swallow.

The solution should be stored at controlled room temperature, protected from light, and kept in its original sealed container until use.

Compatibility depends on the specific medication; it is generally compatible with many IV drugs, but compatibility should be verified with the manufacturer’s guidelines before co‑administration.

The infusion rate should be reduced or paused, and insulin therapy may be considered under medical supervision while continuing to monitor glucose levels.

Glucose B.Braun is classified as an unscheduled excipient; its use typically requires a healthcare professional’s order, but it is not listed as a controlled prescription medication.

The product is a sterile glucose monohydrate solution without added preservatives; formulation details are provided on the product label.

Contraindications include known hypersensitivity to glucose solutions and situations where rapid glucose infusion could exacerbate fluid overload or severe hyperglycemia.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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