Product image of Glucose Sterile Concentrate B. Braun Medical (Glucose, Anhydrous) supplied by GNH India

Glucose Sterile Concentrate B. Braun Medical

Active Ingredient:
Glucose, Anhydrous
Origin:
EU

Glucose Sterile Concentrate B. Braun Medical (Glucose, Anhydrous)

Glucose Sterile Concentrate B. Braun Medical is a sterile aqueous solution containing anhydrous glucose as the sole active ingredient. It is supplied as an intravenous (IV) solution without a specified concentration, intended for parenteral administration in clinical settings. The product is classified as an excipient/carbohydrate solution and is marketed in the European Union for use under prescription. It supports energy metabolism during intravenous therapy in hospitalized patients.

Manufacturer / TM Owner

B. Braun Medical Ltd.

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Indications & Clinical Uses

Glucose Sterile Concentrate is indicated for several clinical situations where rapid intravenous glucose delivery is required.

  • Carbohydrate source in total or supplemental parenteral nutrition formulations.
  • Treatment of documented hypoglycemia when oral glucose is not feasible.
  • Component of fluid and electrolyte replacement solutions that provide caloric support.
  • Maintenance of blood glucose levels during intraoperative or postoperative care.
  • Dilution medium for certain intravenous medications that require a glucose carrier.

Side Effects

When administered intravenously, glucose solutions may be associated with predictable physiological responses and, rarely, more serious complications.

Common

  • Transient hyperglycemia.
  • Local irritation at the infusion site.
  • Mild electrolyte shifts, such as changes in sodium or potassium levels.

Serious

  • Severe hyperglycemia leading to osmotic diuresis.
  • Hypoglycemia after abrupt discontinuation of the infusion.
  • Fluid overload or pulmonary edema in patients with compromised cardiac or renal function.
  • Allergic or anaphylactic reaction to the solution components.

Precautions & Warnings

Clinicians should evaluate patient-specific factors and monitor parameters to minimize risks associated with intravenous glucose administration.

  • Assess baseline blood glucose and adjust infusion rate accordingly.
  • Monitor for signs of fluid overload, especially in patients with cardiac or renal impairment.
  • Use caution in patients with uncontrolled diabetes mellitus or insulin resistance.
  • Verify compatibility with other IV drugs before co‑administration.
  • Avoid rapid infusion rates that exceed recommended osmolarity limits.
  • Consider electrolyte status, particularly potassium and phosphate, before initiating therapy.

Avoid Interactions

Glucose Sterile Concentrate can interact with other intravenous agents, affecting stability or metabolic outcomes.

Avoid

  • Co‑administration with high‑dose insulin infusions without appropriate glucose monitoring.
  • Mixing with calcium‑containing solutions that may precipitate.
  • Concurrent use of drugs that cause hyperglycemia (e.g., corticosteroids) without dose adjustment.

Use with caution

  • Concurrent administration of potassium chloride solutions, as glucose can drive potassium into cells.
  • Use alongside diuretics that alter fluid balance, requiring close monitoring.
  • Combination with other carbohydrate‑containing fluids, which may increase total caloric load.

Frequently Asked Questions

It is used as an intravenous source of glucose for parenteral nutrition, treatment of hypoglycemia, and as part of fluid and electrolyte replacement regimens.

Yes, the product is classified as prescription‑only (Rx) and must be ordered by a qualified healthcare professional.

Compatibility should be confirmed before mixing; some drugs, especially calcium‑containing solutions, may precipitate when combined with glucose solutions.

The anhydrous glucose provides an immediate source of energy that cells can metabolize via glycolysis and subsequent oxidative pathways.

Blood glucose levels, fluid balance, electrolytes, and signs of overload should be regularly assessed throughout the infusion.

It can be used in diabetic patients, but infusion rates must be carefully titrated and glucose levels closely monitored.

Common effects include transient hyperglycemia, mild local irritation at the infusion site, and modest shifts in electrolyte concentrations.

Serious events may include severe hyperglycemia, fluid overload leading to pulmonary edema, hypoglycemia after abrupt discontinuation, and rare allergic reactions.

Use in children is possible under medical supervision, with dosing and infusion rates adjusted to pediatric physiological needs.

The product is classified under ATC code B05BA01, which corresponds to carbohydrate solutions for parenteral nutrition.

It should be stored according to the manufacturer’s instructions, typically at controlled room temperature and protected from light.

The solution is supplied sterile; however, aseptic technique must be maintained during preparation and administration to prevent contamination.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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