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Glucose Bp B. Braun Melsungen

Active Ingredient:
Glucose Monohydrate
Origin:
EU

Glucose Bp B. Braun Melsungen (Glucose Monohydrate)

Glucose Bp B. Braun Melsungen is an injectable solution containing glucose monohydrate as the sole active ingredient. It is supplied as a sterile aqueous solution for intravenous administration, with the specific concentration not disclosed in the product label. Marketed in the European Union and available by prescription only, this carbohydrate solution is used as an energy source and fluid component in clinical settings such as parenteral nutrition and hypoglycemia treatment.

Manufacturer / TM Owner

B.Braun Melsungen Ag

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Indications & Clinical Uses

Glucose Bp B. Braun Melsungen is employed in several clinical situations where rapid glucose supplementation or fluid replacement is required.

  • Treatment of acute hypoglycemia to quickly raise plasma glucose levels.
  • Component of parenteral nutrition regimens for patients unable to receive enteral feeding.
  • Fluid and electrolyte replacement in perioperative or trauma care.
  • Support of carbohydrate needs during prolonged fasting or critical illness.
  • Dilution medium for certain intravenous drug preparations.

Side Effects

Intravenous administration of glucose monohydrate may be associated with a range of physiological responses, most of which are predictable and dose‑related.

Common

  • Transient hyperglycemia with elevated blood glucose measurements.
  • Mild nausea or abdominal discomfort.
  • Local irritation or redness at the infusion site.
  • Electrolyte shifts, particularly decreased serum potassium.
  • Fluid overload in patients with compromised cardiac function.
  • Headache or dizziness due to rapid osmotic changes.

Serious

  • Severe hyperglycemia leading to osmotic diuresis.
  • Hypersensitivity reactions such as rash, urticaria, or anaphylaxis.
  • Hyperosmolar hyperglycemic state in susceptible patients.
  • Metabolic acidosis associated with extreme hyperglycemia.

Precautions & Warnings

When using Glucose Bp B. Braun Melsungen, clinicians should evaluate patient-specific factors and monitor relevant parameters to minimize risks.

  • Assess baseline blood glucose and adjust infusion rate accordingly.
  • Use caution in patients with diabetes mellitus or impaired glucose tolerance.
  • Monitor fluid balance in individuals with heart failure or renal insufficiency.
  • Check serum electrolytes, especially potassium and sodium, before and during therapy.
  • Avoid rapid infusion in neonates and low‑birth‑weight infants.
  • Consider compatibility with other intravenous solutions to prevent precipitation.
  • Discontinue if signs of hypersensitivity or severe hyperglycemia develop.

Avoid Interactions

Glucose monohydrate can interact with other medications or solutions administered intravenously, influencing efficacy or safety.

Avoid

  • Co‑administration with high‑dose insulin without appropriate glucose monitoring.
  • Mixing with calcium‑containing solutions that may precipitate.
  • Concurrent use of diuretics that exacerbate electrolyte disturbances.

Use with caution

  • Concurrent administration of potassium‑sparing agents; monitor serum potassium.
  • Use alongside beta‑blockers in diabetic patients, as they may mask hypoglycemia symptoms.
  • Combination with other hyperosmolar solutions; observe for fluid overload.

Frequently Asked Questions

It is primarily indicated for the rapid correction of hypoglycemia, as a component of parenteral nutrition, and for fluid and electrolyte replacement in clinical settings.

The product is supplied as a sterile aqueous solution that is infused directly into a vein using an appropriate IV set, with the infusion rate adjusted to the patient’s clinical needs.

Blood glucose levels, serum electrolytes, fluid balance, and signs of hypersensitivity should be monitored regularly throughout the infusion.

It may be used in children, including neonates, but infusion rates and concentrations should be carefully adjusted and monitored by a pediatric specialist.

Common side effects include transient hyperglycemia, mild nausea, local irritation at the infusion site, electrolyte shifts, fluid overload, and occasional headache or dizziness.

The intravenous formulation bypasses gastrointestinal absorption, providing immediate elevation of plasma glucose and allowing precise control of fluid volume, which is not possible with oral solutions.

Compatibility depends on the specific medication; it is generally compatible with many solutions but may precipitate when mixed with calcium‑containing or highly acidic drugs.

Patients with renal dysfunction should have their fluid status and electrolyte levels closely monitored, and infusion rates may need to be reduced to avoid fluid overload.

It supplies a readily available source of carbohydrate calories, helping to meet the energy requirements of patients who cannot receive enteral nutrition.

The infusion should be stopped immediately, and appropriate medical treatment for the allergic reaction, such as antihistamines or epinephrine, should be administered.

Yes, but the glucose infusion rate must be coordinated with insulin dosing and blood glucose monitoring to avoid severe hyperglycemia or hypoglycemia.

A specific maximum dose is not defined in the product label; dosing should be individualized based on the patient’s metabolic needs, blood glucose levels, and overall fluid balance.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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