Product image of Glucose-Lösung Deltamedica (Glucose, Anhydrous) supplied by GNH India

Glucose-Lösung Deltamedica

Active Ingredient:
Glucose, Anhydrous
Origin:
EU

Glucose-Lösung Deltamedica (Glucose, Anhydrous)

Glucose-Lösung Deltamedica is an intravenous solution for injection that contains the active ingredient Glucose, Anhydrous. It is supplied as a sterile solution without a specified concentration and is classified as an excipient/solvent used in parenteral nutrition. The product is authorized for prescription use within the European Union market.

Manufacturer / TM Owner

Deltamedica Gmbh

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Indications & Clinical Uses

Glucose-Lösung Deltamedica is employed in clinical settings where rapid carbohydrate delivery is required. It supports several therapeutic objectives:

  • Treatment of hypoglycemia by raising blood glucose levels.
  • Provision of an energy substrate during parenteral nutrition.
  • Fluid and electrolyte replacement in patients unable to take oral intake.
  • Support during perioperative care to maintain glucose homeostasis.
  • Adjunctive therapy in critical care for metabolic support.

Side Effects

Glucose-Lösung Deltamedica may be associated with a range of adverse reactions, most of which are related to its intravenous administration.

Common

  • Local irritation at the infusion site.
  • Mild hyperglycemia.
  • Nausea or vomiting.
  • Transient electrolyte imbalance.

Serious

  • Severe hyperglycemia leading to osmotic diuresis.
  • Allergic or anaphylactic reaction.
  • Phlebitis or thrombophlebitis.
  • Fluid overload, especially in patients with cardiac or renal impairment.

Precautions & Warnings

When using Glucose-Lösung Deltamedica, clinicians should consider several safety measures to minimize risk:

  • Assess blood glucose levels before and during infusion.
  • Adjust infusion rate in patients with diabetes or impaired glucose tolerance.
  • Monitor fluid balance to avoid overload in heart failure or renal disease.
  • Use aseptic technique to prevent contamination and infection.
  • Evaluate electrolyte status, particularly sodium and potassium, during therapy.
  • Document any signs of hypersensitivity promptly.

Avoid Interactions

Glucose-Lösung Deltamedica can interact with other medications or clinical conditions, requiring careful management.

Avoid

  • Concurrent administration of high‑dose insulin without appropriate glucose monitoring.
  • Co‑infusion with solutions containing incompatible electrolytes (e.g., calcium chloride).

Use with caution

  • Beta‑blockers, which may mask hypoglycemia symptoms.
  • Corticosteroids, which can increase blood glucose levels.
  • Diuretics that may alter fluid and electrolyte balance.
  • Medications that affect renal function, such as ACE inhibitors.

Frequently Asked Questions

The primary indication is the treatment of hypoglycemia by providing an immediate source of glucose through intravenous infusion.

It is administered intravenously as a sterile solution for injection, typically via a peripheral or central venous line, with the rate adjusted to the patient’s glucose and fluid needs.

Yes, but dosing and infusion rates must be carefully monitored and coordinated with insulin therapy to avoid excessive hyperglycemia.

Blood glucose levels, electrolyte concentrations, and overall fluid balance should be monitored regularly throughout the infusion.

Compatibility depends on the specific solution; it should not be mixed with calcium-containing solutions or other incompatible electrolytes without verification.

Signs may include rash, itching, swelling, difficulty breathing, or anaphylaxis, and require immediate medical attention.

It supplies a carbohydrate substrate that can be metabolized for energy, forming a key component of total parenteral nutrition regimens.

Use in children is possible but must follow pediatric dosing guidelines and close monitoring of glucose and fluid status.

Fluid overload risk is higher; infusion rates should be limited and fluid balance closely tracked.

The product is a sterile aqueous solution of glucose anhydrous and does not contain additional preservatives.

It is classified under ATC code B05AA02, which denotes glucose solutions used for parenteral nutrition.

Yes, it is a prescription‑only medication in the European Union.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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