Product image of Glucosteril (Glucose Monohydrate) supplied by GNH India

Glucosteril

Active Ingredient:
Glucose Monohydrate
Origin:
EU

Glucosteril (Glucose Monohydrate)

Glucosteril is a sterile solution for injection that contains glucose monohydrate as its active ingredient. It is supplied in an unspecified strength and is manufactured for the European Union market. The product is classified as an excipient used in parenteral nutrition, providing a source of carbohydrate energy when administered intravenously.

Manufacturer / TM Owner

Fresenius Kabi Deutschland Gmbh

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Indications & Clinical Uses

Glucosteril is employed as a component of intravenous nutrition regimens and as a source of rapid carbohydrate supplementation. It may be used in clinical settings where patients require energy support through the bloodstream.

  • Supplemental carbohydrate source in total parenteral nutrition (TPN)
  • Energy provision during perioperative fasting
  • Management of hypoglycemia when oral intake is not possible
  • Support for patients with increased metabolic demand
  • Adjunct in fluid resuscitation protocols requiring caloric input

Side Effects

Glucosteril is generally well tolerated, but adverse reactions can occur. Reported events are categorized by frequency and severity.

Common

  • Local irritation at the injection site
  • Mild hyperglycemia
  • Transient electrolyte shifts
  • Nausea or vomiting
  • Headache

Serious

  • Severe hyperglycemia leading to osmotic diuresis
  • Allergic reaction or anaphylaxis
  • Metabolic acidosis in susceptible patients
  • Fluid overload with pulmonary edema

Precautions & Warnings

When using Glucosteril, clinicians should consider patient-specific factors and monitor relevant parameters to minimize risks.

  • Assess blood glucose levels before and during infusion
  • Adjust dosage in patients with renal or hepatic impairment
  • Monitor for signs of fluid overload, especially in heart failure
  • Use caution in diabetic patients or those on insulin therapy
  • Verify compatibility with other intravenous solutions
  • Ensure aseptic technique to prevent infection
  • Document any adverse reactions promptly

Avoid Interactions

Glucosteril may interact with other medications or solutions administered intravenously. Awareness of these interactions helps maintain safety.

Avoid

  • Co-administration with high‑dose insulin without glucose monitoring
  • Mixing with incompatible electrolytes that may precipitate
  • Simultaneous infusion of hypertonic dextrose solutions exceeding recommended concentrations

Use with caution

  • Concurrent use of diuretics that affect fluid balance
  • Medications that alter glucose metabolism (e.g., glucocorticoids)
  • Intravenous lipid emulsions that may affect caloric calculations
  • Drugs that require strict electrolyte control (e.g., potassium‑sparing agents)

Frequently Asked Questions

Glucosteril provides a sterile source of glucose monohydrate for intravenous administration, supplying carbohydrate energy as part of parenteral nutrition or when oral intake is not feasible.

Glucosteril is supplied as a solution for injection and is administered intravenously, typically through a peripheral or central venous line under aseptic conditions.

Yes, Glucosteril can be used to raise blood glucose levels in patients with hypoglycemia when oral glucose is not an option, but monitoring is essential.

Blood glucose, electrolyte levels, and fluid balance should be regularly monitored, especially in patients with diabetes, renal impairment, or heart failure.

Compatibility should be confirmed for each specific fluid; some electrolytes or high‑concentration dextrose solutions may be incompatible.

Common side effects include mild hyperglycemia, local irritation at the injection site, transient electrolyte changes, nausea, and headache.

Serious reactions can include severe hyperglycemia, anaphylaxis, metabolic acidosis, and fluid overload leading to pulmonary edema.

Glucosteril should be used with caution in patients on high‑dose insulin, and glucose levels must be closely monitored to prevent hypoglycemia.

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

The regulatory status of Glucosteril varies by region; in many jurisdictions it is supplied by prescription for use in clinical settings.

Use in pediatric patients should follow specific clinical guidelines and dosing recommendations provided by a healthcare professional.

The infusion should be stopped immediately, and appropriate emergency measures, such as administration of antihistamines or epinephrine, should be taken.

Published by

GNH India Pharmaceuticals Limited

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Last updated:

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