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Glucose Sterop

Active Ingredient:
Glucose Monohydrate
Origin:
EU

Glucose Sterop (Glucose Monohydrate)

Glucose Sterop is a sterile intravenous solution containing glucose monohydrate as the active ingredient; the product is supplied in an unspecified strength and is formulated as a solution for injection. It is classified as a carbohydrate solution and is used as a volume expander and an energy source in clinical settings across the European Union. It is available by prescription only and is intended for use under medical supervision.

Manufacturer / TM Owner

Laboratoires Sterop

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Indications & Clinical Uses

Glucose Sterop is indicated for several clinical situations where rapid glucose delivery or plasma volume expansion is required.

  • Treatment of hypoglycemia when oral glucose is not feasible.
  • Fluid and electrolyte replacement in patients needing isotonic solutions.
  • Parenteral nutrition as a carbohydrate source in total or supplemental feeding.
  • Intraoperative glucose supplementation to maintain blood glucose levels during surgery.
  • Support of hemodynamic stability in trauma or burn patients through osmotic volume expansion.

Side Effects

Adverse reactions to Glucose Sterop are generally related to its osmotic and metabolic properties.

Common

  • Mild hyperglycemia, especially with large-volume infusions.
  • Local irritation or pain at the injection site.
  • Nausea or vomiting.
  • Electrolyte disturbances such as hyponatremia.
  • Transient increase in serum osmolality.

Serious

  • Severe hyperglycemia leading to osmotic diuresis.
  • Fluid overload with pulmonary edema.
  • Allergic reactions ranging from urticaria to anaphylaxis.
  • Hyperosmolar hyperglycemic state in susceptible patients.
  • Metabolic acidosis in cases of massive infusion.

Precautions & Warnings

When prescribing Glucose Sterop, clinicians should consider several safety factors to minimize risk.

  • Assess baseline blood glucose and adjust infusion rate accordingly.
  • Monitor serum electrolytes, particularly sodium and potassium, during therapy.
  • Use caution in patients with renal or cardiac insufficiency due to risk of fluid overload.
  • Avoid rapid infusion in neonates and infants because of immature metabolic capacity.
  • Evaluate for a history of hypersensitivity to glucose solutions before administration.
  • Consider alternative carbohydrate sources in patients with uncontrolled diabetes.
  • Ensure proper aseptic technique to prevent contamination.

Avoid Interactions

Glucose Sterop may interact with other agents that affect glucose metabolism or fluid balance.

Avoid

  • Concurrent high-dose insulin therapy without close glucose monitoring.
  • Other hypertonic carbohydrate solutions that could exacerbate hyperglycemia.
  • Sodium-containing fluids in excess, increasing risk of hypernatremia.

Use with caution

  • Diuretics, which may alter electrolyte status during volume expansion.
  • Corticosteroids, which can raise blood glucose levels.
  • Beta‑adrenergic agonists that may affect glucose utilization.
  • Renal replacement therapies that modify fluid and electrolyte balance.

Frequently Asked Questions

Glucose Sterop contains glucose monohydrate as its sole active ingredient.

It is commonly used for treating hypoglycemia, providing fluid and electrolyte replacement, supporting parenteral nutrition, and supplying intraoperative glucose supplementation.

Glucose Sterop is administered intravenously as a sterile solution for injection.

Use in neonates and infants requires caution due to their limited metabolic capacity; dosing and infusion rates should be carefully adjusted.

Blood glucose levels, serum electrolytes, and fluid balance should be regularly monitored to detect hyperglycemia, electrolyte shifts, or fluid overload.

No, Glucose Sterop is a prescription‑only medication and must be prescribed by a qualified healthcare professional.

Common side effects include mild hyperglycemia, local irritation at the injection site, nausea, vomiting, and transient changes in serum osmolality.

Serious reactions may include severe hyperglycemia, fluid overload with pulmonary edema, allergic reactions such as anaphylaxis, hyperosmolar hyperglycemic state, and metabolic acidosis.

Concurrent high‑dose insulin therapy should be avoided without close glucose monitoring, as it can precipitate severe hypoglycemia.

Glucose monohydrate creates an osmotic gradient that draws water into the vascular compartment, thereby expanding plasma volume.

Patients with renal or cardiac insufficiency require careful monitoring because they are at increased risk for fluid overload.

The pregnancy safety category for Glucose Sterop is listed as unknown; it should be used only if clearly needed and prescribed by a physician.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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