Product image of Glucosum Teva (Glucose) supplied by GNH India

Glucosum Teva

Active Ingredient:
Glucose
Origin:
EU

Glucosum Teva (Glucose)

Glucosum Teva is a sterile intravenous injection solution that contains glucose as its active ingredient. It is supplied in a standard concentration (strength not specified) and is classified as a carbohydrate solution used as an excipient. Marketed in the European Union and available by prescription, Glucosum Teva provides a rapid source of glucose for patients who require intravenous energy support or fluid replacement in clinical settings.

Manufacturer / TM Owner

Teva Pharmaceuticals Polska Sp. Z O.O.

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Indications & Clinical Uses

Glucosum Teva is indicated for several clinical situations where rapid elevation of plasma glucose or fluid replacement is required.

  • Treatment of acute hypoglycemia when oral glucose is not feasible.
  • Component of parenteral nutrition regimens for patients unable to eat or absorb nutrients.
  • Fluid and electrolyte replacement in peri‑operative or critical‑care settings.
  • Dilution medium for certain intravenous medications that require a carbohydrate carrier.
  • Supportive therapy during prolonged fasting or severe malnutrition.

Side Effects

Adverse reactions to Glucosum Teva are generally related to the intravenous administration of a glucose solution.

Common

  • Mild hyperglycemia or transient rise in blood glucose levels.
  • Local irritation or pain at the injection site.
  • Nausea or mild gastrointestinal discomfort.

Serious

  • Severe hyperglycemia with possible osmotic diuresis.
  • Electrolyte imbalance, particularly hyponatremia or hyperkalemia.
  • Allergic reaction ranging from urticaria to anaphylaxis.

Precautions & Warnings

When using Glucosum Teva, clinicians should consider several safety factors to minimize risk.

  • Assess baseline blood glucose and monitor levels during and after infusion.
  • Adjust dosage in patients with diabetes mellitus or impaired glucose tolerance.
  • Use caution in individuals with renal or hepatic dysfunction, as metabolism may be altered.
  • Avoid rapid infusion in neonates and infants to prevent circulatory overload.
  • Ensure proper aseptic technique to reduce the risk of infection.
  • Review electrolyte status before administration, especially in patients receiving large volumes.

Avoid Interactions

Glucosum Teva may interact with other agents that affect glucose metabolism or fluid balance.

Avoid

  • Concurrent use of high‑dose insulin without appropriate glucose monitoring.
  • Co‑administration with other hypertonic glucose solutions, which can exacerbate hyperglycemia.

Use with caution

  • Diuretic therapy that may influence electrolyte levels.
  • Beta‑blockers, which can mask symptoms of hypoglycemia.
  • Corticosteroids, as they may increase glucose production.
  • Medications that cause fluid retention, such as certain antihypertensives.

Frequently Asked Questions

Glucosum Teva contains glucose as its sole active ingredient, providing an immediate source of carbohydrate when administered intravenously.

It is commonly prescribed for acute hypoglycemia, as part of parenteral nutrition, and for fluid and electrolyte replacement in peri‑operative or critical‑care settings.

Glucosum Teva is given as an intravenous injection or infusion, following aseptic technique and appropriate infusion rate guidelines.

Yes, but blood glucose should be closely monitored and the infusion rate adjusted to avoid excessive hyperglycemia.

Regular monitoring of blood glucose, electrolytes, and fluid balance is recommended throughout the infusion period.

Glucosum Teva should be avoided in patients with known hypersensitivity to glucose solutions and in those where rapid fluid overload could be harmful.

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

Serious reactions may include severe hyperglycemia, electrolyte disturbances, and allergic reactions such as anaphylaxis.

Store the product at controlled room temperature, protected from light, and keep it in the original packaging until administration.

Compatibility should be verified for each medication; some drugs may require separate infusion lines to avoid precipitation or interaction.

Neonates, infants, patients with renal or hepatic impairment, and those with severe electrolyte imbalances may need adjusted infusion rates.

Yes, it can be incorporated into long‑term parenteral nutrition formulas, but regular monitoring of metabolic parameters is essential.

Published by

GNH India Pharmaceuticals Limited

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Last updated:

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