Product image of Glucose Teva (Glucose, Anhydrous) supplied by GNH India

Glucose Teva

Active Ingredient:
Glucose, Anhydrous
Origin:
EU

Glucose Teva (Glucose, Anhydrous)

Glucose Teva is a pharmaceutical‑grade anhydrous glucose produced by Teva and marketed in the European Union. The product contains glucose, anhydrous as the sole active ingredient; specific strength and dosage form are not disclosed. Classified as an excipient, it is intended for parenteral preparations administered via epidural, intrabursal, or intracoronary routes. It is supplied in a sterile container for aseptic use and may serve as an energy or osmotic agent.

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

Glucose Teva is used primarily as an excipient in parenteral formulations where a sterile source of carbohydrate is required.

  • Provides an immediate source of glucose for cellular metabolism during procedures.
  • Serves as an osmotic agent to maintain fluid balance in epidural or intracoronary infusions.
  • Acts as a diluent or carrier for other injectable medications.
  • Facilitates the preparation of isotonic solutions for intrabursal injections.
  • Supports energy requirements in cardiac catheterization procedures.

Side Effects

Adverse reactions to Glucose Teva are generally related to the systemic effects of glucose when administered intravenously or via other parenteral routes.

Common

  • Transient hyperglycemia.
  • Nausea or vomiting.
  • Local irritation at the injection site.
  • Headache.
  • Flushing or warmth sensation.
  • Mild dizziness.

Serious

  • Severe hyperglycemia requiring medical intervention.
  • Anaphylactic or severe allergic reaction.
  • Electrolyte disturbances (e.g., hyponatremia).
  • Pulmonary edema in susceptible patients.
  • Seizures secondary to extreme glucose shifts.
  • Hypoglycemia if glucose is over‑corrected in diabetic patients.

Precautions & Warnings

When using Glucose Teva, clinicians should consider patient‑specific factors and monitor for potential complications.

  • Assess baseline blood glucose and adjust dosing in diabetic or hypoglycemic patients.
  • Use caution in patients with renal or hepatic impairment due to altered glucose metabolism.
  • Monitor electrolytes, especially sodium and potassium, during large volume administrations.
  • Avoid rapid infusion rates that may cause fluid overload or osmotic shifts.
  • Ensure sterile technique to prevent contamination of the product.
  • Review patient allergy history before administration.

Avoid Interactions

Glucose Teva may interact with other agents that affect blood glucose levels or fluid balance.

Avoid

  • Concurrent high‑dose insulin therapy without glucose monitoring.
  • Co‑administration with other hyperosmolar solutions that could exacerbate fluid shifts.
  • Use with medications that cause severe hypoglycemia (e.g., sulfonylureas) without close monitoring.

Use with caution

  • Beta‑blockers, which may mask hypoglycemia symptoms.
  • Diuretics that alter electrolyte status.
  • Corticosteroids, which can increase glucose production.
  • Cardiac glycosides, where fluid overload may affect cardiac function.

Frequently Asked Questions

Glucose Teva provides a sterile source of glucose that can serve as an energy substrate, osmotic agent, or diluent in injectable preparations.

Yes, but blood‑glucose levels should be closely monitored and dosing adjusted, as the product can raise plasma glucose concentrations.

Glucose Teva is marketed for epidural, intrabursal, and intracoronary routes; intravenous use follows the same safety principles but should be guided by clinical judgment.

Common side effects include transient hyperglycemia, nausea, local irritation, headache, flushing, and mild dizziness.

Serious reactions such as severe hyperglycemia, anaphylaxis, electrolyte imbalance, pulmonary edema, seizures, or hypoglycemia require immediate medical attention.

Store the product in a controlled‑temperature environment, protected from light, and keep the container sealed until ready for aseptic preparation.

There are no absolute contraindications, but caution is advised in patients with uncontrolled diabetes, severe renal or hepatic disease, and known hypersensitivity to glucose solutions.

Monitor blood glucose, electrolytes, and fluid balance; observe the injection site for irritation and watch for signs of allergic reaction.

It can be used as a carrier for many injectable agents, but compatibility should be verified, especially with drugs that affect osmolarity or glucose metabolism.

Discontinue the infusion, provide appropriate emergency treatment such as antihistamines or epinephrine, and report the event to the healthcare provider.

Glucose Teva is classified as an excipient; it does not have a therapeutic claim on its own but supports the delivery of other drugs.

The product is manufactured by Teva and marketed within the European Union.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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