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

Glucose Teva

Active Ingredient:
Glucose
Origin:
EU

Glucose Teva (Glucose)

Glucose Teva is a pharmaceutical preparation containing glucose as the sole active ingredient. It is supplied as a sterile solution for epidural, intrabursal, and intracoronary administration. The product is manufactured for the European market and meets EU pharmaceutical standards. It provides a carbohydrate source for clinical situations that specifically require direct tissue exposure.

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

Glucose Teva is employed in clinical settings where a direct source of glucose is needed for local tissue metabolism or procedural support.

  • Provides an immediate carbohydrate substrate during epidural procedures.
  • Serves as an energy source in intrabursal injections for joint interventions.
  • Used as a glucose infusion in intracoronary applications during cardiac catheterisation.
  • Supports metabolic needs of tissues exposed to ischemia in surgical contexts.
  • May be utilised in research protocols requiring sterile glucose solutions.

Side Effects

Adverse reactions to Glucose Teva are generally related to the route of administration and the sterile solution itself.

Common

  • Local pain or discomfort at the injection site.
  • Mild erythema or bruising.
  • Transient headache.
  • Nausea or mild dizziness.
  • Temporary increase in blood glucose levels.

Serious

  • Infection at the administration site.
  • Allergic or hypersensitivity reaction (rash, urticaria, anaphylaxis).
  • Embolism or vascular occlusion.
  • Severe hypotension or cardiovascular instability.
  • Tissue necrosis or ulceration.

Precautions & Warnings

When using Glucose Teva, clinicians should observe standard aseptic technique and consider patient‑specific factors to minimise risk.

  • Verify sterility and integrity of the container before use.
  • Assess patient’s glucose tolerance and diabetic status.
  • Use only the intended routes (epidural, intrabursal, intracoronary); other routes are not approved.
  • Monitor vital signs and blood glucose during and after administration.
  • Avoid administration in patients with known hypersensitivity to glucose solutions.
  • Store according to manufacturer’s instructions to maintain solution stability.

Avoid Interactions

Glucose solutions can interact with other agents administered intravenously or locally; awareness of potential interactions helps ensure safe use.

Avoid

  • Co‑administration with hyperosmolar agents that may increase risk of local tissue injury.
  • Simultaneous injection of particulate suspensions that could precipitate emboli.

Use with caution

  • Concurrent use of insulin or other glucose‑lowering medications; monitor blood glucose closely.
  • Combination with vasoconstrictors that may affect local circulation.
  • Administration alongside contrast media in coronary procedures; observe for additive osmolar load.
  • Use with other epidural drugs that may alter analgesic efficacy or cause additive side effects.

Frequently Asked Questions

Glucose Teva is a sterile glucose solution intended to provide a direct source of carbohydrate during epidural, intrabursal, or intracoronary procedures.

The product is approved for epidural, intrabursal, and intracoronary administration only.

Use in diabetic patients should be considered carefully, with monitoring of blood glucose levels, because the solution adds carbohydrate load.

Store the unopened container at the temperature recommended by the manufacturer, typically between 2 °C and 8 °C, and protect from light.

Glucose Teva is generally classified as a prescription‑only product in the European Union.

Common local reactions include mild pain, erythema, bruising, or transient headache at the injection site.

Signs of infection, severe allergic reaction, embolism, profound hypotension, or tissue necrosis should prompt urgent evaluation.

Mixing is not routinely recommended; compatibility should be confirmed by the manufacturer or a pharmacist before co‑administration.

Yes, it may be used as an intracoronary glucose infusion to support myocardial metabolism during certain catheterisation procedures.

Monitor vital signs, blood glucose, and the injection site for any signs of adverse reactions throughout the procedure and during the recovery period.

Used containers should be disposed of according to local regulations for hazardous medical waste.

Do not use the product; discard it and obtain a new, intact vial to avoid potential contamination.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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