Europe — EMA
Glucose Teva
Glucose Teva is an anhydrous glucose excipient for epidural, intrabursal, and intracoronary use; see indications, safety, and FAQs.
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What is 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.
What is Glucose, Anhydrous used for?
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.
What are the side effects of Glucose, Anhydrous?
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.
What precautions apply to Glucose, Anhydrous?
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.
What does Glucose, Anhydrous interact with?
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
What is the primary function of Glucose Teva in parenteral formulations?+
Can Glucose Teva be used for patients with diabetes?+
Is Glucose Teva approved for intravenous infusion?+
What are the common side effects after administration of Glucose Teva?+
What serious adverse reactions should be reported?+
How should Glucose Teva be stored before use?+
Are there any contraindications for using Glucose Teva?+
What monitoring is recommended during administration?+
Can Glucose Teva be mixed with other injectable drugs?+
What should be done if an allergic reaction occurs?+
Is Glucose Teva considered a medication or an excipient?+
Where is Glucose Teva manufactured and marketed?+
Product details
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