Europe — EMA
Glukóz Teva
Glukóz Teva is an EU‑approved intravenous glucose monohydrate solution used to raise plasma glucose and support metabolic needs in clinical settings.
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What is Glucose Monohydrate?
Glukóz Teva is an intravenous solution that contains glucose monohydrate as its active ingredient. It is supplied in a sterile liquid form for infusion into the bloodstream. The product is manufactured for the European Union market and is used to provide a rapid source of glucose for metabolic needs. Glukóz Teva is typically packaged in single‑use containers suitable for hospital and clinical settings.
What is Glucose Monohydrate used for?
Glukóz Teva is administered intravenously to address acute or temporary needs for glucose. It is commonly employed in the following clinical situations:
- Treatment of hypoglycaemia when oral glucose is not feasible. - Provision of caloric support during peri‑operative fasting. - Management of metabolic demands in critically ill patients. - Support during prolonged intravenous nutrition regimens. - Stabilisation of blood glucose levels in patients receiving insulin therapy. - Adjunct therapy in certain diagnostic procedures requiring glucose infusion.
What are the side effects of Glucose Monohydrate?
Glukóz Teva may cause a range of reactions, most of which are related to the rapid increase in plasma glucose. These effects are generally classified as follows:
Common: - Transient hyperglycaemia. - Local irritation at the infusion site. - Mild nausea or abdominal discomfort. - Headache associated with rapid glucose shifts.
Serious: - Severe hyperglycaemia leading to osmotic diuresis. - Electrolyte imbalances, particularly hyponatraemia. - Allergic reactions such as rash or urticaria. - Volume overload in patients with compromised cardiac function.
What precautions apply to Glucose Monohydrate?
When using Glukóz Teva, healthcare professionals should consider several safety measures to minimise risk:
- Verify patient’s blood glucose level before administration. - Adjust infusion rate in patients with diabetes or impaired glucose tolerance. - Monitor electrolytes, especially sodium and potassium, during prolonged use. - Use caution in patients with renal or cardiac insufficiency due to fluid volume concerns. - Ensure aseptic technique to prevent contamination of the intravenous line. - Review medication history for agents that may potentiate hyperglycaemia.
What does Glucose Monohydrate interact with?
Glukóz Teva can interact with other medications, requiring careful assessment:
Avoid: - Concurrent high‑dose insulin therapy without glucose monitoring. - Co‑administration with sulfonylureas in patients prone to hypoglycaemia.
Use with caution: - Beta‑blockers, which may mask hypoglycaemia symptoms. - Corticosteroids, which can increase glucose production. - Diuretics that affect electrolyte balance. - Medications that cause fluid retention, such as certain antihypertensives.
Frequently asked questions
What is the primary purpose of Glukóz Teva when administered intravenously?+
In which clinical situations is Glukóz Teva commonly used?+
How should blood glucose be monitored when using Glukóz Teva?+
Can Glukóz Teva be given to patients with diabetes?+
What are common side effects associated with intravenous glucose solutions like Glukóz Teva?+
What serious adverse reactions should clinicians watch for?+
Are there any contraindications for using Glukóz Teva?+
How does Glukóz Teva interact with insulin therapy?+
What precautions are needed for patients receiving diuretics?+
Is Glukóz Teva suitable for pediatric patients?+
What storage conditions are recommended for Glukóz Teva?+
Can Glukóz Teva be mixed with other intravenous medications?+
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