Product image of Gluscan (Fludeoxyglucose (18f)) supplied by GNH India

Gluscan

Active Ingredient:
Fludeoxyglucose (18f)
Origin:
EU

Gluscan (Fludeoxyglucose (18f))

Gluscan is a radiopharmaceutical product that contains the active ingredient fluorodeoxyglucose labeled with fluorine‑18 (18F‑FDG) in a sterile solution for injection. It is supplied in an injectable form without a specified strength on the label and is authorized for prescription use within the European Union. Gluscan functions as a glucose analog that enables visualization of metabolic and quantitative activity during clinical PET imaging diagnostic procedures.

Manufacturer / TM Owner

Advanced Accelerator Applications Molecular Imaging France S.A.S.

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Indications & Clinical Uses

Gluscan is employed as a diagnostic imaging agent in positron emission tomography (PET) to assess metabolic activity in various clinical contexts.

  • Oncologic PET imaging for tumor detection, staging, and therapeutic monitoring.
  • Cardiac PET imaging to evaluate myocardial viability and perfusion.
  • Neurologic PET imaging for assessment of epilepsy foci, dementia, and other brain disorders.
  • Research applications involving quantitative measurement of glucose metabolism in clinical trials.
  • Evaluation of inflammatory diseases where increased metabolic activity may indicate active inflammation.

Side Effects

Adverse reactions to Gluscan are generally infrequent, but they can be categorized by frequency and severity.

Common

  • Transient flushing or warmth sensation at the injection site.
  • Mild nausea or vomiting shortly after administration.
  • Short‑lasting headache or dizziness.
  • Temporary metallic taste in the mouth.
  • Mild fatigue or feeling of weakness.
  • Minor injection site discomfort.

Serious

  • Allergic reactions ranging from urticaria to anaphylaxis.
  • Severe hypoglycemia in patients with impaired glucose regulation.
  • Radiation‑related tissue injury in rare high‑dose exposures.
  • Cardiac arrhythmia triggered by metabolic stress.
  • Persistent neurological symptoms such as seizures in susceptible individuals.

Precautions & Warnings

Prior to administering Gluscan, clinicians should evaluate patient-specific factors and follow safety guidelines to minimize risks.

  • Verify blood glucose level is within an acceptable range before injection.
  • Assess for known hypersensitivity to fluorodeoxyglucose or any component of the formulation.
  • Consider pregnancy and lactation status; use only if the diagnostic benefit outweighs potential fetal exposure.
  • Ensure appropriate radiation protection measures for staff and nearby individuals.
  • Adjust dosing for pediatric patients according to weight‑based protocols when applicable.
  • Review recent administration of other radiopharmaceuticals to avoid cumulative radiation dose.

Avoid Interactions

Gluscan may interact with certain medications or conditions that affect glucose metabolism or radiation exposure.

Avoid

  • Concurrent use of high‑dose insulin or oral hypoglycemic agents that could cause severe hypoglycemia.
  • Administration of other radiopharmaceuticals within a short interval, which may increase cumulative radiation dose.

Use with caution

  • Patients receiving chemotherapy or targeted therapies that alter tumor metabolism.
  • Use in individuals with renal impairment affecting clearance of the tracer.
  • Concurrent contrast agents for CT may affect image interpretation; schedule appropriately.
  • Beta‑blockers or other drugs influencing myocardial glucose uptake in cardiac studies.
  • Medications that significantly alter systemic glucose levels, such as corticosteroids.

Frequently Asked Questions

Gluscan is a radiopharmaceutical that contains fluorodeoxyglucose labeled with fluorine‑18. It acts as a glucose analog that is taken up by metabolically active cells, phosphorylated, and trapped, producing a PET signal that reflects tissue metabolism.

Gluscan is routinely used in oncology for tumor detection and staging, in cardiology to assess myocardial viability, and in neurology for evaluating epilepsy, dementia, and other brain disorders.

Yes, Gluscan is authorized as a prescription‑only radiopharmaceutical for PET imaging within the EU market.

Gluscan is supplied as a sterile solution for injection and is administered intravenously under controlled conditions by qualified healthcare professionals.

Patients should have their blood glucose level checked, fast as instructed, and inform the provider of any allergies, pregnancy, or recent radiopharmaceutical exposure.

Gluscan may be used in pediatric patients when a weight‑based dosing protocol is applied and the diagnostic benefit justifies the radiation exposure.

Common side effects include transient flushing, mild nausea, short‑lasting headache, a metallic taste, mild fatigue, and minor injection site discomfort.

Serious reactions such as allergic responses (including anaphylaxis), severe hypoglycemia, radiation‑related tissue injury, or cardiac arrhythmias must be reported immediately to medical personnel.

Gluscan should only be used during pregnancy or lactation when the diagnostic benefit outweighs potential risks to the fetus or infant, and appropriate precautions are taken.

Concurrent high‑dose insulin or certain oral hypoglycemics can increase the risk of severe hypoglycemia; dosing and timing should be coordinated with the treating physician.

Yes, standard radiation safety protocols are followed, including limiting close contact with vulnerable individuals for a short period after the scan, as recommended by local regulations.

When CT contrast agents are required, they should be scheduled appropriately because they can affect PET image interpretation; coordination between imaging teams is essential.

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GNH India Pharmaceuticals Limited

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Last updated:

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