GNH USA

Europe — EMA

Gluscan

Gluscan is a prescription radiopharmaceutical (fludeoxyglucose 18F) used for PET imaging in oncology, cardiology, and neurology.

Fludeoxyglucose (18f)

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What is Fludeoxyglucose (18f)?

Gluscan is a radiopharmaceutical product containing the active ingredient fludeoxyglucose (18F) supplied as a sterile solution for injection. It is marketed in the European Union and is available only by prescription. The compound is a fluorine‑18 labeled glucose analog used in positron emission tomography (PET) imaging to assess metabolic activity in various tissues. Gluscan is administered intravenously under controlled conditions and interpreted by qualified physicians.

What is Fludeoxyglucose (18f) used for?

Gluscan is indicated for diagnostic PET imaging in several clinical specialties.

- Oncologic PET imaging for tumor detection, staging, and treatment monitoring - Cardiac PET imaging to assess myocardial viability and perfusion - Neurologic PET imaging for brain metabolism, epilepsy evaluation, and dementia assessment - Pediatric oncology imaging when appropriate and dose‑adjusted - Research applications such as pharmacokinetic and drug‑development studies

What are the side effects of Fludeoxyglucose (18f)?

Adverse reactions to Gluscan are generally mild, but rare serious events have been reported.

Common: - Nausea or mild gastrointestinal discomfort - Transient flushing or warmth at the injection site - Injection site pain or bruising - Mild headache or dizziness

Serious: - Allergic reactions including anaphylaxis - Severe hypoglycemia, especially in diabetic patients - Radiation‑related skin erythema or ulceration - Acute renal impairment in susceptible individuals

What precautions apply to Fludeoxyglucose (18f)?

Use of Gluscan requires careful consideration of patient‑specific factors and procedural safeguards.

- Verify pregnancy status and defer use unless benefits outweigh risks - Ensure adequate patient hydration before and after injection - Check fasting blood glucose levels; correct significant hyper‑ or hypoglycemia - Apply standard radiation protection measures for staff and family members - Avoid use in patients with known severe allergy to radiopharmaceuticals - Adjust dosing for pediatric patients according to weight or surface area - Review recent exposure to other radiopharmaceuticals or high‑dose imaging studies

What does Fludeoxyglucose (18f) interact with?

Gluscan may interact with other agents that affect glucose metabolism or radiation exposure.

Avoid: - Concurrent administration of high‑dose iodinated contrast agents within 24 hours - Use of another PET radiotracer within 24 hours of Gluscan injection

Use with caution: - Antidiabetic medications (insulin, sulfonylureas, metformin) that may alter glucose levels - Drugs that modify myocardial perfusion (e.g., vasodilators, beta‑blockers) - Recent chemotherapy or radiotherapy that could affect tissue uptake - Agents that increase serum calcium or phosphate levels - Substances influencing renal clearance such as diuretics or nephrotoxic drugs

Frequently asked questions

What is the mechanism of action of Gluscan in PET imaging?+
Gluscan contains fludeoxyglucose (18F), a glucose analog that is taken up by metabolically active cells and phosphorylated but not further metabolized, leading to accumulation in tissues that emit positrons detectable by PET scanners.
How is Gluscan administered for oncologic PET scans?+
Gluscan is injected intravenously as a sterile solution. The dose is calculated based on patient weight or body surface area, followed by a waiting period (typically 60 minutes) before PET image acquisition.
Which clinical conditions can be evaluated with Gluscan cardiac PET imaging?+
Gluscan cardiac PET imaging assesses myocardial viability, perfusion defects, and can help differentiate viable myocardium from scar tissue in patients with coronary artery disease or heart failure.
Can Gluscan be used in pediatric patients?+
Gluscan may be used in children when clinically indicated, but dosing is adjusted for weight or surface area, and the benefit‑risk ratio must be carefully evaluated by the ordering physician.
What preparation is required before receiving a Gluscan PET scan?+
Patients are usually asked to fast for at least 4–6 hours, maintain normal hydration, and have blood glucose measured prior to injection to ensure optimal image quality.
How does Gluscan differ from other FDG PET tracers?+
Gluscan is a specific brand of fludeoxyglucose (18F) formulated for injection in the EU market; its purity, sterility, and regulatory specifications may differ from other manufacturers but its imaging properties are comparable.
What are the common side effects reported after Gluscan injection?+
Common side effects include mild nausea, transient flushing, injection‑site discomfort, and occasional headache. These effects are usually short‑lived and resolve without intervention.
Are there any contraindications for Gluscan in pregnant women?+
Gluscan is generally contraindicated during pregnancy because the radioactive fluorine‑18 may pose a risk to the fetus; it should only be used if the diagnostic benefit clearly outweighs potential harm.
How should Gluscan be stored and handled in a clinical setting?+
Gluscan must be stored in a lead‑shielded container at controlled temperature (typically 2–8 °C) and protected from light. Personnel should follow radiation safety protocols during preparation and administration.
What radiation safety measures are recommended when using Gluscan?+
Standard precautions include using lead shielding, limiting time of exposure for staff, maintaining distance from the patient after injection, and monitoring radiation dose with appropriate badges.
How long does it take to obtain PET images after Gluscan injection?+
Imaging usually begins 60 ± 10 minutes after injection, allowing sufficient tracer uptake and clearance of background activity for optimal image contrast.
Can Gluscan be combined with other imaging agents in the same study?+
Combining Gluscan with other radiopharmaceuticals in a single session is generally avoided due to potential interference; if needed, adequate time intervals between agents should be observed as per institutional protocols.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Fludeoxyglucose (18f)
Route
Intravenous Use
Manufacturer
Advanced Accelerator Applications Molecular Imaging France S.A.S.
Origin
EU

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