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

Glucotrace

Active Ingredient:
Fludeoxyglucose (18f)
Origin:
EU

Glucotrace (Fludeoxyglucose (18f))

Glucotrace is a radiopharmaceutical containing the active ingredient fludeoxyglucose (18F) supplied as a sterile solution for injection. It is administered intravenously under prescription and is used primarily in positron emission tomography (PET) imaging to visualize metabolic activity in various tissues. The product is marketed in the European Union and belongs to the diagnostic imaging agent class.

Manufacturer / TM Owner

Nucleis Sa

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Indications & Clinical Uses

Glucotrace is indicated for several PET imaging applications that require assessment of cellular glucose metabolism. It helps clinicians evaluate disease presence and progression in specific organ systems.

  • Oncologic PET imaging for detection, staging, and monitoring of malignant tumors.
  • Cardiac PET imaging to assess myocardial viability and perfusion.
  • Neurologic PET imaging for epilepsy, dementia, and movement disorders.
  • Research studies investigating metabolic pathways in vivo.
  • Whole‑body PET scans for comprehensive disease assessment.

Side Effects

Adverse reactions to Glucotrace are generally mild and related to the radiopharmaceutical nature of the product. Serious events are rare but may occur.

Common

  • Transient flushing or warmth sensation at the injection site.
  • Mild nausea or vomiting.
  • Temporary headache.
  • Short‑lasting dizziness.
  • Mild allergic skin reactions (e.g., erythema).

Serious

  • Severe hypersensitivity or anaphylaxis.
  • Significant radiation‑induced tissue injury (extremely rare).
  • Prolonged hypotension.
  • Acute renal impairment in patients with pre‑existing kidney disease.

Precautions & Warnings

Glucotrace should be used with careful consideration of patient‑specific factors and procedural requirements. The following precautions are recommended:

  • Verify pregnancy status; avoid use in pregnant women unless the diagnostic benefit outweighs potential fetal radiation exposure.
  • Assess renal function before administration, especially in patients with known kidney disease.
  • Ensure proper hydration to facilitate radiotracer clearance.
  • Observe radiation safety protocols for staff and surrounding individuals.
  • Review patient history for prior allergic reactions to radiopharmaceuticals.
  • Adjust dosage for pediatric patients according to weight‑based guidelines.
  • Document and monitor any adverse events promptly.

Avoid Interactions

Glucotrace may interact with other agents that affect glucose metabolism or radiation exposure. Consider the following:

Avoid

  • High‑dose glucose or insulin therapy immediately before the scan, which can alter tracer uptake.
  • Concurrent administration of other radiopharmaceuticals that may confound PET image interpretation.

Use with caution

  • Medications that modify blood glucose levels (e.g., metformin, sulfonylureas) – consider temporary discontinuation per protocol.
  • Contrast agents used in CT components of PET/CT studies – assess cumulative radiation dose.
  • Chemotherapeutic agents that affect tumor metabolism – timing of imaging may need adjustment.
  • Beta‑blockers or other cardiovascular drugs that could influence myocardial uptake.
  • Any investigational drugs in clinical trials – coordinate with study investigators.

Frequently Asked Questions

Glucotrace is a glucose analog that enters metabolically active cells via glucose transporters, is phosphorylated by hexokinase, and becomes trapped because it cannot undergo further metabolism, emitting positrons detectable by PET scanners.

Oncology, cardiology, and neurology are the primary specialties that use Glucotrace to assess tumor metabolism, myocardial viability, and brain disorders such as epilepsy or dementia.

Glucotrace is supplied as a sterile solution for injection and is administered intravenously under the supervision of qualified nuclear medicine personnel.

Use in pregnancy is generally avoided because the radiotracer delivers ionizing radiation; it may be considered only when the diagnostic benefit clearly outweighs potential fetal risk.

Patients are typically instructed to fast for several hours, maintain normal hydration, and avoid high‑dose glucose or insulin therapy prior to the scan to ensure optimal tracer uptake.

Common side effects include transient flushing, mild nausea, brief headache, dizziness, and mild skin redness at the injection site.

Contraindications include known hypersensitivity to fludeoxyglucose or any component of the formulation, and situations where radiation exposure is unacceptable, such as in certain pregnant patients.

The positron emission from fludeoxyglucose (18F) has a physical half‑life of approximately 110 minutes, allowing imaging typically within 60–90 minutes post‑injection.

Staff must follow radiation protection guidelines, including wearing lead aprons, using shielding, monitoring exposure with dosimeters, and adhering to proper waste disposal procedures.

It can be combined with CT contrast in PET/CT studies, but cumulative radiation dose should be evaluated and protocols adjusted accordingly.

Glucotrace may be used in children when weight‑based dosing is applied and the clinical indication justifies the radiation exposure, following local regulatory guidance.

A physician’s order, patient consent, verification of pregnancy status, renal function assessment, and a completed radiation safety checklist are typically required.

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GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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