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

Glucotrace

Active Ingredient:
Fludeoxyglucose (18f)
Origin:
EU

Glucotrace (Fludeoxyglucose (18f))

Glucotrace is a radiopharmaceutical solution for injection that contains the active ingredient fludeoxyglucose (18F). It is supplied without a specified strength and is administered intravenously under prescription. As a diagnostic PET imaging agent, Glucotrace acts as a glucose analog that highlights metabolic activity in tissues, enabling clinicians to assess oncologic, cardiac, and neurologic conditions through positron emission tomography.

Manufacturer / TM Owner

Nucleis Sa

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Indications & Clinical Uses

Glucotrace is employed in several PET imaging applications to evaluate metabolic activity in the body. It assists physicians in diagnosing and managing a range of conditions.

  • Oncologic PET imaging for tumor detection, staging, and treatment response assessment.
  • Cardiac PET imaging to evaluate myocardial viability and perfusion.
  • Neurologic PET imaging for brain metabolism studies, including dementia and epilepsy evaluation.
  • Research studies investigating glucose metabolism in various disease models.
  • Companion diagnostic use when paired with targeted therapies.

Side Effects

Adverse reactions to Glucotrace are generally infrequent but may occur following intravenous administration. Most events are mild and transient.

Common

  • Mild injection site discomfort or erythema.
  • Transient nausea or vomiting.
  • Temporary headache.
  • Low-grade fever.
  • Mild allergic skin reactions such as urticaria.

Serious

  • Anaphylactic or severe hypersensitivity reactions.
  • Significant hypotension or cardiovascular collapse.
  • Acute renal impairment in susceptible patients.
  • Severe radiation‑related tissue injury (rare with standard dosing).

Precautions & Warnings

Glucotrace should be used with careful consideration of patient‑specific factors and procedural protocols. Key safety points include:

  • Verify patient identity and confirm indication before administration.
  • Assess renal function, especially in patients with known impairment.
  • Use appropriate radiation protection measures for staff and surrounding individuals.
  • Pregnant or breastfeeding patients should be evaluated for risk versus benefit, as fetal exposure is unknown.
  • Ensure proper handling and disposal of radioactive waste according to local regulations.
  • Monitor patients for immediate adverse reactions during and after injection.

Avoid Interactions

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

Avoid

  • Concurrent administration of high‑dose glucose or dextrose solutions that could compete for cellular uptake.
  • Use of other radiopharmaceuticals within 24 hours that may increase cumulative radiation dose.

Use with caution

  • Medications that alter blood glucose levels (e.g., insulin, oral hypoglycemics) as they may affect tracer distribution.
  • Contrast agents used in CT imaging performed immediately before or after PET, which could affect image interpretation.
  • Drugs that influence renal clearance, potentially modifying tracer elimination.

Frequently Asked Questions

Glucotrace is a fluorine‑18 labeled glucose analog that is taken up by glucose transporters and phosphorylated by hexokinase. Because it cannot undergo further metabolism, it becomes trapped in cells, allowing PET scanners to visualize areas of increased metabolic activity.

Oncologists, cardiologists, and neurologists frequently use Glucotrace for tumor staging, assessment of myocardial viability, and evaluation of brain metabolism, respectively.

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

Yes, but blood glucose levels should be measured and, if necessary, controlled before injection because elevated glucose can compete with the tracer and affect image quality.

Patients are typically instructed to fast for several hours, avoid strenuous activity, and maintain stable blood glucose levels. Specific institutional protocols may vary.

Radiation safety guidelines require the use of shielding, monitoring devices, and proper waste disposal to minimize exposure to personnel handling Glucotrace.

Mild injection site discomfort, transient nausea, headache, low‑grade fever, and occasional mild skin reactions are the most frequently reported side effects.

If an allergic reaction occurs, the injection should be stopped immediately, and standard emergency measures—including administration of antihistamines, corticosteroids, and epinephrine if indicated—should be initiated.

Glucotrace may be used in children when clinically indicated, but dosing and radiation exposure must be carefully calculated according to pediatric guidelines.

A PET scanner equipped to detect positrons emitted by fluorine‑18 is required. The scanner is often combined with CT or MRI for anatomical correlation.

Coverage varies by region and insurer; many health plans reimburse PET imaging when it is medically necessary and ordered by a qualified physician.

Fluorine‑18 has a physical half‑life of approximately 110 minutes, so detectable activity declines rapidly, typically allowing imaging within 60–90 minutes post‑injection.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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