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

Metatrace Fdg

Active Ingredient:
Fludeoxyglucose (18f)
Origin:
EU

Metatrace Fdg (Fludeoxyglucose (18f))

Fludeoxyglucose (18F), the active ingredient in Metatrace Fdg, is a radiopharmaceutical presented as a solution for injection for intravenous use. It is used in diagnostic imaging to visualize metabolically active tissues in patients undergoing oncologic, cardiac, or neurologic PET scans.

GNH India supplies Metatrace Fdg as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, oncology centres, and clinics worldwide.

Manufacturer / TM Owner

Siemens Healthcare Gmbh

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Indications & Clinical Uses

Metatrace Fdg, a fluorodeoxyglucose radiotracer, is employed in PET imaging to assess metabolic activity in various clinical settings.

  • Oncologic PET imaging: enables tumor detection, staging, and treatment monitoring by highlighting areas of increased glucose metabolism.
  • Cardiac PET imaging: assesses myocardial viability and perfusion by visualizing glucose uptake in heart muscle.
  • Neurologic PET imaging: aids evaluation of epilepsy and dementia by detecting abnormal cerebral glucose metabolism.

How It Works

  • Fludeoxyglucose (18F) is a structural analogue of glucose that enters cells via GLUT transporters. Once inside, hexokinase phosphorylates it to FDG‑6‑phosphate, which cannot undergo further metabolism and becomes trapped in metabolically active cells. The fluorine‑18 isotope decays by emitting positrons, which are detected by PET scanners to generate images of tissue glucose utilization.

Side Effects

Common Side Effects

  • Injection site pain: mild discomfort at the venipuncture site.
  • Nausea: transient feeling of queasiness.
  • Transient flushing: brief warmth or redness.
  • Mild headache: short‑lasting headache after injection.
  • Warm sensation: temporary feeling of warmth.
  • Mild fatigue: short‑term tiredness.

Serious or Rare Side Effects

  • Allergic reaction: includes rash, itching, or anaphylaxis.
  • Severe hypoglycemia: low blood sugar, especially in diabetic patients.
  • Radiation‑induced tissue injury: rare but possible with high cumulative exposure.
  • Pregnancy exposure risk: potential fetal radiation dose.
  • Nephrogenic toxicity: rare kidney impairment.
  • Severe hypotension: sudden drop in blood pressure.

Precautions & Warnings

Precautions should be observed before and after administration of Metatrace Fdg.

  • Pregnancy: avoid unless clearly needed; fetal risk is unknown.
  • Breastfeeding: discontinue nursing or consider alternative imaging.
  • Diabetes: high blood glucose may affect image quality; consider glucose control.
  • Renal impairment: monitor because excretion may be altered.
  • Radiation safety: follow institutional protocols to limit exposure to staff and patient.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Potential drug interactions must be reviewed prior to use.

Major Interactions (Avoid)

  • High glucose intake: oral glucose or dextrose solutions shortly before the scan can reduce tracer uptake.
  • Insulin therapy: may alter FDG distribution; timing adjustments are required.
  • Iodinated contrast agents: administration within 24 hours may affect image quality.

Moderate Interactions (Monitor Closely)

  • Metformin and other glucose‑lowering agents: may need temporary discontinuation to avoid altered uptake.
  • Beta‑blockers: can influence myocardial FDG uptake.
  • Corticosteroids: may modify inflammatory tissue uptake.

Frequently Asked Questions

Metatrace Fdg is a fluorodeoxyglucose (FDG) radiotracer used in positron emission tomography (PET) scans. It helps visualize metabolic activity in tissues, supporting oncologic tumor detection and staging, cardiac viability assessment, and neurologic evaluation of conditions such as epilepsy and dementia.

Fludeoxyglucose (18F) mimics glucose and is taken up by cells via glucose transporters. Inside the cell, it is phosphorylated and becomes trapped, emitting positrons as the fluorine‑18 decays. PET scanners detect these emissions, producing images that reflect tissue glucose metabolism.

The administered activity of Metatrace Fdg is determined by the prescribing physician based on the patient’s weight, the specific imaging protocol, and the diagnostic indication. Exact dosing is individualized and should follow institutional PET imaging guidelines.

Safety data for Fludeoxyglucose (18F) during pregnancy and lactation are limited. Because the product involves ionizing radiation, it is generally avoided unless the diagnostic benefit outweighs the potential risk to the fetus or infant. Consultation with a radiologist and obstetrician is essential.

To order Metatrace Fdg, submit an enquiry on the product page at gnhindia.com specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including cold‑chain logistics if needed), and import documentation.

Metatrace Fdg is the standard FDG‑based tracer for assessing glucose metabolism, making it widely applicable across oncology, cardiology, and neurology. Alternative tracers such as 68Ga‑DOTATATE target specific receptors and are used for neuroendocrine tumors, but they do not provide the same broad metabolic information as FDG.

Metatrace Fdg should be stored refrigerated at 2–8 °C, protected from light, and kept in its original container. Do not freeze or shake the vial. Before use, allow the product to reach room temperature if required by the imaging protocol, and handle with radiation safety precautions.

Metatrace Fdg is administered as an intravenous injection by qualified nuclear medicine personnel. The dose is prepared in a sterile syringe and injected into a peripheral vein, after which the patient typically rests for a short uptake period before the PET scan begins.

Serious risks include allergic reactions that can progress to anaphylaxis, severe hypoglycemia especially in diabetic patients, and radiation‑related effects such as tissue injury or fetal exposure. Immediate medical attention is required if any severe reaction occurs.

Metatrace Fdg should be avoided in patients with uncontrolled hyperglycemia, known severe allergy to any component of the formulation, and in pregnant women unless the diagnostic benefit justifies the radiation risk. Patients with severe renal impairment should be evaluated carefully before use.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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