Product image of Iasodopa (Fluorodopa (18f)) supplied by GNH India

Iasodopa

Active Ingredient:
Fluorodopa (18f)
Origin:
EU

Iasodopa (Fluorodopa (18f))

Fluorodopa, the active ingredient in Iasodopa, is a radiopharmaceutical presented as an injectable solution for intravenous use. The tracer is incorporated into PET protocols to visualize presynaptic dopamine synthesis, providing clinicians with quantitative data for treatment planning. It is employed to evaluate Parkinsonian syndromes and assess dopaminergic function in the brain, aiding the differential diagnosis of movement disorders.

GNH India supplies Iasodopa as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, ensuring consistent quality and regulatory compliance across global markets.

Manufacturer / TM Owner

Curium Austria Gmbh

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Indications & Clinical Uses

Fluorodopa is employed as a PET radiotracer to visualize presynaptic dopamine synthesis, supporting the clinical assessment of disorders that affect the dopaminergic pathways.

  • Parkinsonian syndromes: enables PET imaging to assess presynaptic dopamine synthesis and storage.
  • Differential diagnosis of movement disorders: helps distinguish Parkinson's disease from other tremor or dystonia conditions.
  • Assessment of dopaminergic function in the brain: provides quantitative data on dopamine synthesis for clinical evaluation.
  • Clinical research of neurodegenerative diseases: allows measurement of dopamine pathway activity in investigational studies.

How It Works

  • Fluorodopa is L‑DOPA labeled with fluorine‑18. After intravenous injection it is transported into dopaminergic neurons via amino‑acid transporters and decarboxylated by aromatic L‑amino‑acid decarboxylase to fluorodopamine. The radiolabelled metabolite is trapped in presynaptic terminals, enabling PET scanners to image and quantify dopamine synthesis and storage in the brain.

Side Effects

Fluorodopa may be associated with adverse reactions related to its radiopharmaceutical nature and intravenous administration.

Common Side Effects

  • Nausea: mild to moderate nausea reported after injection.
  • Headache: transient headache may occur.
  • Injection site discomfort: mild pain or erythema at the infusion site.
  • Transient hypotension: brief drop in blood pressure in some patients.
  • Flushing: temporary skin flushing observed in a minority of subjects.

Serious or Rare Side Effects

  • Allergic reaction: anaphylaxis or severe hypersensitivity.
  • Radiation‑induced tissue injury: rare localized tissue effects from radiation exposure.
  • Severe hypotension: prolonged low blood pressure requiring intervention.
  • Nephrotoxicity: rare kidney function impairment.
  • Cardiac arrhythmia: rare occurrence of rhythm disturbances.

Precautions & Warnings

When using Fluorodopa, consider the following precautions to ensure patient safety and product integrity.

  • Pregnancy: use only if clearly needed, as fetal radiation exposure is unknown.
  • Breastfeeding: avoid breastfeeding for a period after administration due to possible radiotracer excretion.
  • Renal impairment: assess kidney function before dosing, as clearance may be reduced.
  • Concomitant medications: evaluate drugs affecting dopamine metabolism, such as carbidopa, which may alter tracer uptake.
  • Patient monitoring: observe vital signs and for allergic reactions during and after injection.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Fluorodopa can interact with certain substances that affect dopamine pathways or radiotracer distribution.

Major Interactions (Avoid)

  • Carbidopa or benserazide: potent inhibition of aromatic L‑amino acid decarboxylase reduces tracer conversion, compromising imaging.
  • Antipsychotics (e.g., haloperidol, risperidone): block dopamine receptors and may alter tracer uptake, affecting diagnostic accuracy.

Moderate Interactions (Monitor Closely)

  • MAO‑B inhibitors (e.g., selegiline): may increase fluorodopamine levels, potentially affecting image interpretation.
  • Antidepressants influencing dopamine (e.g., bupropion): could modify tracer distribution.
  • High‑dose levodopa therapy: competing substrate may reduce fluorodopa uptake.

Frequently Asked Questions

Iasodopa contains Fluorodopa, a radiopharmaceutical used in PET imaging to evaluate Parkinsonian syndromes and assess dopaminergic function in the brain, aiding the differential diagnosis of movement disorders.

Fluorodopa is L‑DOPA labeled with fluorine‑18. After intravenous injection it enters dopaminergic neurons, where it is decarboxylated to fluorodopamine. The radioactive label allows PET scanners to visualize and quantify presynaptic dopamine synthesis and storage.

The administered activity of Fluorodopa is determined by the prescribing nuclear medicine physician based on patient weight, scanner sensitivity, and regulatory guidelines. The prescriber sets the exact dose and timing for each examination.

The safety of Fluorodopa during pregnancy and lactation has not been established. Use is only considered when the diagnostic benefit outweighs potential fetal or infant radiation exposure, and appropriate precautions should be taken.

To place an order, 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 if needed) and necessary import documentation.

The primary alternative is 18F‑FDOPA versus other PET tracers such as 123I‑FP‑CIT (SPECT) or 11C‑raclopride. Fluorodopa offers direct measurement of dopamine synthesis, providing higher specificity for presynaptic function, whereas other agents may assess dopamine transporter density or receptor binding.

Iasodopa must be stored refrigerated at 2‑8 °C, protected from light, and kept in its original container. Do not freeze or agitate the vial, and use the product within the shelf‑life indicated by the manufacturer.

Iasodopa is supplied as a sterile injectable solution for intravenous infusion. The radiotracer is administered by a qualified nuclear medicine professional, typically as a rapid bolus or short infusion, followed by a waiting period before PET imaging commences.

Serious adverse events include allergic reactions such as anaphylaxis, significant hypotension, and rare radiation‑induced tissue injury. Patients should be monitored closely during and after injection for any signs of hypersensitivity or hemodynamic changes.

Iasodopa is contraindicated in patients with known hypersensitivity to Fluorodopa or any component of the formulation, and should be avoided in individuals where the diagnostic benefit does not outweigh the potential radiation risk, such as pregnant women without a clear indication.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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