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 for intravenous use. It enables positron emission tomography (PET) imaging of dopaminergic neuronal activity and is employed in the diagnostic evaluation of Parkinson's disease and related neuroendocrine conditions.

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

Manufacturer / TM Owner

Curium Austria Gmbh

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Indications & Clinical Uses

Iasodopa is used to visualize dopaminergic pathways and assist in the diagnosis of movement and neuroendocrine disorders.

  • Parkinson's disease: provides quantitative PET imaging of striatal dopamine synthesis to support diagnosis and disease staging.
  • Neuroendocrine tumors: highlights somatostatin‑receptor positive lesions for accurate tumor localization.
  • Research studies: serves as a tracer for investigating brain dopamine metabolism in clinical and academic investigations.

How It Works

  • Fluorodopa (18F) is taken up by presynaptic dopaminergic neurons via the same transporters used for natural L‑DOPA. Inside the neuron it is enzymatically decarboxylated to fluorodopamine, which is stored in synaptic vesicles. The radioactive fluorine‑18 emits positrons that are detected by PET scanners, producing high‑resolution images of dopaminergic activity and allowing assessment of neuronal integrity.

Side Effects

Adverse reactions are generally mild and related to the radiopharmaceutical nature of the product.

Common Side Effects

  • Nausea: transient feeling of queasiness after injection.
  • Headache: mild to moderate discomfort lasting a short period.
  • Injection site pain: brief soreness at the venipuncture site.
  • Transient flushing: brief skin redness or warmth.
  • Mild dizziness: temporary light‑headedness.
  • Fatigue: short‑term tiredness post‑procedure.

Serious or Rare Side Effects

  • Allergic reaction: rash, itching, or anaphylaxis in susceptible individuals.
  • Radiation‑induced tissue injury: unlikely but possible with high cumulative exposure.
  • Severe hypotension: abrupt drop in blood pressure following administration.
  • Cardiac arrhythmia: rare disturbances in heart rhythm.
  • Acute renal impairment: potential impact on kidney function in vulnerable patients.
  • Neurotoxicity: extremely rare, related to excessive dopaminergic stimulation.

Precautions & Warnings

Prior to administration, clinicians should evaluate patient‑specific factors and follow radiation safety guidelines.

  • Pregnancy: avoid unless the diagnostic benefit outweighs potential fetal radiation risk.
  • Breastfeeding: discontinue breastfeeding for an appropriate interval after dosing.
  • Renal function: assess kidney performance, as impaired clearance may increase radiation exposure.
  • Concomitant PET tracers: schedule appropriately to prevent image interference.
  • Radiation safety: ensure staff and environment adhere to institutional radiation protection protocols.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Fluorodopa may interact with other agents that affect dopaminergic pathways or imaging quality.

Major Interactions (Avoid)

  • Concurrent radiopharmaceuticals: may cause overlapping signals and compromise image interpretation.
  • High‑dose dopamine agonists: can compete for neuronal uptake, reducing tracer accumulation.

Moderate Interactions (Monitor Closely)

  • Anticholinergic drugs: may alter dopaminergic signaling and affect tracer distribution.
  • MAO inhibitors: can modify dopamine metabolism, potentially influencing imaging results.
  • Contrast agents: may affect PET image quality if administered close in time.
  • Sedatives: may impact patient movement and image clarity.

Frequently Asked Questions

Iasodopa is a radiopharmaceutical used primarily for positron emission tomography (PET) imaging of dopaminergic neurons. It helps clinicians assess the integrity of the dopamine system in conditions such as Parkinson's disease and can also aid in locating certain neuroendocrine tumors.

Fluorodopa (18F) mimics the natural amino acid L‑DOPA and is transported into dopaminergic neurons. Inside the cell it is converted to fluorodopamine, which is stored in vesicles. The fluorine‑18 isotope emits positrons that are captured by PET scanners, producing detailed images of dopamine synthesis and storage.

The specific dose of Iasodopa is determined by the prescribing physician based on the patient’s weight, clinical indication, and the imaging protocol. Dosing is individualized and should follow the guidelines provided by the nuclear medicine department and the product’s prescribing information.

Fluorodopa involves exposure to ionizing radiation, so its use during pregnancy is generally avoided unless the diagnostic benefit clearly outweighs the potential risk to the fetus. Breastfeeding mothers should discontinue nursing for a period recommended by the treating physician to prevent radiation exposure to the infant.

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 handling if needed) and any required import documentation.

Iasodopa (18F‑fluorodopa) is a well‑established tracer that directly reflects dopamine synthesis, offering high specificity for dopaminergic neurons. Alternative tracers, such as 11C‑raclopride or 18F‑FDG, assess receptor binding or glucose metabolism respectively, which may provide complementary information but do not measure dopamine production as directly as fluorodopa.

Iasodopa must be stored at 2‑8 °C in its original container, protected from light, and should never be frozen or shaken. Because it is a short‑lived radiopharmaceutical, it is typically supplied just before use and must be handled by trained personnel in a controlled environment.

Iasodopa is administered intravenously by a qualified healthcare professional. The injection is given as a single bolus or slow infusion, depending on the imaging protocol, and is followed by a waiting period to allow tracer uptake before PET scanning begins.

The most serious risks include allergic reactions that can progress to anaphylaxis, radiation‑induced tissue injury with high cumulative exposure, severe hypotension, and rare neurotoxic effects. Patients should be monitored during and after administration, and appropriate emergency measures must be available.

Iasodopa should be avoided in patients with known hypersensitivity to fluorodopa or any component of the formulation, pregnant women unless absolutely necessary, and individuals with severe renal impairment where radiation exposure cannot be adequately cleared. Additionally, patients receiving competing radiopharmaceuticals within a short interval should defer Iasodopa administration.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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