Product image of Mibg (123i) Curium Netherlands (Iodine (123i) Iobenguane) supplied by GNH India

Mibg (123i) Curium Netherlands

Active Ingredient:
Iodine (123i) Iobenguane
Origin:
EU

Mibg (123i) Curium Netherlands (Iodine (123i) Iobenguane)

Iobenguane (I-123), the active ingredient in Mibg (123i) Curium Netherlands, is a radiopharmaceutical presented as an injectable radiopharmaceutical for intravenous use. It is employed in nuclear medicine to visualize sympathetic nerve activity for diagnostic purposes in selected patient groups.
GNH India supplies Mibg (123i) Curium Netherlands as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

Curium Netherlands B.V.

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Indications & Clinical Uses

Iobenguane (I-123) is used in nuclear‑medicine procedures that assess sympathetic innervation and catecholamine‑producing tumors.

  • Myocardial innervation imaging: visualizes cardiac sympathetic nerve distribution to evaluate autonomic function.
  • Pheochromocytoma detection: highlights catecholamine‑secreting adrenal tumors for accurate localization.
  • Neuroblastoma imaging: identifies sympathetic‑origin pediatric tumors and assesses disease extent.

How It Works

  • Iobenguane (I‑123) mimics norepinephrine and is taken up by adrenergic nerve terminals via the norepinephrine transporter. Once internalized, the radio‑iodine emits gamma photons that are captured by a gamma camera, allowing three‑dimensional visualization of sympathetic innervation and catecholamine‑producing lesions during nuclear imaging.

Side Effects

Adverse reactions are generally mild but can occur after intravenous administration.

Common Side Effects

  • Injection site pain or erythema
  • Nausea or mild vomiting
  • Transient headache
  • Flushing or warmth sensation
  • Mild hypotension
  • Dizziness or light‑headedness

Serious or Rare Side Effects

  • Anaphylactic or severe allergic reaction
  • Significant hypotension requiring intervention
  • Radiation‑induced thyroid dysfunction
  • Bone‑marrow suppression with prolonged exposure
  • Severe arrhythmias in patients with underlying cardiac disease
  • Acute renal impairment in susceptible individuals

Precautions & Warnings

Prior to use, clinicians should evaluate patient‑specific factors that may affect safety or image quality.

  • Pregnancy: avoid unless the diagnostic benefit outweighs fetal radiation risk.
  • Breastfeeding: discontinue nursing for an appropriate interval after administration.
  • Thyroid blocking: consider potassium iodide pretreatment to reduce thyroid uptake of free iodine.
  • Renal function: assess because the tracer is excreted renally and impaired function may increase radiation exposure.
  • Concomitant norepinephrine‑modulating drugs: may alter tracer distribution and affect image interpretation.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

Iobenguane (I‑123) may have interactions that influence tracer uptake or patient safety.

Major Interactions (Avoid)

  • Thyroid blocking agents (e.g., potassium iodide) that compete for iodine uptake and reduce image quality.
  • Strong norepinephrine transporter inhibitors (e.g., reserpine, certain antidepressants) that markedly diminish tracer accumulation.
  • High‑dose radiopharmaceuticals administered within 24 hours, which can increase cumulative radiation dose.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may blunt heart‑rate response during cardiac imaging.
  • Calcium‑channel blockers: can modestly affect myocardial perfusion patterns.
  • Other diagnostic radiotracers given in close succession: may cause cross‑interference on imaging results.

Frequently Asked Questions

Iobenguane (I‑123) is a radiopharmaceutical used in nuclear‑medicine scans to visualize sympathetic nerve activity. It helps assess cardiac autonomic innervation, locate catecholamine‑producing tumors such as pheochromocytoma, and detect neuroblastoma lesions in children.

The compound mimics norepinephrine and is taken up by nerve terminals via the norepinephrine transporter. Once inside the cells, the I‑123 isotope emits gamma photons that are captured by a gamma camera, producing detailed images of sympathetic innervation and tumor sites.

The administered activity is determined by the prescribing physician or nuclear medicine specialist based on the specific diagnostic protocol, patient weight, and the imaging equipment used. Dosage is individualized and not standardized across all patients.

Iobenguane (I‑123) involves ionizing radiation, so it is generally avoided in pregnancy unless the diagnostic benefit clearly outweighs the potential fetal risk. 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 if needed), and necessary import documentation.

Compared with non‑radioactive imaging modalities, Iobenguane (I‑123) offers high‑resolution functional imaging of sympathetic nerves. Unlike other radiotracers such as 123I‑MIBG, it provides similar diagnostic information but may differ in pharmacokinetics and availability depending on regional regulatory approvals.

The product should be stored refrigerated at 2‑8 °C, protected from light, and never frozen or shaken. It must be handled in a controlled‑radiation environment by trained personnel, using appropriate shielding and waste disposal procedures.

Iobenguane (I‑123) is administered intravenously by a qualified healthcare professional. The injection is typically performed in a nuclear medicine suite, followed by a waiting period to allow tracer distribution before imaging with a gamma camera.

Serious risks include severe allergic reactions, significant hypotension, radiation‑induced thyroid dysfunction, and, in rare cases, bone‑marrow suppression. Patients should be monitored closely during and after administration, especially if they have pre‑existing cardiac or thyroid conditions.

Patients with known hypersensitivity to iodine‑based compounds, uncontrolled hypertension, severe cardiac arrhythmias, or those who are pregnant or breastfeeding without a compelling diagnostic need should not receive Iobenguane (I‑123). Clinical judgment is essential to determine suitability.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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