GNH USA

Europe — EMA

Iodure (123i) De Sodium Curiumpharma

GNH USA supplies Iodure (123i) De Sodium Curiumpharma (Sodium Iodide), a radiopharmaceutical for thyroid imaging and function evaluation.

Sodium Iodide (123 I)

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What is Sodium Iodide (123 I)?

Sodium Iodide, the active ingredient in Iodure (123i) De Sodium Curiumpharma, is a radiopharmaceutical presented as a sterile solution for intravenous use. It is used for diagnostic imaging of the thyroid and related tissues in patients requiring functional assessment.

GNH USA supplies Iodure (123i) De Sodium Curiumpharma as a licensed, GDP-compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres and pharmacies worldwide.

What is Sodium Iodide (123 I) used for?

Iodure (Sodium Iodide I‑123) is employed in nuclear medicine to visualize thyroid tissue and assess its function.

- Thyroid imaging: Provides high‑resolution scintigraphic images of thyroid anatomy and iodine uptake. - Evaluation of thyroid function: Quantifies glandular activity to differentiate hyper‑ and hypothyroidism. - Detection of thyroid cancer metastases: Identifies metastatic lesions by highlighting iodine‑avid tissue beyond the thyroid gland.

What are the side effects of Sodium Iodide (123 I)?

Adverse reactions may occur following intravenous administration of Iodure.

Common Side Effects: - Nausea: mild, transient feeling of stomach upset. - Headache: mild to moderate, usually resolves spontaneously. - Warmth or flushing: brief sensation at the injection site. - Injection site discomfort: mild pain or irritation. - Transient hypotension: slight drop in blood pressure shortly after dosing.

Serious or Rare Side Effects: - Allergic reaction: rash, itching, or anaphylaxis requiring immediate medical attention. - Severe hypotension: marked blood pressure decrease needing intervention. - Radiation‑induced thyroiditis: inflammation of the thyroid gland. - Hematologic abnormalities: rare changes in blood counts. - Pulmonary embolism: extremely rare, presenting with respiratory distress.

What precautions apply to Sodium Iodide (123 I)?

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

- Pregnancy: use only if the diagnostic benefit outweighs potential fetal radiation exposure. - Breastfeeding: consider temporary cessation of nursing or assess infant risk. - Renal function: assess because impaired clearance may affect radiation dose. - Thyroid status: avoid in untreated hyperthyroidism unless specifically indicated. - Radiation safety: adhere to institutional protocols for handling and disposal of radioactive material. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

What does Sodium Iodide (123 I) interact with?

Sodium Iodide I‑123 may interact with other agents that affect iodine metabolism or cardiovascular stability.

Major Interactions (Avoid): - Iodine‑containing contrast agents: can interfere with tracer uptake and imaging interpretation. - Thyroid hormone therapy: may alter iodine uptake, reducing diagnostic accuracy. - Antithyroid drugs: can diminish tracer accumulation in the thyroid.

Moderate Interactions (Monitor Closely): - Beta‑blockers: may blunt heart‑rate response during stress testing. - ACE inhibitors: monitor blood pressure for additive hypotensive effects. - Diuretics: observe fluid balance and renal function during administration.

Frequently asked questions

What is Iodure (123i) used for?+
Iodure (123i) contains Sodium Iodide I‑123 and is used as a diagnostic radiopharmaceutical for thyroid imaging, evaluation of thyroid function, and detection of metastatic thyroid cancer. The tracer is administered intravenously and imaged with a gamma camera to provide functional information about iodine‑avid tissues.
How does Sodium Iodide (I‑123) work in the body?+
Sodium Iodide I‑123 is actively transported into thyroid follicular cells by the sodium‑iodide symporter. Once inside, the radionuclide emits gamma radiation that is captured by a gamma camera, producing images that reflect the distribution and activity of thyroid tissue without significantly affecting hormone production.
What is the usual dose of Iodure (123i)?+
The administered activity of Iodure (123i) is determined by the prescribing physician based on the patient’s age, weight, clinical indication, and imaging protocol. Dosage is individualized and should follow local nuclear medicine guidelines and regulatory requirements.
Is Iodure (123i) safe during pregnancy or breastfeeding?+
Pregnancy and breastfeeding are considered relative contraindications because the radiotracer delivers ionising radiation. Use is permitted only when the diagnostic benefit outweighs potential risks to the fetus or infant, and appropriate radiation safety measures should be applied.
How do I order Iodure (123i) from GNH USA?+
To place an order, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA 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 import documentation.
How does Iodure (123i) compare with other thyroid imaging agents?+
Iodure (123i) uses I‑123, which emits gamma photons ideal for high‑resolution imaging and has a shorter half‑life than I‑131, resulting in lower radiation dose. Compared with technetium‑99m pertechnetate, I‑123 provides better thyroid uptake specificity, making it preferred for detailed functional studies.
What are the storage and handling requirements for Iodure (123i)?+
Iodure (123i) must be stored refrigerated at 2‑8 °C, protected from light, and should never be frozen or shaken. The product should be kept in its original container until use and handled in accordance with radiopharmaceutical safety protocols.
How is Iodure (123i) administered?+
The radiopharmaceutical is administered intravenously by a qualified healthcare professional. The injection is typically performed in a controlled nuclear medicine suite, and imaging is conducted shortly after administration according to the prescribed protocol.
What are the most serious risks associated with Iodure (123i)?+
Serious risks include allergic reactions ranging from rash to anaphylaxis, severe hypotension, radiation‑induced thyroiditis, and rare hematologic abnormalities. Patients should be monitored during and after injection, and any adverse signs should be addressed promptly.
Who should not receive Iodure (123i)?+
Patients with known hypersensitivity to iodine or radiopharmaceutical components, untreated hyperthyroidism (unless specifically indicated), pregnant or breastfeeding women where the benefit does not outweigh risk, and individuals unable to comply with radiation safety measures should not receive Iodure (123i).
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Sodium Iodide (123 I)
Route
Intravenous Use
Manufacturer
Curium Netherlands B.V.
Origin
EU

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