GNH USA

Europe — EMA

Ioduro (123i) De Sodio Ge Healthcare

GNH USA supplies Ioduro (123i) De Sodio (Sodium Iodide), a radioactive diagnostic agent for thyroid imaging and related studies.

Sodium Iodide (123 I)

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What is Sodium Iodide (123 I)?

Sodium Iodide, the active ingredient in Ioduro (123i) De Sodio Ge Healthcare, is a radioactive diagnostic agent presented as a sterile solution for intravenous use. It is employed in nuclear medicine to image thyroid function and to locate iodine‑avid tissues in patients. GNH USA supplies Ioduro (123i) De Sodio Ge Healthcare as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

What is Sodium Iodide (123 I) used for?

Ioduro (Sodium Iodide‑123) is used in nuclear medicine procedures that target iodine‑handling tissues. - Thyroid imaging: provides high‑resolution scintigraphy for assessment of thyroid function and morphology. - Detection of ectopic thyroid tissue: helps locate residual or ectopic thyroid tissue after surgery or in congenital cases. - Evaluation of pheochromocytoma: used in specific protocols to image catecholamine‑producing tumors that concentrate iodine.

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

Common Side Effects: - Nausea: mild, transient discomfort after injection. - Vomiting: occasional, usually self‑limiting. - Headache: mild to moderate, often resolves spontaneously. - Injection site pain: brief discomfort at the venipuncture site. - Transient taste alteration: metallic or iodine taste lasting minutes. - Mild flushing: temporary skin redness.

Serious or Rare Side Effects: - Severe allergic reaction (anaphylaxis): rare but requires immediate medical attention. - Thyrotoxicosis: excessive thyroid hormone release in susceptible individuals. - Radiation‑induced thyroiditis: inflammation of the thyroid gland. - Pulmonary edema: extremely rare, associated with high‑dose exposure. - Severe hypotension: sudden drop in blood pressure post‑administration.

What precautions apply to Sodium Iodide (123 I)?

Ioduro (Sodium Iodide‑123) should be used with careful clinical assessment and adherence to radiation safety guidelines. - Pregnancy: avoid unless essential, as fetal thyroid uptake may occur. - Breastfeeding: contraindicated; iodine can be secreted in breast milk. - Thyroid disorders: evaluate baseline thyroid function before administration. - Renal impairment: monitor renal function, as clearance may be reduced. - Allergy to iodine: contraindicated in patients with known hypersensitivity. - Radiation safety: employ appropriate shielding and limit exposure time for staff. - Store at 2-8°C: keep refrigerated, protect from light, do not freeze.

What does Sodium Iodide (123 I) interact with?

Ioduro (Sodium Iodide‑123) may interact with drugs that affect thyroid iodine handling or imaging quality. Major Interactions (Avoid): - Antithyroid drugs (e.g., methimazole, propylthiouracil): reduce iodine uptake, compromising image quality. - Lithium therapy: alters thyroid iodine transport, potentially affecting results. - High‑dose iodine supplements: compete for uptake, leading to false‑negative scans. Moderate Interactions (Monitor Closely): - Thyroid hormone replacement: may modify baseline activity, requiring dose adjustment of the radiopharmaceutical. - Contrast agents (iodinated): can transiently block iodine uptake; schedule imaging accordingly. - Beta‑blockers: may mask symptoms of adverse reactions such as tachycardia.

Frequently asked questions

What is Ioduro (123i) De Sodio used for?+
Ioduro (123i) De Sodio contains Sodium Iodide‑123, a radioactive diagnostic agent used in nuclear medicine to produce high‑resolution images of the thyroid gland and other iodine‑avid tissues. It helps clinicians assess thyroid function, locate ectopic thyroid tissue, and evaluate certain neuroendocrine tumors.
How does Sodium Iodide‑123 work in the body?+
Sodium Iodide‑123 is taken up by cells that express the sodium‑iodide symporter, especially thyroid follicular cells. Once inside the cells, the gamma‑emitting iodine‑123 provides a detectable signal for a gamma camera, allowing physicians to visualize the distribution and activity of iodine‑handling tissues without delivering a therapeutic radiation dose.
What is the usual dose of Ioduro (123i) De Sodio?+
The specific dose of Ioduro (123i) De Sodio is determined by the prescribing physician based on the diagnostic protocol, patient weight, and clinical indication. Dosage decisions are individualized and should follow the guidelines of the nuclear medicine department and the product’s prescribing information.
Is Sodium Iodide‑123 safe during pregnancy or breastfeeding?+
Sodium Iodide‑123 is generally avoided in pregnancy unless the diagnostic benefit outweighs the potential risk to the fetus, as the fetal thyroid can accumulate iodine. It is contraindicated during breastfeeding because iodine can be secreted in breast milk, potentially exposing the infant.
How do I order Ioduro (123i) De Sodio from GNH USA?+
To order, submit an enquiry on the product page at gnh-usa.com, providing the required quantity and your institutional credentials. GNH USA supplies hospitals, pharmacies, and procurement teams worldwide, and will respond with pricing, availability, shipping details (including any cold‑chain requirements), and the necessary import documentation.
How does Ioduro compare with other thyroid imaging agents?+
Ioduro (Sodium Iodide‑123) offers superior image quality and lower radiation dose compared with Iodine‑131, which is primarily therapeutic. Compared with Technetium‑99m pertechnetate, Sodium Iodide‑123 provides better quantitative assessment of thyroid uptake because it is actively transported via the sodium‑iodide symporter.
What are the storage and handling requirements for Ioduro?+
Ioduro should be stored at 2‑8 °C in its original sealed container, protected from light, and must not be frozen or shaken. Handling should be performed in a controlled environment with appropriate radiation safety measures to protect personnel.
How is Ioduro administered to patients?+
Ioduro is administered intravenously by a qualified healthcare professional. The injection is typically given as a single dose, after which the patient may be positioned for imaging using a gamma camera at the appropriate time interval dictated by the imaging protocol.
What are the most serious risks associated with Sodium Iodide‑123?+
The most serious risks include severe allergic reactions (anaphylaxis), radiation‑induced thyroiditis, and, in rare cases, thyrotoxicosis or pulmonary edema. Patients should be monitored for any signs of hypersensitivity or unexpected thyroid hormone changes following administration.
Who should not receive Ioduro (Sodium Iodide‑123)?+
Ioduro should not be given to patients with known iodine allergy, pregnant or breastfeeding women unless the diagnostic benefit justifies the risk, and individuals with uncontrolled thyroid disorders where iodine uptake could exacerbate the condition. Clinical judgment is essential to determine suitability.
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
Ge Healthcare Bio-Sciences, S.A.U.
Origin
EU

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