GNH USA

Europe — EMA

Ioduro (131i) De Sodio Ge Healthcare

GNH USA supplies Ioduro (131i) De Sodio (Sodium Iodide), a radioactive iodine for thyroid imaging, cancer treatment and hyperthyroidism.

Sodium Iodide (131i)

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What is Sodium Iodide (131i)?

Sodium Iodide (131I), the active ingredient in Ioduro (131i) De Sodio, is a radioactive iodine presented as an oral solution for oral use. It is used in the diagnosis and treatment of thyroid disorders, including imaging, cancer therapy, and hyperthyroidism.

GNH USA supplies Ioduro (131i) De Sodio as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

What is Sodium Iodide (131i) used for?

Ioduro (Sodium Iodide 131I) is employed in the thyroid pathway for both diagnostic and therapeutic purposes.

Thyroid imaging: Enables visualization of thyroid tissue using radioactive uptake for diagnostic scans. Thyroid cancer treatment: Delivers targeted radiation to thyroid carcinoma cells to reduce tumor burden. Hyperthyroidism: Provides therapeutic radiation to suppress overactive thyroid tissue.

What are the side effects of Sodium Iodide (131i)?

Adverse reactions may occur following oral administration of radioactive iodine.

Common Side Effects: - Nausea or vomiting - Altered taste sensation - Mild salivary gland discomfort - Transient fatigue - Temporary hypothyroidism - Mild headache

Serious or Rare Side Effects: - Severe hypothyroidism requiring hormone replacement - Radiation thyroiditis - Bone marrow suppression - Allergic reactions such as rash or anaphylaxis - Radiation‑induced sialadenitis - Rare secondary malignancies

What precautions apply to Sodium Iodide (131i)?

Use of Ioduro requires careful consideration of patient‑specific factors and handling requirements.

Pregnancy: Use only if clearly needed; potential fetal radiation exposure. Breastfeeding: Contraindicated; iodine may be secreted in milk. Renal impairment: Adjust dose; reduced clearance may increase systemic exposure. Thyroid function: Baseline assessment required before administration. Drug interactions: Avoid concurrent high‑iodine substances. Store at ambient temperature: Keep below 25°C, in the original container, protected from moisture and light.

What does Sodium Iodide (131i) interact with?

Ioduro may interact with other medications that affect iodine handling or thyroid function.

Major Interactions (Avoid): - Antithyroid drugs (e.g., propylthiouracil, methimazole): May reduce uptake of radioactive iodine. - High‑iodine contrast agents: Can block thyroid uptake of I‑131. - Lithium carbonate: Increases retention of iodine in the thyroid, altering therapeutic effect.

Moderate Interactions (Monitor Closely): - Amiodarone: Contains iodine and may affect dosing. - Corticosteroids: May modify inflammatory response after therapy. - Diuretics: May affect renal clearance of iodine.

Frequently asked questions

What is Ioduro (131i) De Sodio used for?+
Ioduro (131i) De Sodio, containing Sodium Iodide (131I), is used for thyroid imaging, treatment of thyroid cancer, and management of hyperthyroidism. The radioactive iodine is taken up by thyroid tissue, allowing clinicians to visualize the gland or deliver localized radiation to abnormal cells.
How does Sodium Iodide (131I) work?+
Sodium Iodide (131I) is absorbed by thyroid cells via the sodium‑iodide symporter. Once inside, the isotope emits beta particles that either generate images for diagnostic scans or provide therapeutic radiation that destroys overactive or malignant thyroid tissue while sparing most surrounding structures.
What is the usual dose of Ioduro (131i) De Sodio?+
The dose of Ioduro (131i) De Sodio is individualized and determined by the prescribing physician based on the specific indication, patient weight, thyroid function, and treatment goals. No standard dosing can be provided without a medical assessment.
Is Ioduro safe during pregnancy or breastfeeding?+
Radioactive iodine can cross the placenta and be secreted in breast milk, posing potential risks to the fetus or infant. Use during pregnancy or lactation is only considered when the benefit outweighs the risk and should be guided by a specialist.
How do I order Ioduro (131i) De Sodio from GNH USA?+
To order, submit an enquiry on the product page at gnh-usa.com indicating 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 any cold‑chain needs) and import documentation.
How does Ioduro compare with other radioactive iodine products?+
Ioduro delivers Sodium Iodide (131I) in an oral solution, similar to other I‑131 preparations. Differences may lie in formulation purity, regulatory approvals, and supply chain reliability. Clinicians choose based on local licensing, dosing flexibility, and the supplier’s ability to meet quality and delivery standards.
What are the storage and handling requirements for Ioduro?+
Ioduro should be stored at ambient temperature, preferably below 25 °C, in its original sealed container. Protect the solution from moisture, direct sunlight, and physical damage. Follow local regulations for handling radioactive materials and keep it out of reach of unauthorized personnel.
How is Ioduro administered?+
Ioduro is administered orally as a measured volume of solution. The patient drinks the dose under medical supervision, often after fasting or following specific preparation instructions to optimize thyroid uptake. Administration details are provided by the treating physician.
What are the most serious risks to watch for with Ioduro?+
Serious risks include severe hypothyroidism, radiation thyroiditis, bone‑marrow suppression, allergic reactions, and, rarely, secondary malignancies. Patients should be monitored for signs of these events, and any sudden symptoms such as fever, unexplained bruising, or severe neck pain should prompt immediate medical evaluation.
Who should not use Ioduro (131i) De Sodio?+
Ioduro is contraindicated in pregnant or breastfeeding women unless absolutely necessary, individuals with known hypersensitivity to iodine or radioactive compounds, and patients with uncontrolled severe renal impairment where clearance cannot be assured. A thorough clinical assessment is required before use.
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 (131i)
Route
Oral Use
Manufacturer
Ge Healthcare Bio-Sciences, S.A.U.
Origin
EU

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