GNH USA

Europe — EMA

Iodopol

GNH USA supplies Iodopol (Sodium Iodide I-131), a radioactive iodine for thyroid cancer, hyperthyroidism and thyroid imaging.

Sodium Iodide (131i)

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What is Sodium Iodide (131i)?

Sodium Iodide I-131, the active ingredient in Iodopol, is a radioactive iodine presented as an oral preparation for oral use. It treats thyroid disease such as thyroid cancer, hyperthyroidism, and is employed for thyroid tissue ablation and diagnostic imaging of the thyroid.

GNH USA supplies Iodopol 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?

Iodopol (Sodium Iodide I-131) is a radioactive iodine used in the management of thyroid disorders.

- Thyroid cancer: provides targeted radiation to destroy residual thyroid tissue after surgery. - Hyperthyroidism: ablates over‑active thyroid tissue to reduce hormone production. - Thyroid tissue ablation: prepares patients for subsequent radioactive iodine therapy or facilitates diagnostic imaging. - Diagnostic imaging of the thyroid: enables scintigraphic evaluation of thyroid function and anatomy.

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

Iodopol may cause a range of adverse reactions.

Common Side Effects: - Nausea or vomiting - Dry mouth or altered taste - Neck pain or tenderness - Transient hypothyroidism - Mild leukopenia or reduced blood counts - Fatigue or mild headache

Serious or Rare Side Effects: - Severe hypothyroidism requiring hormone replacement - Radiation thyroiditis with painful swelling - Bone marrow suppression leading to pancytopenia - Secondary malignancies such as leukemia - Allergic reactions including rash or anaphylaxis - Pulmonary fibrosis in rare cases

What precautions apply to Sodium Iodide (131i)?

Before using Iodopol, consider the following safety measures.

- Pregnancy: avoid unless clearly indicated, as fetal radiation exposure can be harmful. - Breastfeeding: discontinue nursing or choose an alternative, because iodine can be secreted in milk. - Radiation safety: limit close contact with pregnant women and young children for several days after administration. - Thyroid function monitoring: perform baseline and periodic thyroid hormone tests. - Hematologic monitoring: check complete blood counts before and after treatment. - Interference with other iodine‑containing drugs: suspend antithyroid medications and high‑dose iodinated contrast agents as advised. - Store at ambient temperature below 25°C: keep in the original pack, protect from moisture and direct sunlight.

What does Sodium Iodide (131i) interact with?

Iodopol can interact with several medicines and substances.

Major Interactions (Avoid): - Antithyroid drugs (e.g., propylthiouracil, methimazole) markedly reduce iodine uptake. - Lithium therapy diminishes thyroid iodine accumulation. - High‑dose iodinated contrast agents administered shortly before or after Iodopol can interfere with therapeutic efficacy.

Moderate Interactions (Monitor Closely): - Levothyroxine may require dose adjustment after Iodopol therapy. - Myelosuppressive chemotherapy agents can compound bone‑marrow toxicity. - Certain radiopharmaceuticals used for other diagnostic purposes may increase cumulative radiation exposure.

Frequently asked questions

What is Iodopol used for?+
Iodopol contains Sodium Iodide I-131 and is used to treat thyroid cancer, manage hyperthyroidism, ablate residual thyroid tissue, and provide diagnostic imaging of the thyroid gland. The radioactive iodine is selectively taken up by thyroid cells, allowing both therapeutic and imaging applications.
How does Sodium Iodide I-131 work?+
Sodium Iodide I-131 is absorbed by thyroid follicular cells via the sodium‑iodide symporter. Inside the cells, the isotope emits beta particles that destroy thyroid tissue, while gamma emissions enable external imaging. This dual action delivers localized radiation therapy and facilitates scintigraphic assessment.
What is the usual dose of Iodopol?+
The exact dose of Iodopol is determined by the prescribing physician based on the patient’s condition, thyroid size, and intended therapeutic goal. Dosing is individualized and may be expressed in megabecquerels (MBq) or millicuries (mCi) according to clinical guidelines.
Is Iodopol safe in pregnancy or breastfeeding?+
Iodopol is generally contraindicated during pregnancy because the radioactive iodine can affect the developing fetus. Breastfeeding should be discontinued before treatment, as iodine can be secreted in milk and expose the infant to radiation. Consultation with a specialist is essential if use is considered.
How do I order Iodopol from GNH USA?+
To order Iodopol, 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 any cold‑chain requirements), and necessary import documentation.
How does Iodopol compare with alternative treatments?+
Compared with non‑radioactive therapies such as antithyroid drugs or surgery, Iodopol offers a non‑invasive option that delivers targeted radiation directly to thyroid tissue. It can be more convenient than repeated surgeries and provides simultaneous therapeutic and diagnostic capabilities, though it requires careful radiation safety management.
How should Iodopol be stored and handled?+
Iodopol should be stored at ambient temperature below 25 °C, in its original container, protected from moisture and direct sunlight. Handling must follow radiation safety protocols, including the use of shielding and limiting exposure to others, especially pregnant women and children, for the period recommended by the prescriber.
How is Iodopol administered?+
Iodopol is administered orally as a single dose in capsule or liquid form, depending on the product presentation. The patient swallows the dose with water, and the medication is absorbed and concentrated by the thyroid gland. Administration is performed under medical supervision, often in a controlled clinical setting.
What are the most serious risks to watch for with Iodopol?+
Serious risks include severe hypothyroidism requiring lifelong hormone replacement, radiation thyroiditis with painful swelling, bone‑marrow suppression leading to pancytopenia, and the rare possibility of secondary malignancies such as leukemia. Patients should be monitored closely for these complications after treatment.
Who should not use Iodopol?+
Iodopol should be avoided in patients who are pregnant, breastfeeding, have uncontrolled severe hypothyroidism, or have a known hypersensitivity to iodine or radioactive substances. It is also contraindicated in individuals who have recently received high‑dose iodinated contrast agents or are on medications that block iodine uptake without appropriate medical guidance.
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
Narodowe Centrum Badań Jądrowych
Origin
EU

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