Product image of Natrii Iodidum (131i) Polatom (Sodium Iodide (131i)) supplied by GNH India

Natrii Iodidum (131i) Polatom

Active Ingredient:
Sodium Iodide (131i)
Origin:
EU

Natrii Iodidum (131i) Polatom (Sodium Iodide (131i))

Sodium Iodide (I-131), the active ingredient in Natrii Iodidum (131i) Polatom, is a radiopharmaceutical presented as an oral preparation for oral use. It is employed to treat hyperthyroidism, manage thyroid cancer, and to achieve thyroid tissue ablation or diagnostic imaging of thyroid function.

GNH India supplies Natrii Iodidum (131i) Polatom as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Narodowe Centrum Badań Jądrowych

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Indications & Clinical Uses

Natrii Iodidum (131i) Polatom is a radioactive iodine agent used in the management of thyroid‑related disorders and imaging.

  • Hyperthyroidism: reduces excess thyroid hormone production by selectively destroying overactive thyroid cells.
  • Thyroid cancer: eliminates residual thyroid tissue after surgery to lower recurrence risk.
  • Thyroid tissue ablation: prepares patients for subsequent radioiodine therapy by ablating remaining thyroid tissue.
  • Diagnostic thyroid imaging: provides functional imaging to assess thyroid uptake and distribution.

How It Works

  • Sodium Iodide (I-131) is actively taken up by thyroid follicular cells via the sodium‑iodide symporter. Once inside the gland, the beta particles emitted by I‑131 cause localized radiation injury, leading to selective destruction of thyroid tissue while sparing surrounding structures. This targeted cytotoxic effect underlies both therapeutic ablation and diagnostic imaging applications.

Side Effects

Adverse reactions may occur following oral administration of I‑131 radiopharmaceuticals.

Common Side Effects

  • Nausea or vomiting
  • Transient neck discomfort or soreness
  • Mild hypothyroidism during the first weeks
  • Altered taste sensation
  • Temporary leukopenia or mild bone‑marrow suppression
  • Mild salivary gland irritation

Serious or Rare Side Effects

  • Severe or prolonged hypothyroidism requiring hormone replacement
  • Acute radiation thyroiditis with significant pain and swelling
  • Bone‑marrow failure leading to pancytopenia
  • Allergic or hypersensitivity reactions, including rash or anaphylaxis
  • Pulmonary fibrosis (rare) from systemic radiation exposure
  • Secondary malignancies due to radiation exposure (very rare)

Precautions & Warnings

Careful assessment and monitoring are required when using I‑131 radiopharmaceuticals.

  • Pregnancy: avoid use unless the benefit outweighs the risk to the fetus.
  • Breastfeeding: discontinue treatment and advise cessation of nursing until radioactivity is cleared.
  • Renal impairment: monitor renal function and adjust timing of administration as needed.
  • Concomitant thyroid hormone therapy: closely monitor thyroid hormone levels and adjust dosage.
  • Radiation safety: implement measures to limit exposure to family members and healthcare staff.
  • Store at ambient temperature: keep in original packaging, protect from moisture and light, and store below 25 °C.

Avoid Interactions

I‑131 may interact with other medications that affect thyroid function or radiation response.

Major Interactions (Avoid)

  • Antithyroid drugs (e.g., propylthiouracil, methimazole) can reduce iodine uptake.
  • Lithium therapy may alter thyroid hormone dynamics and increase risk of hypothyroidism.
  • High‑dose iodine supplements or contrast agents can competitively inhibit I‑131 uptake.
  • Radioprotective agents such as amifostine may diminish therapeutic efficacy.
  • Concurrent chemotherapy causing bone‑marrow suppression may exacerbate hematologic toxicity.

Moderate Interactions (Monitor Closely)

  • Levothyroxine replacement: adjust dose based on thyroid function tests.
  • Corticosteroids: may mask inflammatory responses.
  • Anticoagulants: monitor for bleeding if thyroiditis occurs.
  • Diuretics: watch for electrolyte disturbances during thyroid inflammation.
  • Antihistamines: may affect perception of mild allergic reactions.

Frequently Asked Questions

Natrii Iodidum (131i) Polatom contains sodium iodide labeled with iodine‑131 and is used to treat hyperthyroidism, to ablate residual thyroid tissue after surgery for thyroid cancer, and for diagnostic imaging of thyroid function. It works by delivering targeted radiation to thyroid cells.

Sodium iodide (I-131) is taken up by thyroid cells via the sodium‑iodide symporter. Once inside, the beta radiation emitted by I‑131 damages cellular DNA, leading to selective destruction of thyroid tissue while sparing most other tissues. This mechanism provides both therapeutic and imaging capabilities.

The dose of Natrii Iodidum (131i) Polatom is determined by the prescribing physician based on the specific indication, patient weight, thyroid uptake studies, and clinical response. Only a qualified healthcare professional should set the appropriate activity for each patient.

Use during pregnancy is generally avoided because the radioactive iodine can cross the placenta and affect the fetal thyroid. Breastfeeding should be discontinued during and after treatment until the radioactivity has cleared, as I‑131 can be secreted in breast milk.

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 any cold‑chain requirements) and necessary import documentation.

Compared with non‑radioactive antithyroid drugs, I‑131 provides a one‑time definitive therapy that permanently reduces thyroid tissue. Unlike external beam radiation, oral I‑131 delivers targeted internal radiation with minimal exposure to surrounding structures, making it a preferred option for many cases of hyperthyroidism and post‑surgical thyroid cancer management.

The product should be stored at ambient temperature, below 25 °C, in its original container. Protect it from moisture, direct sunlight, and physical damage. Follow all local regulations for handling radioactive materials, including using appropriate shielding and labeling.

Natrii Iodidum (131i) Polatom is administered orally as a single dose under medical supervision. The patient swallows the tablet or capsule with water, and thyroid uptake is typically assessed with a scan to confirm appropriate absorption before proceeding.

Serious risks include severe hypothyroidism requiring lifelong hormone replacement, acute radiation thyroiditis, bone‑marrow suppression leading to cytopenias, allergic reactions, and, rarely, secondary malignancies due to radiation exposure. Patients should be monitored closely for these events.

Patients who are pregnant, breastfeeding, have uncontrolled severe renal impairment, or have a known hypersensitivity to iodine‑131 should avoid this product. Additionally, individuals who cannot comply with radiation safety precautions or who have active infections that could be worsened by immunosuppression should not receive it.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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