Product image of Jodek Sodu Na131i Polatom (Sodium Iodide (131i)) supplied by GNH India

Jodek Sodu Na131i Polatom

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

Jodek Sodu Na131i Polatom (Sodium Iodide (131i))

Sodium Iodide, the active ingredient in Jodek Sodu Na131i Polatom, is a radioactive iodine presented as a N/A/oral preparation for oral use. It is used for thyroid imaging, treatment of hyperthyroidism, and therapy of thyroid cancer in appropriate patients.

GNH India supplies Jodek Sodu Na131i Polatom as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, transplant centres, oncology centres, pharmacies and clinics worldwide, sourced from the European Union market.

Manufacturer / TM Owner

Narodowe Centrum Badań Jądrowych

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Indications & Clinical Uses

  • Sodium Iodide (Na131I) is employed in thyroid‑related diagnostic and therapeutic pathways.
  • Thyroid imaging: enables high‑resolution scintigraphy for accurate assessment of thyroid anatomy and function.
  • Hyperthyroidism treatment: delivers targeted radiation to reduce overactive thyroid tissue.
  • Thyroid cancer therapy: provides ablative radiation to eliminate residual or metastatic thyroid carcinoma cells.

How It Works

  • Sodium Iodide (Na131I) is taken up preferentially by thyroid follicular cells via the sodium‑iodide symporter. The radioactive iodine emits beta particles that cause localized cellular damage, while gamma emissions allow imaging. This selective uptake delivers therapeutic radiation to thyroid tissue while sparing most surrounding structures, enabling both diagnostic visualization and therapeutic ablation.

Side Effects

Sodium Iodide (Na131I) may be associated with a range of adverse reactions, varying from mild to serious.

Common Side Effects

  • Nausea or vomiting
  • Metallic taste in the mouth
  • Salivary gland swelling or discomfort
  • Mild headache or fatigue

Serious or Rare Side Effects

  • Severe hypothyroidism requiring hormone replacement
  • Bone marrow suppression leading to cytopenias
  • Allergic reactions such as rash, angioedema, or anaphylaxis

Precautions & Warnings

  • Sodium Iodide (Na131I) requires careful patient assessment and monitoring.
  • Pregnancy: avoid unless benefits outweigh risks.
  • Breastfeeding: discontinue use and advise cessation of nursing.
  • Thyroid function monitoring: perform baseline and periodic serum TSH/T4 tests.
  • Radiation safety: limit exposure to staff and family members, follow shielding protocols.
  • Renal impairment: assess renal function before administration.
  • Store below 25°C: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Sodium Iodide (Na131I) can interact with several medications that affect thyroid function or iodine handling.

Major Interactions (Avoid)

  • Antithyroid drugs (e.g., propylthiouracil, methimazole)
  • Lithium therapy
  • Amiodarone
  • Concurrent radioactive iodine procedures

Moderate Interactions (Monitor Closely)

  • Beta‑blockers (may mask hyperthyroid symptoms)
  • ACE inhibitors (potential impact on renal iodine clearance)
  • Calcium or iron supplements (may reduce oral absorption)

Frequently Asked Questions

Jodek Sodu Na131i Polatom contains sodium iodide labeled with the radioisotope I‑131. It is used for thyroid imaging, to treat hyperthyroidism, and as a therapeutic agent for thyroid cancer, providing both diagnostic visualization and targeted radiation.

After oral administration, sodium iodide is actively transported into thyroid cells via the sodium‑iodide symporter. The I‑131 isotope emits beta particles that destroy thyroid tissue and gamma photons that can be detected with a scanner, enabling imaging and therapeutic ablation.

The prescribed dose is determined by the treating physician based on the specific indication, patient weight, thyroid function, and radiation safety considerations. Dosing regimens are individualized and should follow local regulatory guidelines.

Use during pregnancy is generally avoided because the radioactive iodine can affect the fetal thyroid. Breastfeeding mothers should discontinue the medication and stop nursing until the radioactivity has cleared, as recommended by a qualified healthcare professional.

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 and any necessary import documentation.

Compared with non‑radioactive antithyroid drugs, sodium iodide (Na131I) offers a single‑dose or short‑course option that directly ablates thyroid tissue, often reducing the need for long‑term medication. It differs from other radioactive iodine products mainly in isotopic purity and regulatory status.

Store the product below 25 °C in its original packaging, protecting it from moisture and direct sunlight. Ensure the container remains sealed until use and handle with standard radiation safety precautions as outlined in the product labeling.

The medication is taken orally, usually as a single dose or a short series of doses, depending on the clinical indication. Patients should follow the prescribing physician’s instructions regarding fasting status and timing relative to other medications.

Serious risks include severe hypothyroidism requiring lifelong hormone replacement, bone‑marrow suppression leading to low blood counts, and rare allergic reactions such as anaphylaxis. Patients should be monitored closely for these events, especially after high‑dose therapy.

Contraindications include patients with known hypersensitivity to iodine or radioactive iodine, pregnant women unless absolutely necessary, and individuals with uncontrolled thyroid storm. Patients with severe renal impairment should also be evaluated carefully before use.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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