Product image of Iodopol (Sodium Iodide (131i)) supplied by GNH India

Iodopol

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

Iodopol (Sodium Iodide (131i))

Sodium Iodide (I-131), the active ingredient in Iodopol, is a radiopharmaceutical presented as an oral solution for oral use. It is employed in the management of thyroid cancer, hyperthyroidism, and as a preparatory ablation before thyroid surgery. The radioactive iodine emits beta particles that selectively destroy thyroid cells while sparing most surrounding tissues.
GNH India supplies Iodopol as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide. The company adheres to EU quality standards and provides regulatory support for cross‑border distribution.

Manufacturer / TM Owner

Narodowe Centrum Badań Jądrowych

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Indications & Clinical Uses

Iodopol is used in thyroid‑related conditions where radioactive iodine uptake is desired.

  • Thyroid cancer (post‑surgical ablation): eliminates residual thyroid tissue to reduce recurrence risk.
  • Hyperthyroidism: decreases hormone production by destroying overactive thyroid cells.
  • Pre‑surgical thyroid tissue ablation: reduces gland size and vascularity before definitive surgery.

How It Works

  • Sodium Iodide (I‑131) is taken up by the sodium‑iodide symporter in thyroid follicular cells. Once inside the gland, the radioactive isotope emits beta particles that cause localized cytotoxicity, leading to cellular apoptosis and necrosis. The short tissue penetration limits damage to adjacent structures, while the gamma emissions allow imaging of iodine distribution. This selective uptake enables targeted ablation of thyroid tissue.

Side Effects

Iodopol may cause a range of adverse reactions, varying from mild to severe.

Common Side Effects

  • Nausea: mild gastrointestinal upset occurring shortly after ingestion.
  • Salivary gland swelling: transient enlargement causing discomfort.
  • Taste alteration: metallic or altered taste perception lasting days.
  • Fatigue: temporary reduction in energy levels.
  • Dry mouth: reduced salivary flow and mild throat irritation.

Serious or Rare Side Effects

  • Severe hypothyroidism: profound reduction in thyroid hormone requiring replacement.
  • Radiation thyroiditis: painful inflammation of the thyroid gland.
  • Bone marrow suppression: decreased blood cell counts leading to infection risk.
  • Secondary malignancy: rare risk of radiation‑induced cancers developing years later.

Precautions & Warnings

When using Iodopol, several precautions should be observed to ensure patient safety and product integrity.

  • Pregnancy: avoid use unless benefits outweigh potential risks, as fetal effects are unknown.
  • Breastfeeding: discontinue breastfeeding or consider alternative therapy due to possible iodine transfer.
  • Renal impairment: assess kidney function and adjust monitoring, as excretion is renal.
  • Thyroid function: evaluate baseline thyroid status and monitor hormone levels after administration.
  • Iodine allergy: contraindicated in patients with known hypersensitivity to iodine compounds.
  • Store below 25°C: keep in the original container, protect from moisture and light.

Avoid Interactions

Iodopol can interact with other medicines; awareness of major and moderate interactions helps prevent adverse outcomes.

Major Interactions (Avoid)

  • Lithium: concurrent use may exacerbate lithium toxicity.
  • Antithyroid drugs (e.g., methimazole, propylthiouracil): reduce efficacy of radioactive iodine.
  • Amiodarone: high iodine content interferes with iodine uptake and thyroid function.
  • Thyroid hormone replacement therapy: may require dose adjustment after ablation.
  • Radioactive contrast agents: can block iodine uptake if administered shortly before or after Iodopol.

Moderate Interactions (Monitor Closely)

  • ACE inhibitors: may alter renal clearance of iodine.
  • Diuretics: affect potassium balance influencing thyroid uptake.
  • Calcium supplements: can reduce oral absorption of iodine if taken simultaneously.
  • Beta‑blockers: monitor heart rate as thyroid hormone changes affect cardiovascular response.
  • Corticosteroids: may modify inflammatory response after iodine therapy.

Frequently Asked Questions

Iodopol is a radiopharmaceutical containing Sodium Iodide (I‑131) that is used to ablate thyroid tissue. It is indicated for post‑surgical ablation of residual thyroid cancer, treatment of hyperthyroidism, and as a pre‑operative measure to reduce thyroid gland size before surgery.

Sodium Iodide (I‑131) is actively taken up by thyroid cells via the sodium‑iodide symporter. Once inside, the radioactive iodine emits beta particles that cause localized cell death, effectively destroying thyroid tissue while sparing most surrounding structures.

The dose of Iodopol is individualized. A qualified prescriber determines the activity (megabecquerels) based on the specific indication, patient’s thyroid uptake, body weight, and clinical goals. No fixed regimen is provided in public literature.

Safety data for Iodopol in pregnancy and lactation are limited. It is generally avoided unless the therapeutic benefit clearly outweighs potential risks to the fetus or infant. Breastfeeding mothers should discontinue nursing or consider alternative therapy because iodine can be transferred in milk.

To order Iodopol, 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 the necessary import documentation.

Iodopol delivers Sodium Iodide (I‑131) in an oral solution, similar to other I‑131 preparations used for thyroid ablation. Differences may lie in formulation, regulatory status, and supplier reliability. Clinically, the therapeutic effect depends on the administered activity rather than the specific brand, provided the product meets pharmacopeial standards.

Iodopol should be stored below 25 °C in its original packaging, protected from moisture and light. The container should remain sealed until use, and any unused portion should be kept away from children and unauthorized personnel.

Iodopol is administered orally as a single‑dose solution. The patient drinks the measured volume under medical supervision, often after a low‑iodine diet to enhance thyroid uptake. No injection or infusion is required.

Serious risks include severe hypothyroidism requiring lifelong hormone replacement, radiation‑induced thyroiditis, bone‑marrow suppression that can lower blood cell counts, and, rarely, secondary malignancies arising from radiation exposure. Patients should be monitored for symptoms such as extreme fatigue, unexplained bruising, or persistent neck pain.

Iodopol is contraindicated in individuals with known iodine allergy, pregnant women unless absolutely necessary, and patients with uncontrolled severe renal impairment where iodine clearance is compromised. It should also be avoided in patients receiving high‑dose antithyroid medications that would negate its therapeutic effect.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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