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

Moniyot-131

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

Moniyot-131 (Sodium Iodide (131i))

Sodium Iodide (I-131), the active ingredient in Moniyot-131, is a Radiopharmaceutical presented as an oral radiopharmaceutical for oral use. It is used to treat hyperthyroidism, to ablate residual thyroid tissue after thyroid cancer surgery, and to enable diagnostic imaging of thyroid function in patients with thyroid disorders.

GNH India supplies Moniyot-131 as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide. The company adheres to EU manufacturing standards and provides global distribution with regulatory support, ensuring product integrity and timely delivery.

Manufacturer / TM Owner

Monrol Europe Srl

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Indications & Clinical Uses

Moniyot-131 acts on thyroid tissue and is employed in the following clinical situations:

  • Hyperthyroidism: reduces excess thyroid hormone production by destroying overactive thyroid cells.
  • Thyroid cancer (ablation): eliminates residual thyroid tissue after thyroidectomy to reduce recurrence risk.
  • Diagnostic imaging of thyroid function: provides gamma emission for scintigraphic visualization of thyroid uptake.

How It Works

  • Sodium Iodide (I-131) is a radioactive isotope that mimics stable iodine and is actively taken up by the sodium‑iodide symporter in thyroid follicular cells. Once inside the gland, beta particles emitted by I-131 cause localized cellular damage, leading to tissue ablation, while concurrent gamma photons permit external imaging of thyroid distribution. The selective uptake allows targeted therapy with minimal systemic exposure.

Side Effects

Oral administration of I-131 may be associated with the following adverse reactions.

Common Side Effects

  • Nausea or vomiting
  • Dry mouth or altered taste
  • Transient hypothyroidism
  • Neck discomfort or pain
  • Mild fatigue

Serious or Rare Side Effects

  • Severe hypothyroidism requiring hormone replacement
  • Bone marrow suppression leading to cytopenias
  • Radiation thyroiditis with painful swelling
  • Allergic reactions including rash or anaphylaxis
  • Pulmonary fibrosis (rare)

Precautions & Warnings

Prior to prescribing Moniyot-131, clinicians should observe these safety considerations:

  • Pregnancy: contraindicated (Category X); avoid use in pregnant patients.
  • Breastfeeding: not recommended; discontinue breastfeeding during and after treatment.
  • Thyroid function monitoring: assess serum TSH and thyroid hormone levels before and after therapy.
  • Radiation safety: advise patients on limiting close contact with others, especially children and pregnant women, for a specified period.
  • Dosage individualization: determine activity based on patient’s thyroid uptake and clinical status under specialist supervision.
  • Store below 25°C: keep in original container, protect from moisture and light.

Avoid Interactions

I-131 can interact with several agents that affect iodine handling or radiation response.

Major Interactions (Avoid)

  • Antithyroid drugs (e.g., methimazole, propylthiouracil): reduce iodine uptake and diminish therapeutic effect.
  • Lithium: interferes with thyroid hormone release and may increase radioiodine retention.
  • Potassium iodide or stable iodine supplements: block I-131 uptake, rendering treatment ineffective.
  • Radioprotective agents (e.g., amifostine): may protect thyroid tissue from intended radiation damage.

Moderate Interactions (Monitor Closely)

  • Beta‑blockers: may mask symptoms of thyroid hormone changes after therapy.
  • Calcium or iron supplements: can modestly affect gastrointestinal absorption of oral I-131.
  • ACE inhibitors: monitor renal function as altered clearance may influence systemic exposure.

Frequently Asked Questions

Moniyot-131 is a radiopharmaceutical containing Sodium Iodide (I-131) that is used to treat hyperthyroidism, to ablate residual thyroid tissue after thyroid cancer surgery, and to provide diagnostic imaging of thyroid function through scintigraphy.

I-131 mimics natural iodine and is taken up by thyroid cells via the sodium‑iodide symporter. Inside the gland, emitted beta particles cause localized cellular destruction, while gamma emissions allow external imaging of iodine distribution.

The administered activity of Moniyot-131 is individualized by the prescribing specialist based on the patient’s thyroid uptake, disease severity, body weight and clinical objectives. No fixed dosing regimen is provided in public literature.

Moniyot-131 is classified as Pregnancy Category X, meaning it is contraindicated in pregnant patients due to the risk of fetal radiation exposure. Breastfeeding is also not recommended; patients should discontinue nursing during and after treatment.

Enquiries are submitted via the product page on gnhindia.com where the required quantity is entered. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details (including any cold‑chain requirements) and import documentation.

Compared with antithyroid drugs or surgery, Moniyot-131 offers a non‑invasive, targeted approach that can both treat hyperthyroidism and ablate thyroid tissue in a single course. It provides the added benefit of diagnostic imaging, but requires careful radiation safety measures and may lead to hypothyroidism requiring lifelong hormone replacement.

Store below 25 °C: keep the product in its original packaging, protect it from moisture and light, and ensure the container remains sealed until use.

Moniyot-131 is administered orally. The patient swallows the prescribed dose with a glass of water, usually on an empty stomach, following specific instructions from the treating physician regarding timing and any dietary restrictions.

Serious risks include severe hypothyroidism requiring hormone replacement, radiation‑induced thyroiditis with painful swelling, bone‑marrow suppression leading to cytopenias, and rare allergic reactions such as anaphylaxis. Monitoring of thyroid function and blood counts is essential after therapy.

Moniyot-131 should not be used in pregnant or breastfeeding individuals, patients with known iodine allergy, those who have received recent large doses of stable iodine, and patients for whom radiation exposure is contraindicated, such as certain pediatric cases without specialist oversight.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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