Product image of Jodek Sodu Na 131i Narodowe Centrum Badań Jądrowych (Sodium Iodide (131i)) supplied by GNH India

Jodek Sodu Na 131i Narodowe Centrum Badań Jądrowych

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

Jodek Sodu Na 131i Narodowe Centrum Badań Jądrowych (Sodium Iodide (131i))

Sodium Iodide (I-131), the active ingredient in Jodek Sodu Na 131i Narodowe Centrum Badań Jądrowych, is a radiopharmaceutical presented as a solution for injection for intravenous use. It is employed to visualize thyroid tissue, detect metastatic thyroid cancer and assess overall thyroid function in patients requiring diagnostic imaging.

GNH India supplies Jodek Sodu Na 131i Narodowe Centrum Badań Jądrowich as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals worldwide.

Manufacturer / TM Owner

Narodowe Centrum Badań Jądrowych

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Indications & Clinical Uses

  • Jodek Sodu Na 131i Narodowe Centrum Badań Jądrowych is used in diagnostic procedures that target the thyroid gland and related pathologies.
  • Thyroid scintigraphy: provides functional imaging of thyroid tissue distribution for diagnostic evaluation.
  • Thyroid cancer metastasis detection: identifies iodine‑avid metastatic lesions to guide staging.
  • Thyroid function assessment: evaluates gland activity and hormone synthesis capacity in clinical investigations.

How It Works

  • Sodium Iodide (I-131) is selectively taken up by thyroid follicular cells via the sodium‑iodide symporter. Once inside the gland, the radioactive iodine emits beta particles that cause localized radiation and gamma photons that are captured by imaging equipment, allowing visualization of thyroid tissue and functional assessment without significantly affecting surrounding structures.

Side Effects

Adverse reactions may occur following intravenous administration of I‑131 diagnostic solutions.

Common Side Effects

  • Nausea or mild vomiting
  • Transient headache or dizziness
  • Temporary alteration of taste sensation
  • Mild injection‑site pain or erythema
  • Low‑grade fever or chills

Serious or Rare Side Effects

  • Allergic reaction including urticaria or anaphylaxis
  • Radiation thyroiditis causing painful swelling
  • Hematologic changes such as leukopenia
  • Pulmonary radiation pneumonitis (very rare)
  • Severe radiation‑induced organ injury in high‑dose exposures

Precautions & Warnings

  • Prior to use, clinicians should evaluate patient‑specific factors and follow radiation safety guidelines.
  • Pregnancy: avoid unless essential, as fetal thyroid may be exposed.
  • Breastfeeding: discontinue nursing or consider alternative imaging.
  • Baseline thyroid function: assess before administration to interpret results accurately.
  • Radiation safety: implement shielding and limit exposure for staff and nearby patients.
  • Concurrent iodine‑containing drugs: review and possibly withhold to prevent uptake interference.
  • Store at 2-8°C: keep refrigerated, protect from light, do not freeze or shake.

Avoid Interactions

I‑131 diagnostic agents can interact with substances that alter iodine handling or thyroid activity.

Major Interactions (Avoid)

  • Therapeutic doses of stable iodine (e.g., potassium iodide) – blocks thyroid uptake.
  • High‑dose thyroid hormone suppressive therapy – may reduce diagnostic accuracy.

Moderate Interactions (Monitor Closely)

  • Amiodarone – high iodine content, may affect uptake.
  • Iodinated contrast agents – schedule imaging to avoid interference.
  • Antithyroid medications – may diminish tracer accumulation.

Frequently Asked Questions

Jodek Sodu Na 131i Narodowe Centrum Badań Jądrowych is a diagnostic radiopharmaceutical used to image the thyroid gland, detect metastatic thyroid cancer lesions, and assess overall thyroid function through scintigraphic techniques.

Sodium Iodide (I-131) is actively transported into thyroid cells by the sodium‑iodide symporter. The radioactive iodine emits gamma photons that are captured by a gamma camera, producing images that reflect the functional activity and distribution of thyroid tissue.

The administered activity of I‑131 for diagnostic purposes is determined by the prescribing physician based on the specific clinical indication, patient size, and imaging protocol. Exact dosing is individualized and not standardized in public literature.

Use during pregnancy is generally avoided because the fetal thyroid can absorb radioactive iodine, potentially causing harm. Breastfeeding mothers should discontinue nursing or consider alternative imaging, as I‑131 can be secreted in breast milk.

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

Sodium Iodide (I-131) offers both therapeutic beta emission and diagnostic gamma emission, allowing simultaneous imaging and potential treatment. Alternative agents such as I‑123 provide pure gamma emission with lower radiation dose, but lack therapeutic capability. Choice depends on clinical goals, radiation safety considerations and regulatory approvals.

The solution for injection should be stored at 2‑8 °C, protected from light, and kept in its original container. Do not freeze or agitate the vial, and use aseptic technique when preparing for intravenous administration.

Jodek Sodu Na 131i is administered intravenously by a qualified healthcare professional. The radiopharmaceutical is injected as a sterile solution, after which imaging is performed according to the prescribed scintigraphy protocol.

Serious risks include allergic reactions ranging from urticaria to anaphylaxis, radiation‑induced thyroiditis, and rare hematologic or pulmonary complications from radiation exposure. Prompt recognition and management of these events are essential.

Patients with known hypersensitivity to iodine or radiopharmaceuticals, pregnant women unless absolutely necessary, and individuals who have recently received large therapeutic doses of iodine should avoid this agent. Clinical judgment should guide exclusion.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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