sodium iodide I 131, Iodotope, Sodium Iodide I 131 Therapeutic (cont.)

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STORAGE: Sodium iodide I 131 should be store at room temperature, 20-25 C (68-77 C). Sodium iodide I 131 is ordered for individual patients in a hospital setting. It arrives at room temperature in a lead container to minimize radiation exposure to hospital personnel. Special handling is required.

PRESCRIBED FOR: Sodium iodide I 131 is used to treat hyperthyroidism and some cases of thyroid cancer.

DOSING: The usual sodium iodide I 131 dose ranges from 4-10 mCi to treat hyperthyroidism. Doses to treat thyroid cancer are individualized and are usually 10-27 times greater than for hyperthyroidism.

DRUG INTERACTIONS: Non-radioactive iodine, thyroid hormone, propylthiouracil (PTU) or methimazole (Tapazole, Northyx) may all interfere with the trapping of sodium iodide I 131 by the thyroid gland. Thyroid hormone, drugs that contain iodine (for example, amiodarone [Coradone]), and iodine containing contrast agents all interfere with the action of sodium iodide I 131.

PREGNANCY: Sodium iodide I 131 has been shown to cause harm to a developing fetus. Use in pregnant women should be avoided.

NURSING MOTHERS: Iodine is excreted in breast milk. Therefore, formula feedings for infants are strongly recommended for nursing women requiring sodium iodide I 131 treatment.

SIDE EFFECTS: The side effects commonly seen with sodium iodide I 131 treatment are mild with the smaller doses given for hyperthyroidism but may be more severe with the larger doses given for thyroid cancer. Sodium iodide I 131 may cause suppression of the bone marrow, resulting in anemia, and reductions in white blood cells and platelets. It also may cause acute leukemia.

With large doses, radiation sickness manifest by symptoms of nausea, vomiting, chest pain, increased heart rate, itchy skin, rash, hives, and possibly death, also may occur.

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