Sodium Iodide is classified into drug class of minerals and electrolytes and is sold under the trade names of “Iodopen” and “Scleroderma”. It is a supplement that is used to replenish electrolyte levels in the body when they're depleted by other means. It is also commonly used in veterinary medicine as an iodine supplement. It is mainly used to treat hyperthyroidism. Radiolabeled Iodide I-131 is used to evaluate thyroid function, morphology, and functions as a diagnostic tool. It is also indicated to treat iodine deficiency in the body. Speak to your doctor if you experience any of the following signs or symptoms that may indicate a very serious side effect: a rash, hives, itching, blistered or peeling skin with or without fever, wheezing, tightness in the chest or throat, difficulty breathing, swelling of the lips, tongue or throat are all symptoms of an allergic reaction, unexplained bleeding or bruising, fever, pain in the joints, and swollen gland. It is contraindicated in patients with; hyperthyroidism TB involving the lungs, decreased kidney function, pregnancy, iodine hypersensitivity, and urticarial vasculitis. Studies have shown that Sodium Iodide is harmful to an unborn baby. It is not recommended for pregnant women. Breast milk excretes iodine. Breastfeeding mothers who need the treatment of this pharmaceutical medicine, are strongly advised to give their infants formula milk. This pharmaceutical medicine was approved in August 1971, by the U.S Food and Drug Administration.

Thyroid hormones are produced by the thyroid gland, which stores Sodium Iodide I 131 in the thyroid gland. Because of this, the thyroid gland is damaged by the trapped Sodium Iodide 131. So, thyroid gland activity is reduced as a result.

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