"The U.S. Food and Drug Administration today granted approval to Lenvima (lenvatinib) to treat patients with progressive, differentiated thyroid cancer (DTC) whose disease progressed despite receiving radioactive iodine therapy (radioactive iodine"...
In the treatment of hyperthyroidism, over-dosage may result in hypothyroidism, the onset of which may be delayed. Appropriate replacement therapy is recommended if hypothyroidism occurs. Radiation absorbed doses to various tissues for any administered dose may be calculated by reference to Table 4 (Absorbed Radiation Doses I-131). (SeebCONTRAINDICATIONS, WARNINGS, PRECAUTIONS sections).
Patients with vomiting and diarrhea should not receive radio-iodide and concurrent antithyroid therapy should be discontinued 3 to 4 days before administration of radioiodide.
Last reviewed on RxList: 10/6/2011
Additional Hicon Information
Report Problems to the Food and Drug Administration
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.
Find out what women really need.