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Diagnosed in late December with hyperthyroid due to hot nodule. Started 3 times a day 5 mgs Methimazole 7 weeks ago, Just had furst labs done last week and saw endoc this morning. He said the Methimazole is moving my t3 and t4 s into range but the bad news is is the drug is effecting my liver. Ugh! He suggested trying the other med ( starts with P). Or RAI, Is it possible if my dose ofMethimazole was reduced to 5 mgs ......the liver wouldn't be effected anymore? He's suggesting 50 mgs of that other anti thyroid med or RAI. Isn't the other med worse as far as side effects? I need help please
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