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On Fludrocortisone for POTS, every few months I have to increase the dose as it stops working I'm now on 0.4mg. why does it stop working and I have to keep increasing the dose?
Is Florinef (fludrocortisone) 0.05 mg daily bad to be on longterm for POTS syndrome? Is it better than low dose prednisone? Can't keep seem to control w/ just h20&salt
Is Florinef (fludrocortisone) 0.05 mg daily bad to be on longterm for POTS syndrome? how long is too long?risk of osteoporosis? Is it better than low dose prednisone?
Diagnosed w/POTS syndrome. Feel much better on florinef (fludrocortisone) & beta bloceker. Explain why doc wants me to stop all meds & get catecholamine test.Necessary?
Is Florinef (fludrocortisone) 0.5 mg every other day bad for my bones?(I POTs syndrome & can't function without it.) Is it as bad as a steroid as low dose prednisone?
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