Derek1987 Posted September 6, 2020 Report Share Posted September 6, 2020 My coreg was upped to 25mg twice a day and my autonomic dr. added Fludrocortisone 0.1mg once a day in the morning to take with my coreg. This was a decided route because i have low renin and low aldosterone which was was discovered by my endocrinologist. I just had the appointment and already forgot how this is supposed to help me with the hyperadrenergic problem. I was also just diagnosed with Heds. Not sure if this relates. Can someone shed some knowledge on every single way this medicine can help me? Thanks for the knowledge. My pharmacist said i cant take the Fludrocortisone and ibuprofen together. Why is that?(my wife picked it up and told me this) Quote Link to comment Share on other sites More sharing options...
Guest KiminOrlando Posted September 6, 2020 Report Share Posted September 6, 2020 I take Fludrocortisone and ibuprofen. Maybe it was specifically for you? Or has nobody told me the last 12 years? Quote Link to comment Share on other sites More sharing options...
dancer65 Posted September 6, 2020 Report Share Posted September 6, 2020 If I remember correctly taking them together can cause gastric inflammation . Quote Link to comment Share on other sites More sharing options...
p8d Posted September 6, 2020 Report Share Posted September 6, 2020 The fludricortisone helps your body retain fluids to keep BP up and reduce OH. Keep an eye on your BP while starting it. Mine got very high on a quarter tablet. I, too, have hyper POTS. Quote Link to comment Share on other sites More sharing options...
Sushi Posted September 6, 2020 Report Share Posted September 6, 2020 19 hours ago, Derek1987 said: was also just diagnosed with Heds. Not sure if this relates. Do you mean hypermobile EDS? If so, many of us have it along with Dysautonomia though I don’t think there is definitive research on why. I too have hypermobile EDS. Quote Link to comment Share on other sites More sharing options...
Pistol Posted September 6, 2020 Report Share Posted September 6, 2020 38 minutes ago, Sushi said: If so, many of us have it along with Dysautonomia though I don’t think there is definitive research on why. I too have hypermobile EDS. @Sushi - as far as I know EDS causes the walls of the blood vessels to be too elastic ( like your joints and cartilage, from too much collagen ) and therefore the vessels are not able to constrict properly. This in turn can trigger the ANS to try to compensate by telling the vessels to constrict by activating the sympathetic NS ( adrenaline ). Quote Link to comment Share on other sites More sharing options...
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