Dysautonomia (Autonomic Dysfunction) Community
midodrine effects
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This patient support community is for discussions relating to Dysautonomia (Autonomic Dysfunction) including: Postural orthostatic tachycardia syndrome (POTS), neurocardiogenic syncope, mitral valve prolapse dysautonomia, pure autonomic failure, autonomic instability and others.

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midodrine effects

i have just started on midodrine to help with my POTs condition I have been on it 3 weeks now but since starting it I feel continuously tired, I have lost my appetite, I have a continuous headache and feel quite down and can not get up and going which is not normally like me at all, I have also had some of the other side effects as well but not so worried about them, just want to know is this normal, if so how long does it last as I am really thinking about stopping it as although the alternate of passing out is not much better at least I felt semi ok before taking it , please help regards Pauline x
612876_tn?1355518095
Three weeks is a pretty good length of time to test midodrine. It sounds like this may not be the right medication for you. Not to worry, there are many different medications that can be used to treat POTS, you just have to hang in there through some trial and error to find the right one or the right combination. I recommend calling the doctor who rxed you the midodrine, and explaining what you've just said here. Ask if s/he recommends a dosage adjustment, discontinuing the midodrine and starting something else, or taking something in addition to the midodrine.

You are not alone. A significant proportion of POTS patients don't tolerate midodrine for one reason or another, so don't feel discouraged! Hang in there and know that our community is here to support you, H.
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