Ivabradine tips?
After literally 20 years of doctors dismissing me as a hysterical woman in a variety of ways, I just got my official POTS diagnosis yesterday. (Yay? Condolences to me? All of the above?)
I'm going to start on 5mg ivabradine twice daily, as soon as the prior authorization goes through with my insurance. I'm a bit nervous -- I know a lot of you can relate to the fear of making things worse -- but mostly crossing my fingers so hard. If it can help even 10% with this awful fatigue and inability to exert myself, it'll change my life entirely.
I'm concerned though because my heart rate often drops quite low (50s) when I'm sleeping. In theory I'm meant to be taking this 12ish hours apart, right? My heart rate typically only does the tachycardic thing when I'm upright, around the 140-160bpm range.
Does anyone else have this issue and take ivabradine? Is that something to worry about? (I didn't quite get the chance to ask my cardiologist. I often forget to ask in the pressure of the moment and then they're so busy/hard to get hold of.)
Other than that, any tips or things to watch out for when starting this med? Thanks in advance! ❤️