Corlanor vs Ivabradine. Please help!
Hi all! 29F here and I’ve been on Corlanor since 2019, when I was first diagnosed with POTS. I have been thrilled with it all these years and find it very helpful. I am very fortunate that my prescription insurance covers it 100%. I went to refill it and it was out of stock at every single pharmacy nearby except one. I refilled it and instead of showing Corlanor, it showed the generic, Ivabradine. I spoke with the pharmacist and she told me they will order Corlanor for me. I got an alert that it’s ready for pickup but it says Ivabradine and not Corlanor. I know Amgen discontinued it or something, so I’m wondering if it’s just not available anymore. I’ve heard horror stories about the generic not working as well. I’m wondering if anyone has any positive stories? I will not be able to function if my medication doesn’t work properly and I work an active job, and it’s very hot in Southern California right now. Unfortunately, I can’t afford it from a Canadian pharmacy especially because I take two different dosages for AM and PM. I’m having the worst anxiety over this.