I am 11 years post-kidney transplant. I have been on the same drug regime for the last 11 years as well, 5mg predisone, 360mg of Myfortic, and 2mg tacrolimus in the morning, 1mg at night. About a year ago I switched to a different transplant hospital from the one I was transplanted in due to moving cities. This new transplant clinic has a great reputation and does many transplants as well. I had my second clinic appointment with the new clinic yesterday and say the transplant program medical director. She told me about some new drugs that have come out on the market since my transplant 11 years ago and wants me to switch, although she left it open for me to research and decide. Obviously, I am pretty nervous since I've been on the same medications for 11 years without any rejection episodes.
The first drug is the Envarsus/Astagraf, which is basically an extended release tacrolimus that you take once a day instead of twice a day. Supposedly you have a more consistent tacrolimus level and it is less toxic long-term on the transplanted kidney. That all sounds pretty great to me. Has anyone made the switch from regular tacolimus to the extended release and did everything go okay?
The second drug we discussed is Everolimus/Zortress, which I had never ever heard of before. It would take the place of the Myfortic and her exact words were "if I was a transplant patient, that's what I'd want to be on". Basically, the Myfortic is tearing up and damaging my digestive track. I've been dealing with chronic diarrhea from the Myfortic for many years. Supposedly, this medication does not have that side effect. Does anyone have any experience with this medication?
It seems like there are so many more drugs for transplant patients on the market now that when I was first transplanted. I'm sure that progress and improvements in anti-rejection medications are a good thing, but it is a bit overwhelming and scary to change. Any experience anyone has had is appreciated.