Has anybody had any experience with Kevzara? It’s relatively new drug that works by inhibiting interleukin 6, very similar to tocizilumab I’m told (which I was on previously).
I’m a little confused as to why they have started me on this drug if it works the same as tocizilumab as I had to come off that due to neutropenia & frequent hospitalisation. Anyway it’s a fortnightly injection which you give yourself. I’ve just had my 3rd dose this morning & been for my first set of bloods so fingers crossed they come back ok because this is the last drug for me.
Would love to hear from anyone who’s tried or is taking this.