My consultant is concerned I'm not settling with my medication after 12yrs (A different and better consultant than the previous) and has told me, he's going to increase my Mychophenolate to 6 a day@500mg.
When I first went on these, I was on 5, but I was getting various side effects of headaches, water infections and mild constipation. I'm now on 4 tablets and these symptoms have calmed down/manageable. This consultant says those symptoms were my Lupus, but im not so sure, so a bit weary about going up to 6 tablets this time.
Ive been on Mychophenolate for 8 years now, so any advice/thoughts if anyone is on 6+ tablets? What/not to expect?
Thanks.