For those of you who take Cellcept, have you noticed anything different in your MG symptoms since switching from Brand name CellCept to Generic?

I have been on Cellcept for 4 years and my MG was under control. I began feeling MG symptoms again around late May and that was when I switched from Name Brand Cellcept to Generic. I am seeing a MG specialist on Wednesday and just wondering if anyone else has noticed anything different when they switched.

I am probably reaching but I am very in tune with my body and can usually pinpoint when something has an effect on my MG. It's just strange to me that after years of being on a treatment therapy of Mestinon, Cellcept and IVIG that my condition has changed like it has. This one has had me stumped for a few months now.


Thanks