Has anyone experienced low white blood cell counts from Cellcept? I had an appt with my nephrologist today and that was the one thing he seemed worried about in my blood work. I want to say it was at like 3.1 or something like that (I dont have the results on me). He said he might have to change me back to 1,000 mg 2x a day instead of the 1500 mg 2x a day im on now which kinda scares me since that is the only thing keeping my lupus under control right now.
Anyone with a similar experience?
12/2010- Dx Crohn's Disease
07/2012- Class V Membranous Lupus Nephritis