Experiences with

CellCept

I want to know if anyone has had this and if getting off cellcept and/or tacrolimus reversed it?

I was placed on Cellcept for autoimmune attacking my liver. Now I have low platelets and low white blood cells. Seeing the hepatologist in 2 weeks, but I called nurse and she said it was the liver cirrhosis and not new meds. So my regular doc wants me to see a hepatologist today.

I was placed on Cellcept for autoimmune attacking my liver. Now I have low platelets and low white blood cells. Seeing the hepatologist in 2 weeks, but I called nurse and she said it was the liver cirrhosis and not new meds. So my regular doc wants me to see a hepatologist today.

She also said I should stop Cellcept temporarily. Now I feel a bit better, temp is 36C, but my throat still aches and body feels weak. Only partial tests ready up now, eosinophils are at 0. My two main concerns - do I need some antivirals? And I'm really terrified of stopping Cellcept.

Does MCOPHENOLATE/CELLCEPT stop these areas from growing ?

has anyone declined cytoxan and had success with cellcept in treating kidney injury? My son has had Eculizumab and Rituximab with no success and is now declining rapidly with kidney function.

Cellcept had run its course on day 35. It is an effective medication with controlling GVHD (GraftVsHost Disease). I also had a switch from Tacrolimus to Sirolimus. Both of these meds help with the GVHD.

They are refusing to prescribe me CellCept (been on it for 4 years)! But are supplying me Myfenax instead which is a generic. I thought that Mycophenolate brands were not interchangeable and you are advised to remain on the same brand? Is this correct?

I'm on 500mg Cellcept 2x/day and 1mg Tacrolimus 2x/day. The tacro is the issue with skin cancers. They are suggesting Prednisone which I am very hesitant to switch to.

After years of receiving my prescription of Roche MMF from my Doctor’s surgery, recently I have been switched to the hospital pharmacy & have been taking a version made in India by Ascend. I am hoping this has also happened to a few here & they could reassure me that they too have noticed the change

I had never had any psoriasis that I knew of until around 3 months after I was switched from Tacrolimus/Envarsus and Cellcept to Belatacept infusions. I had a few spots on my arms that developed.

I'm on low dose prednisone, hydroxychloroquine, arcoxia, cellcept etc and I also have a wound called pyoderma gangrenosum. Over the last 6 months or so. My menopause symptoms have become so bad that I'm seriously considering hrt.

I’ve been taking Cellcept for 3 months now with no serious side effects and think I’m seeing benefits now. Hardly any pain which is something I never imagined saying!!

I am on 5mg of Presidone, 1mg Tacrolimus am, .5 Tacrolimus pm and Cellcept daily and am experiencing pain in different parts of my body, ex. hand, fingers, feet, toes, arms, on a regular basis.

Has anyone had oral thrush associated with taking Cellcept? I have been on Cellcept for three months and IVIG for 14 months. Today, the inside of my lower lip exploded with white bumps. My research indicates that Candida is common side effect of immune suppression.

I currently do cellcept 500mg twice a day and beletacept infusion once a month. Please share with me your meds and how much. I am trying to gain full perspective on long term living. Thank you all so much. Much love ❤️

was only a 60% when they harvested it.So switched me from tacro to beltacept but during the transition had me still on tacro for a month too,which in turn lowered my i.mune system so much that body one big bruise of red spots and bruises and also i picked because of being on the beltaceot,tacrolimus,cellcept

I’m on week 2 of cellcept up to 1000mg a day and so far side affects are not too bad, but too soon to notice improvements. my question is, should I contact rheumatologist and ask to stay on prednisolone for longer?

has anyone had many difficulties with nausea while on cellcept? I seem to be struggling a bit and think cellcept may be the culprit. Thanks

doctor who ordered the followup cMRI wrote me in the patient portal and said that he wanted to see another cMRI in three months, and at that time if it is not completely cleared, he wants to give me one of two drugs: Azathioprine (known in the US also as Imuran) or mycophenolate (also known in the US as CellCept