cellcept kidney disease

Stage 5 Chronic Kidney Disease (CKD) can either develop slowly and show few initial symptoms, be the long term result of irreversible acute disease or be part of a disease progression. Acute on chronic renal failure Acute renal failure can be present on top of chronic renal failure. This is called acute-on-chronic renal failure (AoCRF).

I had a breakthrough with Avonex so my dr. recommended adding cellcept to the avonex shots. If so can you tell me how you have done with cellcept. Thanks!!!!

I was just diagnosed with it.

My nephrologist did a biopsy on my kidney and found the lupus in my kidney. Had he not done this we would still be looking. He says that lupus is very hard to diagnose. I have had this for 5 yrs now. I am currently on Cellcept,best drug ever, which there is a generic one now. I was just told thatmy lupus has resolved. I still have lupus, but my kidney function is back to almost normal.

I hope that I have no problems with it and that it does slow the progression of this disease down. Have all the vaccines done. Just waiting for the Cellcept to come in the mail and then I'll start.

My husband had a liver transplant on Aug.5th - and has been **** well. Today he broke out in hives all over his head. He is itching terribly - and the 2nd Benadryl hasn't helped. He is on Cellcept, prograf, and is in a clinical trial (so we don't really know what the extra meds are). Should we be concerned???

I'm a patient with autoimmune hepatitis type II, and my doctor has just perscribed cellcept in an attempt to reduce or stop use of prednizone. It is really important to me to try and have a child, but I'm afraid if I start cellcept that I shouldn't get pregnant. I know cellcept is a class D drug, and discussed my concern with my doctor.

prednisone, IvIG, plasmapheresis, with no real help. My neurologist now suggests therapy with cytoxan or cellcept. He is "saving" the stem cell/bone marrow transplant as a last resort. I have read all of the info on both drugs and the risk/benefit for each. Because this disease robbed me of my life, I am leaning towards cytoxan therapy because it seems to be more aggressive than the cellcept (which is used mainly for transplant rejection).

A friend of mine, a two time kidney transplant patient, takes Cellcept. I don't know why it is being used for MS. I hope someone knows. I am curious.

I had a kidney transplant 4 years ago. About 2 years ago i started having bowels movements that lasts 6-8 hours at a a time and sometimes this will go on for days. I've had a colonoscapy and blood work that would kill a horse and my doctors don't seemed too concerned. this is causing great stress on my body. Please help !!!

The doctor says he proposes to take my mother off CellCept altogether at some point in time and only PanGraaf will be needed for the whole life - in the meantime the doctor may prescribe CellCept in on / off basis.

Went to the Rhematologist for the first time today and I am DX'd with Fibro and SS. I don't understand and know much about these disease and need help. Scared to take meds she gave me.

After a upper respiratory infection last month I have been having someone more weaknesses and even a slight breathing problem at times, so he wants to put me on Cellcept. The problem is Cellcept can cause Lymphoma and other side effects and infection risk,. I want to get off Prednisone due to weight gain and creeping up hypertension and the Mestinin digestive problems are a real pain.

i have had extreme bloating and constant nausea,it seems like it started when they put me on cellcept for autoimmune disease,i also had neison wrap over 3 years ago, i have bowel movements every day,have had your basic tests.all they say is i have a lot of gas in my bowels.

Hi, My mother is diganosed with lupus nephrities ( stage iiia). she is taking cellcept ( 500mg x2) & predisolone ( wysolone 40 mg). what could be the side effects of these drugs. she has a severe stomach pain ( lower abdominal pain) & from last 3-4 days she has back pain as well. nausea & vomiting feeling.

Anyone on cellcept having back pain? I've been having back pain for a couple of weeks now, wake up earlier and earlier in the morning with my back aching and when I move it I get these stabbing pains. It all goes away when I get up, and I've managed to sleep a bit in the morning in a half-seated position, so it's really related to lying down. I just read someplace that cellcept can cause back pain, but I haven't been able to find any info on what kind of pain. Could this be it?

my doctors have reduced my cellcept in half. 1000 mg 2x day to 500 mg 2x day. they said my symptoms are common and reducing the cellcept should help. any comment?

t do well with Lyrica and Methotrexate, I aske my Rheumy about this and he said he would not prescribe it to me because it messes with your blood pressure, so he put me on Cellcept for all my mix connective tissue disease. Cellcept seems to be better than anything I have tried. You should try all the meds your docotrs want because it does take alot of trials to find the correct cocktails.

Patients with kidney failure should be evaluated and treated for chronic kidney disease-mineral and bone disorder, including renal osteodystrophy. Secondary hyperparathyroidism, in particular, should be treated. Treatment is indicated in the immediate posttransplantation period irrespective of bone mineral density because further rapid bone loss will occur in the first several months after transplantation.

While on prednisone you are immunosuppressed which might impede the production of protective or diagnostic hepatitis antibodies. how about medications such cellcept or azathioprine as steroid-sparing agents?

Okay hears the deal I was put on prednison when I was 17yrs old along with imuran, now i know the effects of prednison obviouly, it being a steroid there usually are some weight gain and moon face etc as common side effects. Now I'm 19yrs old and they have me on cellcept. I have always been extremely active even to due to my fatigue but I cannot loose a pound, I will work out 24-7 and change my diets often to see if anything changes and...nothing.

when you say adding some cellcept might be a good idea,does that include trying to lower my prograf some?

He was originally started on a series of Prednisone and Imuron which lasted approximately 7 months, at that point his bone marrow began failing so we had to find an alternative, they felt the Imuron possibly suppressed him too much and he started attacking his bone marrow. In Sept of last year he started Cellcept for which he has now taken for over a year with little problems physically, it does cause some emotional changes as well as affecting his appetite and sleeping.

I was diabetic since I was in 5th grade, but five years ago had a kidney;pancreas transplant. Since then I have been on three kinds of drugs for my transplant. Cellcept, Predizone, and Prograf are the drugs that I am taking. With these drugs along with having diabetes up until 5 years ago affect my chances of producing a child. I am also 32 years of age.

Cellcept kidney disease

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