cellcept warnings

about those warnings - absolutely everything these days come with lengthy, scarey warnings. If we assumed all the worst would happen to us, we would never take another pill again. You have to weight the benefits versus the risks and make your decisions with all the information you can gather.

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.

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!!!!

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.

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.

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?

everything was great for first 7 mths. Then they changed his transplant meds from prograf and cellcept to rapamune and cell cept. Thats when it all went bad. He went into resp. arrest 4 times in 1 month, kidney failure, acted like he was drugged, twitched, and spent many weeks in the hosp. We tried to tell the docs that it was the new meds, he was also on vancomycin, and they would not listen they kept saying it was the pain meds he had been taking for years but we knew better.

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?

I take Cellcept for 2 and a half year. How long will last taking of this medicine because my hair and stomack can't stand it any more?

i think the Dr wants to start, cellcept and eliminate diazapam nd steroids....after having such relief finally,after so long.. I am afraid.Also of the side effects of cellcept and having massive pain returned. But which side effects are going to be worse? Preds or cellcept. I will research and let you know,. There are other drugs, but with heart and clogged arteries, i am not a candidate... Hang in there. Advil helps. Tons of it, Percocet if you can find a Dr who will write it,.....

When that happens, the doctor increases PanGraf / Cellcept dosage and a particular steroid (wysolone). After that the enzymes go back to normal - except GGT which goes down but still remains well above normal (say, falls from 1800 to 300).

5mg and tenofovir 300mg) and prograf, cellcept wysolone etc. Two months back entacavir was withdrawn and I am now treated with tenofovir, prograf(6mg), cellcept(1000mg) and Magnesium suppliment. Almost at the same time( 2months back) I suffered from maleria also. Since then SGOT and SGPT are gradually rising from normal level, and they are now 69 and 46 level( normal range is 4) and rose to 3.2 almost one month back but it goes down to 2.3 now. What could be reason?

s, and indicators do heart issues, my question is does cellcept work as well? does morbidity go up the second time around? Is there something better to use? More chest pain this time. thanks for your input!

One more thing I have to worry about is infections due to being on CellCept of my MS. So it tends to freak me out a little bit when I get the chills as that could indicate I am running a fever. Me thinks that maybe I am having a flare? Thanks for listening.

Should the transplant team/doctor monitor liver transplant patients taking cellcept post liver transplant over time? Is there a significant threat of cellcept causing lymphoma?

So I read these articles and it seems that Merk was sued in 2010. I have not read everything on this, but wouldn't you think major warnings would have come out about this 3 years ago. I wonder if removing the chip is an option Such a shame. This was the "Holy Grail" for identification. Seems the more we take care of our kits (chips, vaccinations, meds) the more harm can be done.

s Hospital yesterday and was told by the doctor that I have Primary Progressive MS. She gave me 3 prescriptions - one for Cellcept to slow the progress, one for PT and the third for a scooter. That last one got me teary. I thought I was years away from that but now see that it is for the best. It will give me what I need to go out more. Also had to get the H1N1 vaccine and the pneumonia vaccine because she said Cellcept suppresses the immune system. Not sure there's much more to say.

Hi Dennis, Welcome back. Has spring sprung in TN yet? The deer here are very active and creating excitement in the area. I had to reread your message - it appears you are saying that the VA doctors are listening to you ? Huh? This is very good news. The 1.5T closed MRI should give them a pretty good look at what is going on if it was done to the MS protocol. Ufrustrated2 had his breakthrough with the VA recently, too.

If so, then the treatment is optimizing doses and levels of cellcept and prograf and trying to minimize the use of parenteral corticosteroids.

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).

s how much she had to take and also Cellcept for her immune system. After 6 months she was totally weened off of Prednisone and will continue Cellcept until her one year mark and get another Renal Biopsy done in April.....I would love to know about more parents that have had children that gave suffered with this horrible virus that has left my daughter scarred physically and emotionally for life. I do not wish this on any innocent child!

Cellcept warnings

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