cellcept dialysis

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.

that affected my legs so my Dr. just prescribed Cellcept. I filled the prescription yesterday and was scared to death after reading the literature on it. What is PPMS? I will be interested in seeing if anyone has used this medication too. Sunnyb.

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?

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?

it had to be increased. Then we went to 500mg of cellcept and 2mg of prograf...it got better. Then we went to 500mg of cellcept and 4mg of prograf and this is where I have been since then. My surgeons told me that I have a very strong immune system and all systems are different. They even told me that most people take less. After the surgeons feel that you are stable they let you go. Now you must find someone to monitor your care and blood work. I get blood work done every 2 months now.

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!

s at his sources of the MRSA, he is now on dialysis, and fighting to live. They chemically sedated him and are unable to wake him up. His condition has been unchanged for 3 weeks. I called and asked what his ammonia levels were last week. The nurse gave me the run around and said they were within normal limits. Without the limits in fornt of me I don't know what they are.

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?

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.

Hi, My dad (78 years old) is on dialysis since last year due to kidney failure, on top of that he has a Coronary Heart Disease since 2000, so he is on meds. He does 3x a week then reduce to 2x week dialysis. Since last July of this year my dad has been experiencing too much weakness than normal. He can barely walk anymore. Then, he started having too low BP after each dialysis to the point that he passes out & sometimes get stiff.

Kidney dialysis can lower the blood pressure causing problems with the heart. If the blood pressure drops too far, the liver shuts down due to the heart not pumping properly. If the kidney dialysis is not started, the failing kidneys will make the heart worse. If the kidney dialysis is started, it could prove fatal. Kidney dialysis can do done in hope that it will not drop the blood pressure down too far. If the kidney dialysis is not done, the heart will suffer.

i want him to live longer,is it possible for him to live longer if he will not undergo dialysis?how long?or if he will undergo dialysis,what will happen if he decided to stop after 5-6 sessions of dialysis?i'm confused,i'm worried about my father's situation but i cannot do anything because i don't know what actions will i take.please help me!thanks.... This discussion is related to <a href='/posts/show/251769'>end stage CHF - life expectancy?</a>.

Cellcept dialysis

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