Cellcept indications

Common Questions and Answers about Cellcept indications

cellcept

Avatar n tn 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.
Avatar n tn 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!!!!
Avatar f tn 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.
Avatar f tn 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.
778275 tn?1326913623 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.
Avatar f tn 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?
1135761 tn?1260557094 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?
Avatar f tn 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.
Avatar n tn when you say adding some cellcept might be a good idea,does that include trying to lower my prograf some?
Avatar f tn 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?
Avatar n tn 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,.....
Avatar f tn 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).
Avatar m tn 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?
Avatar f tn Hi, I too have been DX with the same as you and also have tried many SSRI's and have not been able to tolerate. I didn't know that people with Fibro have a sensativity to meds. No wonder I have been gone through so many meds, my doctors never told me this. I ask my Rhuemy if I could try Sevella, he said NO because it messes with your blood pressure and he refused to put me on it even with the knowlegde that we have tried everything else. I am on Cellcept 2000 mg a day for SLE.
960462 tn?1284991345 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!
Avatar m tn 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?
Avatar f tn 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.
645800 tn?1466860955 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.
Avatar m tn If so, then the treatment is optimizing doses and levels of cellcept and prograf and trying to minimize the use of parenteral corticosteroids.
Avatar f tn 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).