Cellcept patient information

Common Questions and Answers about Cellcept patient information

cellcept

Avatar n tn I know cellcept is a class D drug, and discussed my concern with my doctor. She said that patient on cellcept have had successful pregnancies, even though she legally would have to tell me that it is not recomended because of the class D warning, but she didn't seem overly concerned about the fact that I want to get pregnant someday. I'm 26 years on and married, and not ready to give up hope of having my own child.
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.
984010 tn?1255796138 Thanks for the website I checked it out and there is alot of information. I have been given several differant meds but afraid to take any. Oxycodene, Gabapentin, Amitriptyline, Hydroxycholroroquine. I do take a multi-vitamin for anemia. Yes the ANA came back positive Pattern: Nucleolar Titers >1:640 SED 13, SS-A 0.4 and SS-B >8.0H AI. Lip biopsy came back positive for Sjogrens.
Avatar f tn 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???
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).
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.
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.
645800 tn?1466860955 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.
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 My husband had autoimmune hepatitis and had liver transplant in March of 2003, he is doing well however, he stopped taking his meds 3 months ago because the meds is very expensive as he say, now he went back to take his meds that is Cellcept and Prograf . He now is feeling pain on his left side of his belly and it is really like distended and hard.and very warm to touch. His belly like shifted to the left ever since he had the surgery.
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.
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 Is Cellcept the only immunosuppressive he's currently taking? My understanding is that Cellcept is usually combined with another drug - a calcineurin inhibitor for example. It seems unlikely and perhaps dangerous to stop all anti-rejection drugs and initiate treatment for HCV. It sounds like fertile ground for acute organ rejection so I assume he is going to take some kind of immunosuppressive drug. Any information would be welcome Hector.
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?
686869 tn?1227199935 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.
Avatar f tn 5mcg and 800 mg ribavarin for 18 months. Usually they say 12 months but since he is a transplant patient they will keep him 18 months on a lower dose. After the 18 months he is considered a nonresponder. He was off the shots for 1 month and his bloodwork went crazy. ALT400s, AST300s, GGT568 and viral load 4 million. They did a biopsy and it showed rejection and also hepc attacking new liver. So he is starting alll over again with cellcept, more prednisone, more prograf.