cellcept mg

Till two weeks back she was on PanGraaf 4mg, Wysolone (steroid) 15mg and CellCept 1000 mg a day. At that time (i.e. two weeks back) her blood result showed that her TLC has slipped to below normal (which is minimum 4) and was showing as 2.8. Her Haemoglobin seems to have settled around 11.2. All other results including Blood, LFT, Creatine etc show normal. Doctor reduced her CellCept to 500 mg (from 1000mg) and increased PanGraaf to 5 mg (from 4mg) and Wysolone (steroid) to 12.5mg (from 15 mg).

I believe the` Herpes antobodies are the cause of my Myasthenia There is a model for that pathogenesis. If you lower my resistence to Herpes with Cellcept, the MG could worsen - doesn't that make sense? Fandangoman, M.S.,Ed.D.

My Dr is trying to lower me off of the prednisone all together and just stay on the cellcept. I was on 10 mg of pred 4 weeks ago, down to 7.5 mg 2 weeks ago and just got reduced to 5 mg. My numbers are staying in great shape, but I am still holding steady on the cellcept. I have been battling AIH for a year and a half. Nothing has worked w/the prednisone accept for cellcept. Since then my numbers have been great. The ast and alt are 19. They were in the 1700's...

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?

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.

PanGraf varies between 2 to three mg (twice) and CellCept between 500 to 750 mg a day (twice, I if I can remember correctly)

I hate to ask my doctors the question of this taking my life and how soon. I am on prednisone that we are weaning off and Cellcept 3000 mg per day. It was considered in the mild to moderate stages, but the docs are not sure how this should be treated. no studies have been done on this and am kinda in limbo....

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!!!!

But my problem is some of my other symptoms are not related to MG. I have problems walking, my giat is wide, I have a Babinski reflex, I have horrible involuntary muscle movements in my legs at night and problems with disfunctional bowel and bladder problems. My doctor ran another blood test and it showed twice a very high fatty acid level or VLCFA. But DNA test did not show ALD. My doctor started me on Zanaflex for the leg muscle problems when she thought I had ALD.

I was diagnosed with Lupus Nephritus IV , my doctor had me do a 3 day IV treatment of 1g solu Medrol , each, that was a week ago. I was already on prednisone 60 mg a day and right before the treatment Cellcept was added. I am feeling like I got hit by bus ! I read elsewhere that most of my current issues are withdrawal from the Solu Medrol . I was wondering if anyone else has had this treatment and how long it took to feel" normal" ?

I am on 750 mg Cellcept 2x a day, 1 mg Prograf 2x a day & 2.5 mg prednisone once a day for my kidney, which has been mine for going-on 33 years. I have been fine but pondering whether I am on too much at this stage. Or maybe this ( and compliance) is the reason that I have been able to keep my kidney for so long??!!

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.

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?

If you could reduce your Prograf dose your kidney function might improve some. I don't know anything about you but at 4 years out your anti-rejection regimen seems rather aggressive. As I understand you you're taking 4 mg Prograf a day and 1000 mg Cellcept. I am 8 years out and I'm taking 2 mg Prograf in the am and 1 mg in the pm.

I had ocular type MG for 10 yrs. and have been on Mestinon 240 mgs daily and cellcept 2000mg daily.I am a healthy 68 yr. old.Just lately I/m noticing cold, sensitive toes and and sciattiaca or nerve pain on complete right side,shoulder,hip to toes on 1 leg only,But both feet have red swollen toes. Drug side effects?

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.

Hi I recently was dx with auto immune encephalopathy...My neuro had me on 2000 mg cellcept daily after we stopped the IV steroids, about 5 month ago I started having deep chest pain shoutness of breath and my collar bone was like getting larger my neuro endo and md said anxiety and put me on meds for depression and stress....I decided to find a different neuro because neuro issues getting worse legs weaker tremors and jerks...the first think she said is cancer can make neruo issues worse.

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?

5mg Prograf bid, Rapamune 3 mg daily, 15 mg prednisone, Cellcept 500 mg qid. The nausea and vomiting has been very hard for him to deal with, and my guess is that increasing the immunosuppression will only worsen those symptoms. The most recent ERCP done last week showed a 6mm discrepancy between the donor and recipient bile ducts with an impression of primary vs secondary sclerosing cholangitis.

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 am prednisone dependent for 20 years (10 mg daily) After dinner I seem to get terribly bloated. No matter what I seem to eat I get this terrible movement that you can see and feel, it is like when you are pregnant and the baby is moving (this is the best way to explain it). Sometimes the pain is worse on the right, but then it moves left (I do have diviticulitis & hiatal hernia(no problem here I stay away from seeds and spicy foods). I do suffer from RA for over 20 years.

The Hep c starting attacking the new liver 4 months after the transplant. The doctors kept him on interferon shots 0.5mcg 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.

The Mestinon will diffently help the mucsles if it is MG. Did he put you on Cellcept also? It sounds like it is MG. This a great group called the Myasthenia Gravis Foundation of America (MGFA) Best of wishes to you.

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?

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