cellcept and mg

I am considering just staying on Prednizone for a little while longer and getting pregnant, and then going on cellcept. I have been on cellcept one week tomorrow, and think it would not be too late to discontinue (after talking to my doctor again) since I am also still on 40mg of prednizone every day. Do you have any opinions about cellcept and pregnancy?

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?

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).

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.

I am on 5 mg of prednisone and cellcept as well. Can I ask why you stopped taking the cellcept? 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.

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 see ou wrote this a while back but I am hoping you are still here and will see my question. I am supposed to start taking Cellcept for Lupus and I can't find anyone who can tell me anything about how they did on it. Are you there? Did you have any side effects while on it?

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 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 take Cellcept and only Cellcept. I've been on it now for over a month. My MS doctor prescribed it for my PPMS since there's really no treatment for PPMS. I haven't had any side effects from it. When I first started on it, I did get some headaches but nothing I couldn't handle. In my case, I take it to hopefully slow down the progression of my particular form of this disease. Let me know if I can answer any questions.

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.

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?

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?

I have been diagnosed with CIDP, and have gone through the "normal" protocol.. 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.

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. she sched a cat scan and I have a lesion in my right lung.

Hi there:) I just spent three weeks trying very hard to get my body acclimated to Savella because I didn't think that Lyrica was helping. I'd start a titration pack.....get to the 50 mg. oval tablets, and break them in half and sometimes into quarters. I'm convinced that the effect Savella has on norepinephrine was why I couldn't take it.I would get so incredibly anxious and nervous......I don't think that my body needs any boost to my norepinephrine.

adding the cellcept would be to try and lower the prograf concurrently

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.

These have all been coming and going every day along with a temp that just before taking my CellCept will be around 99.2 - 99.6. After taking my medication my temp drops to my normal 96.6 - 97.4 temp range. So I guess that means the CellCept is suppressing my immune system? LOL.

Right now my doc is tring Cellcept. The jury is still out. But I have been on steroids, Plaquenil, Arava, Methotrexate and now Cellcept.

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.

Cellcept and mg

Common Questions and Answers about Cellcept and mg

cellcept