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When using Cellcept..what do they look for in your blood work? is it like

Imuran? they have to

make sure it doesn't become toxic to your liver? or is it something else?

I was just wondering...being on the Prednisone and the imuran..if it ever became

a

problem..that could be a alternative.

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On Sat, 18 Jun 2005 19:40 , 'bursten1948' <bubblesburstin@...> sent:

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>I was also put on Cellcept since my genetic makeup would not allow me

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>to take Imuran.  I stopped it after a short time because there was a

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>dispute on what my diagnosis was and still is.  I then had another

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>liver biopsy and still do not have a definite diagnosis.  Two docs

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>think I have PBC and two think I have AIH.  I think that I have both.

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> Anyway, I am about ready to start back on the Cellcept.  I did not

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>have any problems with it before.  I also am on Urso and some of my

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>liver tests have come down.  I am seeing my liver doc in 3 weeks to

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>discuss adding the cellcept to my therapy.  It just seemed like and

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>awfully powerful drug to be using and it scared me.  I guess I am now

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>resigned to the fact that I need these drugs and better get on them ASAP.

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  • 9 months later...
Guest guest

Prednisone can also cause acne. I take prednisone 10/5mg alternate at 50mg

imuran.

[ ] CellCept

Devon

I take CellCept. Have been on it for about 6 months. Dont really have

any side effects from it. Except maybe acne. I also take Prednisone

25mg. It is kinda difficult to know if a drug works when taking

prdnisone because it is the main drug. But I guess it is. Still trying

to get my Hep. Dr.to decrease my Prednisone. Then I will know for sure.

I also have a correction in my last post. I said I take CellCept

2000mg twice a day and it is 1000mg twice a day. Sorry for the miss

type

Connie

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  • 9 months later...

Have you discussed this decision, and its implications, with your doctor?

Is Cellcept a drug that you can go on and off without problems?

I've never taken Cellcept, only Prednisone and Azathioprine. However, my

guess is that it's like that drug program in that you must follow it exactly as

prescribed.

Bear in mind that the death rate for AIH not responsive to treatment are a

lot worse, a whole lot worse, than a 1% lymphoma occurrence.

Harper

In a message dated 1/12/07 9:56:15 AM, helsusac@... writes:

> I was on Cellcept 250 mg twice a day and had no problems. As my LFT's were

> still sllighlty high AST 100 ALT 65 or visa versa, my doctor upped it to 500

> mg twice a day. After the first day I developed a sore throat which is one of

> the side effects listed on the brochure that comes from the pharmacy with my

> medication. I decided I'll go off of it for a week and heal the throat and

> then try again, as the sore throat could be caused by something else. Did

> anyone else have a problem like this? Also the brochure mentioned lymphoma,

which

> is pretty scary--does anyone know the statistics of how often that happens.

> I would feel a lot better if it was 1% or less.

>

> Helene

>

>

>

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I was on Cellcept 250 mg twice a day and had no problems. As my LFT's were

still sllighlty high AST 100 ALT 65 or visa versa, my doctor upped it to 500 mg

twice a day. After the first day I developed a sore throat which is one of the

side effects listed on the brochure that comes from the pharmacy with my

medication. I decided I'll go off of it for a week and heal the throat and then

try again, as the sore throat could be caused by something else. Did anyone

else have a problem like this? Also the brochure mentioned lymphoma, which is

pretty scary--does anyone know the statistics of how often that happens. I

would feel a lot better if it was 1% or less.

Helene

AZ PBC 1/AIH 2/6 Grade 5 out of 18

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  • 5 months later...
Guest guest

Kerri,

I took CellCept for a very short period about a year ago. This

was due to the fact that it was ineffective for me. I don't remember

any side effects, although I do remember that it had to be taken a few

hours before and after eating anything else, which was difficult for me

because of all the other medications I take throughout the day.

I hope your son has better results. I know that others take

CellCept and I hope they will respond.

Sharon

>

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Kerri,

My daughter(16) has been on Cellcept for 2 years now. She takes 1000mg/day.

She started on Imuran and after 4 months her labs went crazy. There is a blood

test that can predict whether imuran can be processed in a person's body. Her

results showed that her body could not process imuran and in fact her GGT

numbers were so out of line they considered her toxic. So far, she has no side

effects from the Cellcept and her labs have pretty much been in normal range.

She currently takes 1mg of prednisone(down from 40mg last July) 1800mg of

Urso(for PSC diagnosis), 1000 mg of Cellcept, muti vitamin, extra calcium and

fish oil. I am so happt to say she is doing very well although I still hold my

breath every 2 weeks when we go for lab work. I have no concern or the Cellcept

it is the prednisone that we continue to want decreased.

mom to Caity(16) AIH/PSC 1/05

---------------------------------

Fussy? Opinionated? Impossible to please? Perfect. Join 's user panel and

lay it on us.

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Guest guest

Thank you so much for your response.  I am hopeful that the cellcept will help

us to wean my son off of his prednisone too.  He is currently taking only 6 mg,

but when we dropped it below that, his polyneuropathy returned.  Luckily his

liver numbers have remained good though.  I am not sure what dosage he will be

on, but he is only 4 years old and only weighs about 28 pounds, so he won't be

on too big a dose to start.  Thanks again for your response.

Re: [ ] Cellcept

Kerri,

My daughter(16) has been on Cellcept for 2 years now. She takes 1000mg/day. She

started on Imuran and after 4 months her labs went crazy. There is a blood test

that can predict whether imuran can be processed in a person's body. Her results

showed that her body could not process imuran and in fact her GGT numbers were

so out of line they considered her toxic. So far, she has no side effects from

the Cellcept and her labs have pretty much been in normal range. She currently

takes 1mg of prednisone(down from 40mg last July) 1800mg of Urso(for PSC

diagnosis), 1000 mg of Cellcept, muti vitamin, extra calcium and fish oil. I am

so happt to say she is doing very well although I still hold my breath every 2

weeks when we go for lab work. I have no concern or the Cellcept it is the

prednisone that we continue to want decreased.

mom to Caity(16) AIH/PSC 1/05

---------------------------------

Fussy? Opinionated? Impossible to please? Perfect. Join 's user panel and

lay it on us.

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  • 11 months later...
Guest guest

You sound like you have aquired the skill of living! Good for you! It sounds

wonderful,you in the garden with a good book, watching the birdsand listening

to their sounds.

I like gardening too, or rather I like to have my garden in order and looking

good. I love flowers and cutting the irises and daffodils and other flowering

plants always lifts my spirit. Even in the winter I buy flowers for my table.

Thanks for sharing a moment of tranquility!

Clara from OR.'dx99

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  • 1 year later...

Liljoejoe, I was on Cellcept post transplant for years........am now off and

only take the cyclosporin. But, I had no trouble with the Cellcpet after my

initial start on it.  After a few months I had no side effects at all.......good

luck.  Joanne

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