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CellCept
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Painkillers? Any suggestions?
I am currently on Predisolone,
Cellcept
and Methotrexate. I thought I was getting better, but then I notice about 3 new flare ups on my feet. Which instantly got me depress. It is really difficult to deal with the pain when I'm at work. Its really hard, I was taking pethidine.
I am currently on Predisolone,
Cellcept
and Methotrexate. I thought I was getting better, but then I notice about 3 new flare ups on my feet. Which instantly got me depress. It is really difficult to deal with the pain when I'm at work. Its really hard, I was taking pethidine.
Hanna22
in
Vasculitis UK
12 years ago
Reducing cellcept - is there anything I need to know
I saw my consultant on Thurs and as my bloods have been stable, he wants me to reduce my
cellcept
doses slowly. Is there any withdrawal symptoms in reducing immunosupressant drugs? Any advice would be great.
I saw my consultant on Thurs and as my bloods have been stable, he wants me to reduce my
cellcept
doses slowly. Is there any withdrawal symptoms in reducing immunosupressant drugs? Any advice would be great.
KTWells
in
Vasculitis UK
12 years ago
Fatigue. Why are some days better than others? Is this normal?
Also, I'm on prednisone,
cellcept
and urso - can any of these drugs make you feel fatigued? Thanks! Karen
Also, I'm on prednisone,
cellcept
and urso - can any of these drugs make you feel fatigued? Thanks! Karen
KarenRL
in
PBC Foundation
12 years ago
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Is anyone taking Cellcept? How many mg. a day are you taking? What shape are your lungs in? Have you suffered any side effects?
joba
in
Scleroderma & Raynaud's UK (SRUK)
12 years ago
Some Good News at Last!
I attended my appointment yesterday with My Rheum Consultant and after he increased my
CellCept
or MMF wef 17th May, ( I am now on 2000mg per day), my Lupus levels and immune system is now back in the black.
I attended my appointment yesterday with My Rheum Consultant and after he increased my
CellCept
or MMF wef 17th May, ( I am now on 2000mg per day), my Lupus levels and immune system is now back in the black.
Lulabelle
in
LUPUS UK
12 years ago
Hia, I'm new to site and Behcet's. Been reading blogs. As it's been helpful I'm venturing a question! Anyone taken CellCept (Mycophenolate)?
I've been taking for months now but it doesn't feel like it's making a difference. Consultant says to give it time, but not giving an indication of how long. I was diagnosed in Sep 2011 and steroids made a quick improvement. I then went on azathioprine and was able to reduce steroids. I really felt a
I've been taking for months now but it doesn't feel like it's making a difference. Consultant says to give it time, but not giving an indication of how long. I was diagnosed in Sep 2011 and steroids made a quick improvement. I then went on azathioprine and was able to reduce steroids. I really felt a
Godles
in
Behçet's UK
12 years ago
Just wondering how long after starting steriods did your ALT begin to drop?
I've been taking prednisone,
cellcept
and urso (I have AIH/PBC Overlap) for two months and my ALT is rising. Is this typical or is the treatment not working?
I've been taking prednisone,
cellcept
and urso (I have AIH/PBC Overlap) for two months and my ALT is rising. Is this typical or is the treatment not working?
KarenRL
in
British Liver Trust
12 years ago
Low blood count
I am on mycophenate motofil (
Cellcept
) and mepacrine. I feel ok except from being really tired which I've put down to other medication. She is chasing up my rhuemie appointment but I wondered what do they do in these circumstances? Thank you.
I am on mycophenate motofil (
Cellcept
) and mepacrine. I feel ok except from being really tired which I've put down to other medication. She is chasing up my rhuemie appointment but I wondered what do they do in these circumstances? Thank you.
KTWells
in
Vasculitis UK
12 years ago
Liver Pain - Due to medications or is condition worsening?
I'm wondering if anyone can tell me if this is likely a sign that my condition is worsening or could it be due to the medications I am now taking (prednisone,
cellcept
and urso). Has anyone else experienced this?
I'm wondering if anyone can tell me if this is likely a sign that my condition is worsening or could it be due to the medications I am now taking (prednisone,
cellcept
and urso). Has anyone else experienced this?
KarenRL
in
PBC Foundation
12 years ago
HOLIDAYS ABROAD ?
However, since my Lupus has been confirmed just over 12 months ago and because of the
Cellcept
or MMF medication. (it states to keep out of the sun).
However, since my Lupus has been confirmed just over 12 months ago and because of the
Cellcept
or MMF medication. (it states to keep out of the sun).
Lulabelle
in
LUPUS UK
12 years ago
Vasculitis reaction-couldn't move legs
Just to note I am currently tapering down
cellcept
(from 2000mg per day -0mg) for Rutiximab treatment in 10 days time but also on 40 mg preds, 540 mg Fexofenadine, 10 mg Ivabravadine, 10 mg Singulair, 15 mg Lansoprazole, 24 mg Piriton, Adcal-3, 5mg Diazepam, Alendronic Acid (once per week).
Just to note I am currently tapering down
cellcept
(from 2000mg per day -0mg) for Rutiximab treatment in 10 days time but also on 40 mg preds, 540 mg Fexofenadine, 10 mg Ivabravadine, 10 mg Singulair, 15 mg Lansoprazole, 24 mg Piriton, Adcal-3, 5mg Diazepam, Alendronic Acid (once per week).
Sarahjh2004
in
Vasculitis UK
12 years ago
Is anybody taking Mycophenolate Mofetil (MMF) ?
We've been asked about people's experiences taking MMF
Cellcept
. If you have taken it could you please share? Thank you.
We've been asked about people's experiences taking MMF
Cellcept
. If you have taken it could you please share? Thank you.
Paul_Howard
LUPUS UK
in
LUPUS UK
12 years ago
Help with Medication Queries? New to this board!
He mentioned that once I have been on 5mg for a couple of months and if my immune system has calmed or gone back into remission, that my
Cellcept
will be increased by a further 500mg for a further couple of weeks/months.
He mentioned that once I have been on 5mg for a couple of months and if my immune system has calmed or gone back into remission, that my
Cellcept
will be increased by a further 500mg for a further couple of weeks/months.
Lulabelle
in
LUPUS UK
12 years ago
Seen this on the internet - positive as it Highlights Lupus. Men may find this useful with Lupus SLE
Immunosuppressive drugs may also be used (with or in place of steroid treatments), such as cyclophosphamide (Cytoxan®), azathioprine (Imuran®), cyclosporin A, and mycophenolate mofetil (
CellCept
®).
Immunosuppressive drugs may also be used (with or in place of steroid treatments), such as cyclophosphamide (Cytoxan®), azathioprine (Imuran®), cyclosporin A, and mycophenolate mofetil (
CellCept
®).
Lulabelle
in
LUPUS UK
12 years ago
Severe asthma - Unconventional Treatment
I am on every asthma medication available, including at least 40 mg of prednisone a day, xolair, and ivig. my docs are now suggesting trying more aggresive treatments, as my pft's are slowly drifting down and begining to become irreversible. they are suggesting
cellcept
, and antirejection drug, or even
I am on every asthma medication available, including at least 40 mg of prednisone a day, xolair, and ivig. my docs are now suggesting trying more aggresive treatments, as my pft's are slowly drifting down and begining to become irreversible. they are suggesting
cellcept
, and antirejection drug, or even
Hidden
in
Asthma Community Forum
17 years ago
Rituxan -v- Clinical Trials - The option given to me yesterday, Please HELP! me?
Lately Methotrexate was stopped and Mycophenolate (
Cellcept
) 1500mg daily introduced in March 11. I had my first Lupus flare in March 2009 after returning from holiday in the Caribbean. Since these flare started its been impossible to get any long term relieve from lupus.
Lately Methotrexate was stopped and Mycophenolate (
Cellcept
) 1500mg daily introduced in March 11. I had my first Lupus flare in March 2009 after returning from holiday in the Caribbean. Since these flare started its been impossible to get any long term relieve from lupus.
Glen1
in
LUPUS UK
12 years ago
Peripheral Neuropathy
I am currently being weaned off
Cellcept
and steroids and the pain in my feet has returned alongside very itchy eyebrows! I am being sent for nerve tests but apparently these are both signs of Peripheral Neuropathy common amongst MPA patients. Anyone else experiencing this?
I am currently being weaned off
Cellcept
and steroids and the pain in my feet has returned alongside very itchy eyebrows! I am being sent for nerve tests but apparently these are both signs of Peripheral Neuropathy common amongst MPA patients. Anyone else experiencing this?
Jackie29
in
Vasculitis UK
12 years ago
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