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CellCept
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Complicated case. . . .
I was changed from
cellcept
to everolimus to help with painful diarrhea and also to start the weaning process of the prednisone.
I was changed from
cellcept
to everolimus to help with painful diarrhea and also to start the weaning process of the prednisone.
sdahnke
in
Anticoagulation Support
10 years ago
Lupus flare up
(on
Cellcept
.) Many thanks.
(on
Cellcept
.) Many thanks.
tillie
in
LUPUS UK
9 years ago
CLL and curly hair
Only noticeable side effects-occasional night cramps, fingernails splitting, bruising (also taking 500mgX2
Cellcept
) and my hair which has gone from poker straight to very wavy/curly in the last two months. Alarming, but puzzling. Anyone else experiencing similar "hair raising" side effects?
Only noticeable side effects-occasional night cramps, fingernails splitting, bruising (also taking 500mgX2
Cellcept
) and my hair which has gone from poker straight to very wavy/curly in the last two months. Alarming, but puzzling. Anyone else experiencing similar "hair raising" side effects?
Villager
in
CLL Support
10 years ago
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Hi, I have scleroderma among other things. The most concerning of which is lung fibrosis.
After consultations between my 2 consultants, (chest and rheumatology), they have decided to prescribe me Mycophenolate Mofetil (
CellCept
). I have 100% trust in my medical advisors, however, I read with trepidation the 8 page accompanying document about possible side effects.
After consultations between my 2 consultants, (chest and rheumatology), they have decided to prescribe me Mycophenolate Mofetil (
CellCept
). I have 100% trust in my medical advisors, however, I read with trepidation the 8 page accompanying document about possible side effects.
titanicus
in
Lung Conditions Community Forum
10 years ago
Gastric Ulcers
I didn't respond to Aziathiprine, or Mychophenolate (
cellcept
) on this for over 1 year, and I've just started Infiximab infusions. ( I cannot imaging life without suffering from these symptoms, especially the ulcers, but it might happen with the Infliximab :-) ) Another question, is: when a colonoscope
I didn't respond to Aziathiprine, or Mychophenolate (
cellcept
) on this for over 1 year, and I've just started Infiximab infusions. ( I cannot imaging life without suffering from these symptoms, especially the ulcers, but it might happen with the Infliximab :-) ) Another question, is: when a colonoscope
Bethb
in
Behçet's UK
10 years ago
Anyone experiencing chronic low immunoglobulins
infections + comprehensive metabolic bone unit blood tests prior to starting IV osteoporosis treatment that resulted in these insights (my long term chronically low leucocytes, neutrophils & immunoglobulin & IgG, IgA, IgM have gone even lower following 3 1/2 yrs on daily hydroxy 400mg + 1 year on daily myco
cellcept
infections + comprehensive metabolic bone unit blood tests prior to starting IV osteoporosis treatment that resulted in these insights (my long term chronically low leucocytes, neutrophils & immunoglobulin & IgG, IgA, IgM have gone even lower following 3 1/2 yrs on daily hydroxy 400mg + 1 year on daily myco
cellcept
Barnclown
in
LUPUS UK
10 years ago
Missed/ delayed menstrual cycle with MMF (cellcept)
I have had ITP since January last year. My periods started to last about three or four days after high dose dexamethason on and off up until August. I then started a new drug called MMF which is an immunosuppressant. I'm really worried as last month my period was 3 weeks late and this month it hasn't
I have had ITP since January last year. My periods started to last about three or four days after high dose dexamethason on and off up until August. I then started a new drug called MMF which is an immunosuppressant. I'm really worried as last month my period was 3 weeks late and this month it hasn't
Enyacurran
in
ITP Support Association
10 years ago
Me again
Back to square one again una bad way change from asatriopin to
cellcept
mico) and of coarse a bal flare joints ok but chest pain out my shoulders and down my arms rand to see if any one would see me was told go toa&e great help that was didn't go just took more pain killers.
Back to square one again una bad way change from asatriopin to
cellcept
mico) and of coarse a bal flare joints ok but chest pain out my shoulders and down my arms rand to see if any one would see me was told go toa&e great help that was didn't go just took more pain killers.
Limerick5
in
LUPUS UK
10 years ago
Another update
Taking
Cellcept
means I am photosensitive so can't sit in the sun any longer so am actually looking forward to winter drawing nearer, can't believe I am saying that!
Taking
Cellcept
means I am photosensitive so can't sit in the sun any longer so am actually looking forward to winter drawing nearer, can't believe I am saying that!
CDreamer
in
Atrial Fibrillation Support
10 years ago
Cellcept and twitching
Has anyone on
cellcept
experienced twitching? My eye has been twitching intermittently which I could also attribute to allergies. What's more concerning is I feel my head is twitching at times. I'm not sure if it's the
cellcept
, nerves (I'm kind of high strung) or something else.
Has anyone on
cellcept
experienced twitching? My eye has been twitching intermittently which I could also attribute to allergies. What's more concerning is I feel my head is twitching at times. I'm not sure if it's the
cellcept
, nerves (I'm kind of high strung) or something else.
lnselou79
in
LUPUS UK
10 years ago
Hello, I have my first Rituxumab infusion in two weeks, will it be ok to go to a family wedding the next week - its 600 miles from home?
After a year and a half on varying doses of Prednisilone and
Cellcept
(along with a plethora of other 'big guns' for managing BP etc) I have avoided dialysis and am just about to embark on Rituxumab infusions.
After a year and a half on varying doses of Prednisilone and
Cellcept
(along with a plethora of other 'big guns' for managing BP etc) I have avoided dialysis and am just about to embark on Rituxumab infusions.
cloudym
in
LUPUS UK
10 years ago
Starting cellcept (mycophenolate mofetil) , I would love to hear your experience with this.
Do you take it with or without food? Any side effects? If you experience nausea, how long does it normally last after the dose. Any organ involvement?
Do you take it with or without food? Any side effects? If you experience nausea, how long does it normally last after the dose. Any organ involvement?
Cherylv
in
LUPUS UK
10 years ago
Does anyone get meds for hair loss due to the meds like regaine I would think some ladies will but docs tend not to with blokes I think
Cos the
cellcept
seems to make it recede but the consultant is fobbing me off So would like some info to have a heated discuss with
Cos the
cellcept
seems to make it recede but the consultant is fobbing me off So would like some info to have a heated discuss with
glasgowguy
in
LUPUS UK
11 years ago
Anyone on myfortic (mycophenolate sodium)?
I'm in my 3rd month on mycophenolate
cellcept
. I really really like
cellcept
!!!!!
I'm in my 3rd month on mycophenolate
cellcept
. I really really like
cellcept
!!!!!
Barnclown
in
LUPUS UK
11 years ago
has anyone been on cellcept
Seen a kidney doctor he put me on these new tablets called
Cellcept
, is anyone on them or been on them?
Seen a kidney doctor he put me on these new tablets called
Cellcept
, is anyone on them or been on them?
grace1
in
PMRGCAuk
11 years ago
In remission and 2 months without cellcept and on 5mg pronisone.Any experience.
My daughter has pulmo renal syndrome panca and gbm positive . She has been diagnosen 12.2011.She is 2 years in induced remission. Her Dr.decided to stop MMF in 1.2014 afer 18 months.This days she is taking 5mg calcort(pronisone). Any experience about remission and getting off all medicament.
My daughter has pulmo renal syndrome panca and gbm positive . She has been diagnosen 12.2011.She is 2 years in induced remission. Her Dr.decided to stop MMF in 1.2014 afer 18 months.This days she is taking 5mg calcort(pronisone). Any experience about remission and getting off all medicament.
tamidi
in
Vasculitis UK
11 years ago
short term memory
does anybody who takes
cellcept
and prednisolone find they get short term memory problems.
does anybody who takes
cellcept
and prednisolone find they get short term memory problems.
molliecatone
in
Vasculitis UK
11 years ago
Anyone tried Cellcept ( Mykofenolatmofetil ) ?
Now I have a new rheumatologist and he suggested I should try
Cellcept
. When I read what you wright PMRpro I understand that I have reducing Prednisolon to fast from the beginning. I started at 50 mg. It took me four years to come below ten .
Now I have a new rheumatologist and he suggested I should try
Cellcept
. When I read what you wright PMRpro I understand that I have reducing Prednisolon to fast from the beginning. I started at 50 mg. It took me four years to come below ten .
AkselOlsen
in
PMRGCAuk
11 years ago
Anyone with MPA or Wegener and without any imumosupeesant like celcept imuran
My doughter have MPA.She is on
cellcept
for 18 months with pron.She is in remmision.Yesterday dr.told me that he would take she off
cellcept
in another 2 months.She is taking also 20 mg pronisone second day.Any expirience.
My doughter have MPA.She is on
cellcept
for 18 months with pron.She is in remmision.Yesterday dr.told me that he would take she off
cellcept
in another 2 months.She is taking also 20 mg pronisone second day.Any expirience.
tamidi
in
Vasculitis UK
11 years ago
Does any body get the following side effects from Cellcept and prednisolone
I am getting hot flushes though this maybe a coincidence as I am a 47 year old female!!! I am also getting minor shakes mainly in the hands any advice please
I am getting hot flushes though this maybe a coincidence as I am a 47 year old female!!! I am also getting minor shakes mainly in the hands any advice please
molliecatone
in
Vasculitis UK
11 years ago
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