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Hi , looking for some advice have been having a really bad flare for the past three weeks , doctors have put me on 60 mg of predisilone which normally works , but have not yet made a difference I take 3g of
cellcept
a day and 49mg of Humira fortnightly.
Hi , looking for some advice have been having a really bad flare for the past three weeks , doctors have put me on 60 mg of predisilone which normally works , but have not yet made a difference I take 3g of
cellcept
a day and 49mg of Humira fortnightly.
Hidden
in
Behçet's UK
6 years ago
Moving from US to UK with Lupus
I am currently taking levothyroxine sodium, plaquenil, and
cellcept
. Any help or information will be helpful before we decide to move forward with this. Thank you so much in advance.
I am currently taking levothyroxine sodium, plaquenil, and
cellcept
. Any help or information will be helpful before we decide to move forward with this. Thank you so much in advance.
Iris365
in
LUPUS UK
6 years ago
Tacrolimus?
Chloroquine,
Cellcept
, Azathioprine, one dose of Rituximab. Now starting on Tacrolimus but worried about long term. Anyone else?
Chloroquine,
Cellcept
, Azathioprine, one dose of Rituximab. Now starting on Tacrolimus but worried about long term. Anyone else?
patient165
in
LUPUS UK
6 years ago
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Purple striae/stretchmarks?
😩 My lupie meds: Calcium and vit D Hydroxychloroquine Prednisolone 10 mg
CellCept
1000 mg BD
😩 My lupie meds: Calcium and vit D Hydroxychloroquine Prednisolone 10 mg
CellCept
1000 mg BD
ellejay46
in
LUPUS UK
6 years ago
Cellcept and white blood count
My
cellcept
blood got taken and my white count is sitting at 2.9...I'm the winter it dropped to 1.3...I don't want that happening again! Is this a sign that
Cellcept
is no longer an opt option for me? Been on 750xtwice daily
My
cellcept
blood got taken and my white count is sitting at 2.9...I'm the winter it dropped to 1.3...I don't want that happening again! Is this a sign that
Cellcept
is no longer an opt option for me? Been on 750xtwice daily
curran61
in
LUpus Patients Understanding and Support
6 years ago
Mycophenolate update after Rheumy appt
She said she could put me back on Myco in the form of
Cellcept
, but not until I trialled time off it. I get this, I really do. But the thing is (and I did not say this aloud) my sister is coming to stay with me for a month next week from Canada.
She said she could put me back on Myco in the form of
Cellcept
, but not until I trialled time off it. I get this, I really do. But the thing is (and I did not say this aloud) my sister is coming to stay with me for a month next week from Canada.
panda2
in
LUPUS UK
6 years ago
Help!!
Im taking 17.5 mg of prednisilone having had to to stop
Cellcept
due to infection. Due to see rheumatologist in 2 days. Can anyone help please
Im taking 17.5 mg of prednisilone having had to to stop
Cellcept
due to infection. Due to see rheumatologist in 2 days. Can anyone help please
Bronn
in
LUPUS UK
6 years ago
Sun, sea, SI joints and Cellcept
I wonder if any of you have experienced general improvement while on
Cellcept
. I'd also appreciate any input regarding SI joint issues as I'm curious to know if physio has helped you at all.
I wonder if any of you have experienced general improvement while on
Cellcept
. I'd also appreciate any input regarding SI joint issues as I'm curious to know if physio has helped you at all.
flap7
in
LUPUS UK
6 years ago
10 months post transplant recipient...side effects
I'm on prograf,
cellcept
and 5mg prednisone. Sleeping for the most part is pretty good. I do have nights where I can't sleep, but mostly I can sleep.
I'm on prograf,
cellcept
and 5mg prednisone. Sleeping for the most part is pretty good. I do have nights where I can't sleep, but mostly I can sleep.
Jenny0604
in
Kidney Transplant
6 years ago
Newbie with drug question
I have been on plaquenil (continues,) Rituxan, Prednisone, and
Cellcept
(generic). I have a bevy of symptoms: joint and muscle pain, vision problems, impaired brain function and memory issues, headaches, flushing, rash, hives, nerve pain (primarily in my feet), and hair loss.
I have been on plaquenil (continues,) Rituxan, Prednisone, and
Cellcept
(generic). I have a bevy of symptoms: joint and muscle pain, vision problems, impaired brain function and memory issues, headaches, flushing, rash, hives, nerve pain (primarily in my feet), and hair loss.
WordWeaver
in
LUPUS UK
6 years ago
Pain in hands - advagraf & cellcept
I take advagraf and
cellcept
. Does anyone else suffer from anything similar?
I take advagraf and
cellcept
. Does anyone else suffer from anything similar?
Isabelle2
in
British Liver Trust
6 years ago
Creatinine levels going up after 4 weeks on cellcept and prednisone and 3 iv infusions...anyone with similar experience?
Since starting his meds
cellcept
2g and prednisone 20mg his creatinine levels have gone upwards, so has just done IV steroids for 3 days and tomorrow begins 60mg prednisone. His creatinine today was up to 335! We don’t understand why it is going up ? Any ideas ?
Since starting his meds
cellcept
2g and prednisone 20mg his creatinine levels have gone upwards, so has just done IV steroids for 3 days and tomorrow begins 60mg prednisone. His creatinine today was up to 335! We don’t understand why it is going up ? Any ideas ?
C17ley
in
LUPUS UK
6 years ago
Clinical Trials
Back then, at U of WI they put transplant patients on Neoral and
Cellcept
.
Cellcept
really had some bad side effects for your gastrointestinal tract. Many transplant recipients wound up with ulcers and some had daily diarrhea.
Back then, at U of WI they put transplant patients on Neoral and
Cellcept
.
Cellcept
really had some bad side effects for your gastrointestinal tract. Many transplant recipients wound up with ulcers and some had daily diarrhea.
WYOAnne
NKF Ambassador
in
Kidney Transplant
6 years ago
9 months post kidney transplant...side effects are changing
I'm also on
Cellcept
which doesn't seem to bother me as much. Thanks!
I'm also on
Cellcept
which doesn't seem to bother me as much. Thanks!
Jenny0604
in
Kidney Transplant
6 years ago
Streptycoccal pneumonia
Has anyone else had this and re attempted
cellcept
after?
Has anyone else had this and re attempted
cellcept
after?
Joanna36
in
LUPUS UK
6 years ago
Autoimmunity and eds
I had taken steroids and started
cellcept
then within weeks became very ill and my immune system severely attacked my face and neck and he's in somehow. I feel labotomised tbh. It turns out I've had strepyococcal pneumonia. So I've had to stop
cellcept
.
I had taken steroids and started
cellcept
then within weeks became very ill and my immune system severely attacked my face and neck and he's in somehow. I feel labotomised tbh. It turns out I've had strepyococcal pneumonia. So I've had to stop
cellcept
.
Joanna36
in
Ehlers-Danlos Support UK
6 years ago
Skin Problems - are these serious or what?
Take Plaquenil,
Cellcept
- I can't stand all this and not feeling better - always these rashes and welts coming out, then it goes away, I use Cortizone cream and Aveeno to soothe it a little - changed to Dove soap.
Take Plaquenil,
Cellcept
- I can't stand all this and not feeling better - always these rashes and welts coming out, then it goes away, I use Cortizone cream and Aveeno to soothe it a little - changed to Dove soap.
fruzsi01
in
LUPUS UK
6 years ago
Agonising pain after steroid taper
I had started
cellcept
4 kweeks ago. I went to a and e last night as felt something was eating me alive. If course they sent me home as have no temperature. Has anyone has this after steroid taper. Makes me think it wasn't worth it as feel so horrificly worse now.
I had started
cellcept
4 kweeks ago. I went to a and e last night as felt something was eating me alive. If course they sent me home as have no temperature. Has anyone has this after steroid taper. Makes me think it wasn't worth it as feel so horrificly worse now.
Joanna36
in
LUPUS UK
7 years ago
What about the AQP4 antibody? Just another twist in this sordid tale to diagnosis...
NMO is treated more aggressively and with many of the same drugs (
cellcept
/mm, azathioprine, rituximab). But, if you have an acute attack it requires 5 days of MP I.V. or plasmapheresis. I'm just feeling a bit out of sorts.
NMO is treated more aggressively and with many of the same drugs (
cellcept
/mm, azathioprine, rituximab). But, if you have an acute attack it requires 5 days of MP I.V. or plasmapheresis. I'm just feeling a bit out of sorts.
DRunnerchick
in
LUPUS UK
6 years ago
Upper back pain
I have scleroderma which includes lung involement & Raynaud’s and currently take
cellcept
. I recently had the awful virus which lasted about 5 weeks and i am still coughing. I had a chest x-ray the other day which came back clear.
I have scleroderma which includes lung involement & Raynaud’s and currently take
cellcept
. I recently had the awful virus which lasted about 5 weeks and i am still coughing. I had a chest x-ray the other day which came back clear.
NSV69
in
Scleroderma & Raynaud's UK (SRUK)
7 years ago
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