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imuran
Hi everyone. I was started on Imuran for autoimmune inflammatory arthritis in july. I was tolerating it fine just slight nausea the first day. 3 weeks later I had to stop it because I got a bad UTI. So a week after finishing the antibiotics I re started imuran, 3 hours after taking it I vomited
Hi everyone. I was started on Imuran for autoimmune inflammatory arthritis in july. I was tolerating it fine just slight nausea the first day. 3 weeks later I had to stop it because I got a bad UTI. So a week after finishing the antibiotics I re started imuran, 3 hours after taking it I vomited
Nellies47
in
NRAS
2 years ago
Rituxmab
I have RA with ana (+). Went on orencia and it's not working anymore. Rhemuy wants to stop orencia and start rituximab. I'm wondering if you guys can talk about your experience with the Rituximab.I know everyone's experiences are different on different biologics. I'm also wondering why I wasn't
I have RA with ana (+). Went on orencia and it's not working anymore. Rhemuy wants to stop orencia and start rituximab. I'm wondering if you guys can talk about your experience with the Rituximab.I know everyone's experiences are different on different biologics. I'm also wondering why I wasn't
Avi2013
in
NRAS
2 years ago
Chronic gout after transplant
Hello everyone. I have kidney transplanted 32 years ago. I am suffering from gout attack pretty much right after transplant and until today. My doctor prescribes Allopurinol in a very small dosage because it interacts with Imuran. I like to know if anyone has KRYSTEXXA infusion treatment to reduce
Hello everyone. I have kidney transplanted 32 years ago. I am suffering from gout attack pretty much right after transplant and until today. My doctor prescribes Allopurinol in a very small dosage because it interacts with Imuran. I like to know if anyone has KRYSTEXXA infusion treatment to reduce
nlee
in
Kidney Transplant
2 years ago
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Immunologist referral
Hi everyone. Sorry a bit long winded.🥺 Recently I have developed reactions to medication. In January I developed rash to my HRT patch that I had been using for 6months, then an allergy to my perfume. In Feb I started on methotrexate for my arthritis but I got really bad nausea that lasted 4 weeks, then
Hi everyone. Sorry a bit long winded.🥺 Recently I have developed reactions to medication. In January I developed rash to my HRT patch that I had been using for 6months, then an allergy to my perfume. In Feb I started on methotrexate for my arthritis but I got really bad nausea that lasted 4 weeks, then
Nellies47
in
NRAS
2 years ago
Imuran
How are users fairing on Imuran. I have just started it.
How are users fairing on Imuran. I have just started it.
Goinglong10
in
LUPUS UK
2 years ago
Vaccine & flare
I had Pfizer covid vaccines and my behcets flare came on with a fury. I had been quiet for over 2 years. Anyone else getting the mRNA vaccines have the same problem? Just finally getting back under control with increased Revlimid & Imuran ( along with Rituxan infusions)
I had Pfizer covid vaccines and my behcets flare came on with a fury. I had been quiet for over 2 years. Anyone else getting the mRNA vaccines have the same problem? Just finally getting back under control with increased Revlimid & Imuran ( along with Rituxan infusions)
Expectthebest
in
Behçet's UK
3 years ago
Non-infection with Low-grade fever
Is it common for SLE Lupus patients to have a low-grade fever without an infection? Been on antibiotics (Levofloxacin) for 2 weeks followed by a treatment for yeast infection. I was on 20 mg of prednisone, 200 mg of hydroxchloroquine and 100 mg of imuran at that time, yet I am experiencing the fever.
Is it common for SLE Lupus patients to have a low-grade fever without an infection? Been on antibiotics (Levofloxacin) for 2 weeks followed by a treatment for yeast infection. I was on 20 mg of prednisone, 200 mg of hydroxchloroquine and 100 mg of imuran at that time, yet I am experiencing the fever.
UKMoss
in
LUPUS UK
3 years ago
A Measure of Health with SLE Lupus
Am a 64 year old female diagnosed with SLE Lupus in the June 2000 at age 43, after 2 years of marriage. It affected my left lung (pulmonary fibrosis--doctors were preparing me for a lung transplant but refused it). At this time I was being treated with cyclosporine in preparation for the transplant
Am a 64 year old female diagnosed with SLE Lupus in the June 2000 at age 43, after 2 years of marriage. It affected my left lung (pulmonary fibrosis--doctors were preparing me for a lung transplant but refused it). At this time I was being treated with cyclosporine in preparation for the transplant
UKMoss
in
LUPUS UK
3 years ago
Anyone have any thoughts on being on Prednisone for life, as a second immunosuppressant medication?
I have joined as a concern spouse. My fiancé had a transplant in 2019, he has been taking his medication diligently, however, for the past 8 - 9 months he has been experiencing diarrhea, to a point where he has lost 30 lbs and continues to lose weight. Can anyone speak on the medication of Prednisone
I have joined as a concern spouse. My fiancé had a transplant in 2019, he has been taking his medication diligently, however, for the past 8 - 9 months he has been experiencing diarrhea, to a point where he has lost 30 lbs and continues to lose weight. Can anyone speak on the medication of Prednisone
Thumperet
in
Kidney Transplant
3 years ago
I need an advice regarding medication switch to methotrexate
Hey there guys. Just before I begin to describe my situation, my diagnosis is ANCA vasculitis, which I am fully aware is different from RA yet my treatment is extremely similar and my disease is very rare from what I gathered so I came to this group. I also go to rheumatologist, I'm in my early 20s,
Hey there guys. Just before I begin to describe my situation, my diagnosis is ANCA vasculitis, which I am fully aware is different from RA yet my treatment is extremely similar and my disease is very rare from what I gathered so I came to this group. I also go to rheumatologist, I'm in my early 20s,
Inthegy
in
NRAS
3 years ago
VM AGAIN ?????? 😩
The doctors have given me
IMIGRAN
, but I still have the head pains and constant headache , any advice ???? Thank u all X
The doctors have given me
IMIGRAN
, but I still have the head pains and constant headache , any advice ???? Thank u all X
Debcorn
in
Meningitis Now
3 years ago
RITUXIMAB INFUSION FOR LUPUS AND SJOGRENS
Hi all, Just wondering if anyone found Rituximab good for symptoms of Lupus and skin Lupus And Sjogrens. I had 2 Infusions last month. I was taken off Methotexrate after 9 months due to side effects. Went on Imuran for 7 weeks but unfortunately ended up in hospital with liver damage. I was taken off
Hi all, Just wondering if anyone found Rituximab good for symptoms of Lupus and skin Lupus And Sjogrens. I had 2 Infusions last month. I was taken off Methotexrate after 9 months due to side effects. Went on Imuran for 7 weeks but unfortunately ended up in hospital with liver damage. I was taken off
Haired
in
LUPUS UK
3 years ago
Positive anti chromatin and anti histones
I was diagnosed with lupus about 3.5 years ago, after suffering for 6 years prior. My family dr was treating me for fibromyalgia with little relief, and I asked to be sent to a rheumatologist. The rheumatologist did a bunch of tests and found my ANA was positive, along with a positive anti chromatin
I was diagnosed with lupus about 3.5 years ago, after suffering for 6 years prior. My family dr was treating me for fibromyalgia with little relief, and I asked to be sent to a rheumatologist. The rheumatologist did a bunch of tests and found my ANA was positive, along with a positive anti chromatin
Jodirae
in
LUPUS UK
3 years ago
RITUXAN ANY ADVICE/ COMMENTS ON SIDE EFFECTS
Hi, Anyone got advice on RITUXAN Infusion / Injections. I have Lupus and Sjogrens not have any success with medications. Medication sensitive last two meds Methotrexate health deteriorate over 8 months. Imuran caused liver problems just out of hospital. Taken off Imuran and Mepacrine. Due to see consultant
Hi, Anyone got advice on RITUXAN Infusion / Injections. I have Lupus and Sjogrens not have any success with medications. Medication sensitive last two meds Methotrexate health deteriorate over 8 months. Imuran caused liver problems just out of hospital. Taken off Imuran and Mepacrine. Due to see consultant
Haired
in
LUPUS UK
3 years ago
Reinttoducing Azathioprine/Imuran
Hi, I have taken Imuran/azathioprine for 3 years for my autoinflammatory condition and felt 100% better. YMe and my doctor decided I could then stop the medication. I kept feeling no symptoms for extra 3 years after stopping Imuran. This year I started to flare again. I am back on Imuran for now almost
Hi, I have taken Imuran/azathioprine for 3 years for my autoinflammatory condition and felt 100% better. YMe and my doctor decided I could then stop the medication. I kept feeling no symptoms for extra 3 years after stopping Imuran. This year I started to flare again. I am back on Imuran for now almost
RenataS
in
Crohn's and Colitis Support
3 years ago
what to do when treatments don't work and I keep developing new autoimmune conditions
I am new here so I hope I am posting this correctly! I apologize in advance if I am in the wrong place. I am a 43 year old man who is raising 2 kids alone. After battling 10 years with various symptoms such as fatigue, mental drain and memory issues, pain in joints, frequent falling, etc. I was finally
I am new here so I hope I am posting this correctly! I apologize in advance if I am in the wrong place. I am a 43 year old man who is raising 2 kids alone. After battling 10 years with various symptoms such as fatigue, mental drain and memory issues, pain in joints, frequent falling, etc. I was finally
TiredNerd
in
NRAS
3 years ago
Mycophenolate effects
Hi, I have posted before last year. I live in Ireland but this site is excellent. I was diagnosed with Wegeners/GPA exactly ten years ago - very severe in sinuses and lungs, induced for 18 days. Negligible renal effect but flared in my kidneys in spring last year i.e. 2019. My renal/vasculitis consultant
Hi, I have posted before last year. I live in Ireland but this site is excellent. I was diagnosed with Wegeners/GPA exactly ten years ago - very severe in sinuses and lungs, induced for 18 days. Negligible renal effect but flared in my kidneys in spring last year i.e. 2019. My renal/vasculitis consultant
Corcaigh
in
Vasculitis UK
3 years ago
CHANGED IN MEDICATION - IMURAN
Hi, Had to come off Methotrexate as the side effect were so bad. Now on Imuran but skin burning and rash has started again and is spreading rapidly. Has anyone tried Imuran would appreciate your comments. Thank you and stay safe. Marian
Hi, Had to come off Methotrexate as the side effect were so bad. Now on Imuran but skin burning and rash has started again and is spreading rapidly. Has anyone tried Imuran would appreciate your comments. Thank you and stay safe. Marian
Haired
in
LUPUS UK
4 years ago
Should I go for splenectomy?
Hello I am 28 years old male. I was diagnosed with ITP 4 months ago. I started Prednisone (corticosteroid) and after no response, I started Imuran (immunosuppressants). My platelet count is still less than 10,000. I have no active bleeding also not have any other issue, but have some petechiae on legs
Hello I am 28 years old male. I was diagnosed with ITP 4 months ago. I started Prednisone (corticosteroid) and after no response, I started Imuran (immunosuppressants). My platelet count is still less than 10,000. I have no active bleeding also not have any other issue, but have some petechiae on legs
fooka
in
ITP Support Association
4 years ago
Sitting Pain
I am 51 and was diagnosed at Mayo in January, after two years of multiple orthopedic docs, two spine surgeons, two pain clinics, various injections, a local rheumatologist who told me to get on with life (a female, surprisingly), an internist who wanted to send me to a month-long mental camp, and a boss
I am 51 and was diagnosed at Mayo in January, after two years of multiple orthopedic docs, two spine surgeons, two pain clinics, various injections, a local rheumatologist who told me to get on with life (a female, surprisingly), an internist who wanted to send me to a month-long mental camp, and a boss
Rooney07
in
PMRGCAuk
4 years ago
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