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Rituximab
has anybody experienced flue like symptoms or fevers on
Rituximab
? Or chronic sinusitis?
has anybody experienced flue like symptoms or fevers on
Rituximab
? Or chronic sinusitis?
Johnnyboy66
in
Vasculitis UK
Rituximab and covid
I've been on
Rituximab
successfully for several years now. But since learning that
Rituximab
reduces the impact of covid vaccinations, my rheumatologist is understandably slow to prescribe the next infusion.
I've been on
Rituximab
successfully for several years now. But since learning that
Rituximab
reduces the impact of covid vaccinations, my rheumatologist is understandably slow to prescribe the next infusion.
cathie
in
NRAS
Rituximab
Hallo, is anyone out there on
Rituximab
, or know how successful or not. I’m currently on Methotrexate 25 strength and am concerned Thanks Liz 💕
Hallo, is anyone out there on
Rituximab
, or know how successful or not. I’m currently on Methotrexate 25 strength and am concerned Thanks Liz 💕
Hope164
in
NRAS
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Rituximab and tetanus (etc.)
This is to all my fellow immune suppressed folks about
rituximab
. I've been unable to find solid information, and my consultants aren't sure, so wondered if anyone here knows. Does
rituximab
impact our tetanus jabs and similar?
This is to all my fellow immune suppressed folks about
rituximab
. I've been unable to find solid information, and my consultants aren't sure, so wondered if anyone here knows. Does
rituximab
impact our tetanus jabs and similar?
Grizzly-bear
in
Vasculitis UK
Rituximab
Hi all you lovely people who responded to my question re
Rituximab
, well I have just returned from the hospital and am unable to report how I got on as they didn’t do it !!
Hi all you lovely people who responded to my question re
Rituximab
, well I have just returned from the hospital and am unable to report how I got on as they didn’t do it !!
Lorrayne
in
NRAS
Rituximab
Hi everyone, on Wednesday I have my first
Rituximab
infusion, not sure what to expect, how my body is likely to respond, so any advice or comments would be greatly appreciated. Thankyou
Hi everyone, on Wednesday I have my first
Rituximab
infusion, not sure what to expect, how my body is likely to respond, so any advice or comments would be greatly appreciated. Thankyou
Lorrayne
in
NRAS
Rituximab and evusheld
I’m due to have another infusion of
Rituximab
and May. I just had covid and I was ok. I know after
Rituximab
I will end up with no antibodies. Does anyone know if they are given Evusheld injections in Uk after
Rituximab
infusion? My consultant didn’t know to much about it when I last saw him.
I’m due to have another infusion of
Rituximab
and May. I just had covid and I was ok. I know after
Rituximab
I will end up with no antibodies. Does anyone know if they are given Evusheld injections in Uk after
Rituximab
infusion? My consultant didn’t know to much about it when I last saw him.
JAQUEKB
in
Kidney Disease
An injection of iloprost and rituximab for systemic sclerosis Raynaud's phenomenon
Has anyone received an injection of iloprost and
rituximab
? After it is received, is there any improvement noticed? Also does insurance cover these 2 medicine?
Has anyone received an injection of iloprost and
rituximab
? After it is received, is there any improvement noticed? Also does insurance cover these 2 medicine?
Lo1234
in
Scleroderma & Raynaud's UK (SRUK)
Testing positive for Covid on Ritux
Has anyone on
Rituximab
had Covid and if so how did it go for you?
Has anyone on
Rituximab
had Covid and if so how did it go for you?
Loftyc
in
ITP Support Association
Rituximab and Covid
I asked the Rheumatologist hosting the event about how does
rituximab
affect memory B cells and will my body produce antibodies in the case of a Covid infection.
I asked the Rheumatologist hosting the event about how does
rituximab
affect memory B cells and will my body produce antibodies in the case of a Covid infection.
ks1966
in
NRAS
Caught COVID abroad?
I am immunosuppressed after treatment with
rituximab
and cannot produce antibodies against COVID. I would like to fly home to visit family. Have any of you travelled whilst still immunosuppressed? Has anyone ever caught COVID abroad? What did you do?
I am immunosuppressed after treatment with
rituximab
and cannot produce antibodies against COVID. I would like to fly home to visit family. Have any of you travelled whilst still immunosuppressed? Has anyone ever caught COVID abroad? What did you do?
Tonkotsu
in
LUPUS UK
Rituximab covid19
Has anyone who is on
rituximab
had covid. Have just had first infusion of this cycle and am worried about getting covid at work as so many people have it.
Has anyone who is on
rituximab
had covid. Have just had first infusion of this cycle and am worried about getting covid at work as so many people have it.
jeanette60
in
Arthritis Ireland
sleepy
Can I ask if anyone gets really sleepy when the
Rituximab
is due? My partner is having his next week and for the past couple of weeks he’s slept most of the day. Just wondering if it’s to do with this. Thanks for taking the time to read this x
Can I ask if anyone gets really sleepy when the
Rituximab
is due? My partner is having his next week and for the past couple of weeks he’s slept most of the day. Just wondering if it’s to do with this. Thanks for taking the time to read this x
Dot1958
in
Vasculitis UK
Rituximab and puffy hands and feet
Puffy hands and feet after
rituximab
infusion, any one else had this?
Puffy hands and feet after
rituximab
infusion, any one else had this?
Susiebee31
in
NRAS
Rituximab?
Since ocrevus is not available in this part of the world, the next best drug recommended was
rituximab
. What is your opinion? I am hesitant , since a recent course (three injections) of steroids(solumedrol)did nothing to improve my condition.
Since ocrevus is not available in this part of the world, the next best drug recommended was
rituximab
. What is your opinion? I am hesitant , since a recent course (three injections) of steroids(solumedrol)did nothing to improve my condition.
canimambo
in
My MSAA Community
Cellular and humoral immune response to SARS-CoV-2 mRNA vaccines in patients treated with either Ibrutinib or Rituximab
The serological response was achieved in 0% of
Rituximab
treated, 18% of Ibrutinib treated and 50% of untreated CLL patients.
The serological response was achieved in 0% of
Rituximab
treated, 18% of Ibrutinib treated and 50% of untreated CLL patients.
gardening-girl
in
CLL Support
Rituximab covid paxlovid etc...
Last
rituximab
infusion was 6/22 (two total). Question: Should discontinuing methotrexate be considered at this point? It has been 2 weeks since the last dose. It did not reduce joint/muscle pain at all and was ineffective in reducing "bad levels" in labs after 7 months (these levels increased).
Last
rituximab
infusion was 6/22 (two total). Question: Should discontinuing methotrexate be considered at this point? It has been 2 weeks since the last dose. It did not reduce joint/muscle pain at all and was ineffective in reducing "bad levels" in labs after 7 months (these levels increased).
irishponies
in
Vasculitis UK
Rituxmab
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 tried on Imuran. I'm seronegative RA.
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 tried on Imuran. I'm seronegative RA.
Avi2013
in
NRAS
Rituximab Infusion
Anyone had
Rituximab
infusion? M having my first one on Monday as m worried and nervous Has it would for u ?
Anyone had
Rituximab
infusion? M having my first one on Monday as m worried and nervous Has it would for u ?
Mystik
in
Arthritis Action
Scleromytosis Rituximab
They have a high suspicion of myositis as well as scleroderma, they have recommended
rituximab
with reduced Mycophenelate. Anyone have any positive feedback about muscle aches/weakness, ILD and this medication combo. Always in need of hope x
They have a high suspicion of myositis as well as scleroderma, they have recommended
rituximab
with reduced Mycophenelate. Anyone have any positive feedback about muscle aches/weakness, ILD and this medication combo. Always in need of hope x
Aarts
in
Scleroderma & Raynaud's UK (SRUK)
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