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Rituxan
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Rituxan infusion day 2
My experience with my
Rituxan
infusion is that i was very scared to get this infusion after reading all the side effects but now I'm in day two after nit sleeping for 35 hours and woke up in a lot of pain the yesterday was nice having no pain after all the steriods they give you before the infusion.
My experience with my
Rituxan
infusion is that i was very scared to get this infusion after reading all the side effects but now I'm in day two after nit sleeping for 35 hours and woke up in a lot of pain the yesterday was nice having no pain after all the steriods they give you before the infusion.
Shresworld
in
NRAS
3 years ago
Rituxan
My skin issues keep getting worse and my Oncologist has just recommended a 4 week (once per week) infusion of
Rituxan
. Does anyone have experience with this? Thankful this is a minor issue. Thank you!
My skin issues keep getting worse and my Oncologist has just recommended a 4 week (once per week) infusion of
Rituxan
. Does anyone have experience with this? Thankful this is a minor issue. Thank you!
mkuhlman
in
CLL Support
3 years ago
Digestive symptoms with high atypical anca
I have MPA and been in remission for 6 years with no
Rituxan
since 11/2019. Rheumatologists and I are comfortable with monitoring labs every 3 months and holding off on any treatment until labs/symptoms indicate the need.
I have MPA and been in remission for 6 years with no
Rituxan
since 11/2019. Rheumatologists and I are comfortable with monitoring labs every 3 months and holding off on any treatment until labs/symptoms indicate the need.
Sybennett
in
Vasculitis UK
3 years ago
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Vaccine & flare
Just finally getting back under control with increased Revlimid & Imuran ( along with
Rituxan
infusions)
Just finally getting back under control with increased Revlimid & Imuran ( along with
Rituxan
infusions)
Expectthebest
in
Behçet's UK
3 years ago
Bendamustine & Rituxan Remission?
How long did Bendamustine &
Rituxan
keep you in remission?
How long did Bendamustine &
Rituxan
keep you in remission?
LlHoot
in
CLL Support
3 years ago
Side Effects of Bendamustine?
They start
Rituxan
and Bendamustine next week. With all the treatment I have had, I have never had this one, so I am wondering if you could share what your experiences were. Thanks much.
They start
Rituxan
and Bendamustine next week. With all the treatment I have had, I have never had this one, so I am wondering if you could share what your experiences were. Thanks much.
KevinCLLITP
in
CLL Support
3 years ago
Followup to my post 8 months back, sudden jaundice and hemolytic anemia
Couple of questions I have is can we start him on IVIG immediately to get his platelets up temporarily until his other meds (eltrombopag,
rituxan
) start kicking in or wait as he still stable right now with no bleeding incidents. Thanks!
Couple of questions I have is can we start him on IVIG immediately to get his platelets up temporarily until his other meds (eltrombopag,
rituxan
) start kicking in or wait as he still stable right now with no bleeding incidents. Thanks!
Akam
in
Hughes Syndrome APS Forum
3 years ago
Muscle pain after MPA remission
Thankfully
Rituxan
put into remission and have been disease free since. Does anyone else who is remission still experience muscle pain disproportionate to the level of exertion? Did a set of 8 body weight squats this week and my quadriceps are unbelievably sore.
Thankfully
Rituxan
put into remission and have been disease free since. Does anyone else who is remission still experience muscle pain disproportionate to the level of exertion? Did a set of 8 body weight squats this week and my quadriceps are unbelievably sore.
Sybennett
in
Vasculitis UK
3 years ago
chemo tomorrow
Starting Bendamustine
Rituxan
tomorrow, six treatments, probably maintenance after. I am 73 in good health, stage 3, type 3a. no bone marrow or organ involvement, largest node 3 cm. mostly smaller, located neck, upper abdomen, groin, etc. minimal symptoms. Chose chemo over watching.
Starting Bendamustine
Rituxan
tomorrow, six treatments, probably maintenance after. I am 73 in good health, stage 3, type 3a. no bone marrow or organ involvement, largest node 3 cm. mostly smaller, located neck, upper abdomen, groin, etc. minimal symptoms. Chose chemo over watching.
newerguy
in
Non Hodgkin's Lymphoma Friends
3 years ago
The CDC FINALLY talks about the problem of immunity in the immunocompromised. People on Ocrevus, Rituxan, Kesimpta and similar..take note.
If you are on DMT’s like Ocrevus,
Rituxan
and Kesimpta, please talk with your medical team and don’t assume that fully vaccinated gives you immunity. https://www.cnn.com/2021/07/16/health/cdc-warning-covid-19-vaccine-immunocompromised/index.html
If you are on DMT’s like Ocrevus,
Rituxan
and Kesimpta, please talk with your medical team and don’t assume that fully vaccinated gives you immunity. https://www.cnn.com/2021/07/16/health/cdc-warning-covid-19-vaccine-immunocompromised/index.html
Raingrrl
in
My MSAA Community
3 years ago
Treatment advised (after 21 years w & w)
I was also given a leaflet on
Rituxan
but I am not sure how this would fit in (could it be combined with Venetoclax as a first-line treatment in the UK?)
I was also given a leaflet on
Rituxan
but I am not sure how this would fit in (could it be combined with Venetoclax as a first-line treatment in the UK?)
ornstin
in
CLL Support
3 years ago
Relapsing on Ibrutinib
One is Venetoclax and
Rituxan
, the alternative is a clinical trial with MK1026. Had anyone heard about this new drug (BTK inhibitor), by any chance? I have faith in you!
One is Venetoclax and
Rituxan
, the alternative is a clinical trial with MK1026. Had anyone heard about this new drug (BTK inhibitor), by any chance? I have faith in you!
Doremefasol
in
CLL Support
3 years ago
I have had both doses of the Pfizer vaccine, while they applauded me after I got my 2nd dose, 90 days later I found that I have no immunity!
It would seem that
Rituxan
is the main culprit, as in my research I found that no immunity was created in cases which had received
Rituxan
within a year. Although a bit more, Ibrutinib is around 14-15% and Venetoclax is 19-20% of cases established immunity.
It would seem that
Rituxan
is the main culprit, as in my research I found that no immunity was created in cases which had received
Rituxan
within a year. Although a bit more, Ibrutinib is around 14-15% and Venetoclax is 19-20% of cases established immunity.
KevinCLLITP
in
CLL Support
3 years ago
Experiences with Rituxan,Bendeka,and Neulasta
On a regimen of
Rituxan
and Bendeka and Neulasta for 4 months dealing with marginal zone lymphoma that morphed into follicular lymphoma. Experiencing shortness of breath and extremes of fatigue. Anyone out there with their personal experiences with this protocol. Thank you for any info, Lee
On a regimen of
Rituxan
and Bendeka and Neulasta for 4 months dealing with marginal zone lymphoma that morphed into follicular lymphoma. Experiencing shortness of breath and extremes of fatigue. Anyone out there with their personal experiences with this protocol. Thank you for any info, Lee
Whalexx
in
Lymphoma Canada
3 years ago
Anyone with these neurological issues and health complications?
The rheumatologist has me on CellCept and
Rituxan
, and will be adding Actemra next week. My question is this, has anyone else experience similar rapidly progressing neuromuscular/neurological symptoms in a similar context? If so, what was the outcome?
The rheumatologist has me on CellCept and
Rituxan
, and will be adding Actemra next week. My question is this, has anyone else experience similar rapidly progressing neuromuscular/neurological symptoms in a similar context? If so, what was the outcome?
TiredNerd
in
NRAS
3 years ago
Doctor wants to start Venetoclax today but recent blood work shows evidence of AIHA but Doctor still says start Ven
I think the
Rituxan
will put him in control of not only the anemia but also the CLL
I think the
Rituxan
will put him in control of not only the anemia but also the CLL
Palmetto
in
CLL Support
3 years ago
Socializing while on Rituxan and Cellcept
I would like to hear about your experience regarding your socializing with others while on
Rituxan
and Cellcept. I know these drugs will reduce your immune system and need to be careful about being around people.
I would like to hear about your experience regarding your socializing with others while on
Rituxan
and Cellcept. I know these drugs will reduce your immune system and need to be careful about being around people.
NebraskaTexas
in
Encephalitis Society
3 years ago
Important SARS-CoV-2 and Covid-19 information for Chronic Lymphocytic Leukaemia/CLL patients
In addition, they may experience: • Treatment-related immunodeficiency (such as that resulting from anti-CD20 monoclonal antibody treatment such as Rituximab (Mabthera/
Rituxan
), Obinutuzumab (Gazyva) or ofatumumab (Arzerra) In a recent study, ‘individual risk factors associated with a poor prognosis
In addition, they may experience: • Treatment-related immunodeficiency (such as that resulting from anti-CD20 monoclonal antibody treatment such as Rituximab (Mabthera/
Rituxan
), Obinutuzumab (Gazyva) or ofatumumab (Arzerra) In a recent study, ‘individual risk factors associated with a poor prognosis
CLLerinOz
Administrator
in
CLL Support
2 years ago
Tophaceous Gout and CLL Drugs
The past two years I have been on Ibrutinib, and two of its derivatives, then nothing for about six months at which time I had a serious case of hemolytic anemia after which I was put on Venclexta and 6 rounds of
Rituxan
.
The past two years I have been on Ibrutinib, and two of its derivatives, then nothing for about six months at which time I had a serious case of hemolytic anemia after which I was put on Venclexta and 6 rounds of
Rituxan
.
KevinCLLITP
in
CLL Support
3 years ago
Second chemo round
For my first chemo I did
Rituxan
and Bendeka and was in remission for 2 1/2 years. My last appointment my doc told me it is time to go back on chemo and mentioned oral chemo. I am in the process of getting a lot of testing done before I go back to the doctor.
For my first chemo I did
Rituxan
and Bendeka and was in remission for 2 1/2 years. My last appointment my doc told me it is time to go back on chemo and mentioned oral chemo. I am in the process of getting a lot of testing done before I go back to the doctor.
J-girl
in
CLL Support
3 years ago
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