Search
Search
About
Log in
Join
Experiences with
Rituximab
Posts
Communities
2,524 public posts
Filter results
Jak2 Inhibitors
Rituximab
for 18 months but it doesn’t really help and my R.a. D damage has deteriorated. I would really appreciate your comments. thank you.
Rituximab
for 18 months but it doesn’t really help and my R.a. D damage has deteriorated. I would really appreciate your comments. thank you.
debjw
in
NRAS
1 year ago
Advice on Rituximab
I hadn't been planning on getting another one but I feel like I should get one if I'm going to have the
Rituximab
. But if I don't end up having the
Rituximab
I won't get the next jab for now.
I hadn't been planning on getting another one but I feel like I should get one if I'm going to have the
Rituximab
. But if I don't end up having the
Rituximab
I won't get the next jab for now.
BookishVibes
in
LUPUS UK
1 year ago
Bronchocentric Glanulomatosis?
I'm just thinking that maybe the
rituximab
treatment might be the answer. I don't have faith in the medical support that she has been given so far and feel that she is being pushed from pillar to post. Any suggestions or information will be greatly appreciated.
I'm just thinking that maybe the
rituximab
treatment might be the answer. I don't have faith in the medical support that she has been given so far and feel that she is being pushed from pillar to post. Any suggestions or information will be greatly appreciated.
Muddywater100
in
Vasculitis UK
1 year ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
POST 5 - CAR-T cell therapy
Obviously the bridging treatment of five
Rituximab
infusions whilst continuing with Venetoclax had not cleared the bone marrow. The proposal is now to commence Acalabrutinib in the next few weeks to try and reduce the disease burden. IF it works I may still be able to join the Trial.
Obviously the bridging treatment of five
Rituximab
infusions whilst continuing with Venetoclax had not cleared the bone marrow. The proposal is now to commence Acalabrutinib in the next few weeks to try and reduce the disease burden. IF it works I may still be able to join the Trial.
casanova
in
CLL Support
11 months ago
PCNA gene attack -- for solid tumors
City of Hope’s groundbreaking translational research history includes developing the technology underlying synthetic human insulin and monoclonal antibodies, which are integral to widely used, lifesaving cancer drugs, such as trastuzumab,
rituximab
and cetuximab.
City of Hope’s groundbreaking translational research history includes developing the technology underlying synthetic human insulin and monoclonal antibodies, which are integral to widely used, lifesaving cancer drugs, such as trastuzumab,
rituximab
and cetuximab.
Derf4223
in
Advanced Prostate Cancer
10 months ago
Covid Booster - For Info
As far as the check of CEV was concerned I telephoned my consultants secretary last week as asked if I could have a copy of my latest report that detailed my last
Rituximab
infusion. I contacted my GP first because they have a copy of that letter from my consultant but they were totally unhelpful.
As far as the check of CEV was concerned I telephoned my consultants secretary last week as asked if I could have a copy of my latest report that detailed my last
Rituximab
infusion. I contacted my GP first because they have a copy of that letter from my consultant but they were totally unhelpful.
Investigator1
in
Vasculitis UK
1 year ago
Sjogrens and Eyes
On
Rituximab
Infusions. I was wondering if anyone has had little dots floating across their eye. ( just my right eye at the moment. ) I have the usual dry eyes and photosensitivity which has been very annoying of late. I find lights in shops very hard on eyes.
On
Rituximab
Infusions. I was wondering if anyone has had little dots floating across their eye. ( just my right eye at the moment. ) I have the usual dry eyes and photosensitivity which has been very annoying of late. I find lights in shops very hard on eyes.
Haired
in
Sjogren's Support
1 year ago
Stem cell transplant starts on Monday
Tests showed that I was resistant to the currently available BTKi's (two synergistic BTK mutations) and following the failure of the Bispecific T cell engaging antibody treatment to make any impression on my rapidly accelerating CLL I started Venetoclax and
Rituximab
in April 2022 as my 4th line of
Tests showed that I was resistant to the currently available BTKi's (two synergistic BTK mutations) and following the failure of the Bispecific T cell engaging antibody treatment to make any impression on my rapidly accelerating CLL I started Venetoclax and
Rituximab
in April 2022 as my 4th line of
Jm954
Administrator
in
CLL Support
11 months ago
RoActemera (tocilizumab) and headaches
I’d love to hear if the headaches abated with perseverance once body got used to them or perhaps if a change to
rituximab
worked. Thanks.
I’d love to hear if the headaches abated with perseverance once body got used to them or perhaps if a change to
rituximab
worked. Thanks.
momo17
in
Scleroderma & Raynaud's UK (SRUK)
1 year ago
Doctor mentioned Richters???
I am on the Bruin trial and was randomized to Arm B which is Idelalisib and
Rituximab
( 6 months of infusions ). My bloodwork so far has shown slight improvement since the start in January of this year.
I am on the Bruin trial and was randomized to Arm B which is Idelalisib and
Rituximab
( 6 months of infusions ). My bloodwork so far has shown slight improvement since the start in January of this year.
rcusher
in
CLL Support
1 year ago
Rituximab/ Covid
I took my
Rituximab
infusion last week and I’m worried about getting Covid in the future again Can anyone on
Rituximab
who caught Covid share their experience with me. Thanks
I took my
Rituximab
infusion last week and I’m worried about getting Covid in the future again Can anyone on
Rituximab
who caught Covid share their experience with me. Thanks
ks1966
in
NRAS
1 year ago
shall I go for the rituximab?
Hi all, I’m looking for people’s experiences with
rituximab
. I’ve had to come off tocilizumab after developing diverticular disease and I’ve been offered
rituximab
. I’ve heard scary things in the past about this so I was hoping to hear how people have found this drug. Many thanks 😊
Hi all, I’m looking for people’s experiences with
rituximab
. I’ve had to come off tocilizumab after developing diverticular disease and I’ve been offered
rituximab
. I’ve heard scary things in the past about this so I was hoping to hear how people have found this drug. Many thanks 😊
Springerfan
in
NRAS
1 year ago
Venetoclax for dummies
An example of an immunotherapy drug is
rituximab
, the "R" drug in FCR (the F drug in the combo is fludarabine, the C drug is cyclophosphamide).
Rituximab
binds to a protein on the surface of cancerous lymphocytes.
An example of an immunotherapy drug is
rituximab
, the "R" drug in FCR (the F drug in the combo is fludarabine, the C drug is cyclophosphamide).
Rituximab
binds to a protein on the surface of cancerous lymphocytes.
cajunjeff
in
CLL Support
11 months ago
rituximab nerves!
so, I have lupus and i'm due to have my first infusion of
rituximab
in the next month and I am extremely nervous- I'm not keen on this at all and not entirely sure it is necessary, i felt i was doing ok on the mycopehnolate but my dose has been upped and it gives me a terrible stomach- but i will obviously
so, I have lupus and i'm due to have my first infusion of
rituximab
in the next month and I am extremely nervous- I'm not keen on this at all and not entirely sure it is necessary, i felt i was doing ok on the mycopehnolate but my dose has been upped and it gives me a terrible stomach- but i will obviously
maeows
in
LUPUS UK
1 year ago
T-CELLs Collected
I am to resume taking Venetoclax, which was paused for the week prior to the T-Cell collection, and I am to have a weekly infusion of
Rituximab
during this period.
I am to resume taking Venetoclax, which was paused for the week prior to the T-Cell collection, and I am to have a weekly infusion of
Rituximab
during this period.
casanova
in
CLL Support
1 year ago
Rituximab
Can anyone tell me why
rituximab
treatments are restricted, I was told, to 2 years? I realise cost is involved, but I had my treatments in france, but was still refused it here in the uk. Back on Methotrexate now..
Can anyone tell me why
rituximab
treatments are restricted, I was told, to 2 years? I realise cost is involved, but I had my treatments in france, but was still refused it here in the uk. Back on Methotrexate now..
sarahdollygirl
in
Vasculitis UK
1 year ago
Rituximab
I'm scheduled for my first
Rituximab
infusion this week and getting cold feet ( second thoughts). Any advise and reassurance would be a great help Many thanks in advance. Kind Regards SfS
I'm scheduled for my first
Rituximab
infusion this week and getting cold feet ( second thoughts). Any advise and reassurance would be a great help Many thanks in advance. Kind Regards SfS
sorefeetsoldier
in
Vasculitis UK
1 year ago
Phase 1 trial testing CAR T-cell therapy GC012F in SLE
Common therapeutic approaches include the use of immunosuppressants, as well as medications that specifically target and destroy B-cells, such as
rituximab
.
Common therapeutic approaches include the use of immunosuppressants, as well as medications that specifically target and destroy B-cells, such as
rituximab
.
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
1 year ago
2 New Meds Found to Completely Change Lupus Nephritis Treatment
Spherix is speculating that reduced use of
rituximab
“may erode the bridge that most physicians see between
rituximab
” and Gazyva (obinutuzumab), an experimental treatment for lupus being developed by Roche. Gazyva has a similar mechanism of action to
rituximab
.
Spherix is speculating that reduced use of
rituximab
“may erode the bridge that most physicians see between
rituximab
” and Gazyva (obinutuzumab), an experimental treatment for lupus being developed by Roche. Gazyva has a similar mechanism of action to
rituximab
.
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
1 year ago
Tocilizumab for systemic sclerosis (with mild ILD) - any skin improvement?
Initially I was recommended to start
Rituximab
(both by rheumatologist and respiratory doctor) , now a few days ago I received a call from Dr. to tell me that the final decision is to start Tocilizumab.
Initially I was recommended to start
Rituximab
(both by rheumatologist and respiratory doctor) , now a few days ago I received a call from Dr. to tell me that the final decision is to start Tocilizumab.
FelixFelicis
in
Scleroderma & Raynaud's UK (SRUK)
1 year ago
1
...
8
9
10
...
100
Next page
10
20
30
40
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
CLL Support
1017 results
NRAS
566 results
Vasculitis UK
328 results
View top 10 communities
Sort by
Most Relevant
Newest