Experiences with

Rituxan

Three cheers for 6 doses of Rituxan and 24 months of Venclexta!! I have achieved MRD!!!

Now doctor wants me to take Rituxan and taper off prednisone. Looked up side effects even though the doc said not to do that as it was very safe. 🤬 Looking for any advice from anyone with experience with Rituxan and also with coping this disease that I had never heard of.

It's Rituxan time 😴 nothing like relaxing in a recliner not having to do anything while amazing nurses take care of you ❤️

I’m on Venetoclax and Rituxan for NHL. I need to go to the dentist. I think it’s a cavity but my luck, a root canal. What is a good antibiotic to take that does not interact with Venetoclax? I’m not getting any answers from my oncologist.

Finished up six months of Rituxan-Bendamustine for follicular NHL, PET scan at halfway point was clear, have another PET in a week for final results. Anyone use Rituxan maintenance every other month for two years?

Treatment Rituxan and steroid Infusions. Every 6 months to a year of remission. I High dose Cannabis. The cancer protocol. It helps with disease. I want to know about your pain? I know CRP. All the markers. Is anyone in as much pain, but different from Rituxan? Intense pain.

Did anybody not get there 2nd Rituxan infusion the one that you get 2 weeks later due to side effects. If so did one help at all ?

With the latest cocktail of meds, (prednisone, mycophenolate and Rituxan) his doctor thought the encephalitis would show improvement or be totally gone by now. His doctor is talking about taking him off mycophenolate and Rituxan and add infusions of Cytoxan.

Has anyone taking Rituxan and or Prednisone have any problems with their hair? Like hair falling out or being coarse?

Like many of you, I'm immunocompromised from years of prednisone, azathioprine and Rituxan. Two years ago today, April 3rd, 2020, in spite of sheltering, I wound up in the hospital with COVID-19. Not as much was known about COVID then and there were no vaccines yet.

Did anyone have problems with their kidneys and Rituxan infusion?

Has anybody had kidney pain or problems with your kidney after a Rituxan infusion?

Rituxan side effects remission

My husband 69 years old is on Calquence for CLL, he's had Chemo at least three times over about 15 years, Bad reactions to Rituxan, weird skin issues, looked like tick bullseye rings that started on the upper torso traveled down his body, down his arms and legs and then disappeared, he was in remission

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!

Does anyone take rituxan and hydroxychloroquine? I can't find any information on it. Its seams it would help for viruses just wondering if it would be a good combo.

I am due to soon start Rituxan. All very new and a very interesting side effect of disease is tingling feet!! They throw me off my balance!! I have been trying compression socks and they help with balance.

Ok its been 1 week today since my first Rituxan infusion and 2 days ago I started get a pain in my left side of my back now stomach pain. I have read that those are some of the side effects just wondering how many have experienced side effects and for how long?

My doctor only intervenes with a medicine (IVIG, Rituxan, etc) if I am having bad symptoms (bleeding or petechiae). Since I tell him when I am experiencing those symptoms I don't feel the need to check the numbers so frequently.

Thank god he did very well on his initial treatment of Prednisone and Rituxan. That lasted 4 weeks, then we moved on to the oral med of CALQUENCE, which is how I found this site. My husband after 1 week experienced severe headaches. Not sleeping, not able to each, nauseous.