Thoughts On Rituxan
I'm starting Rituxan in a couple of weeks (previously on Actimera and cellcept, which was hurting my liver levels, AST and ALT). What are others experience with Rituxan successes, and side effects?
I've been on Rutuxion for a few years once every 6 months. It's working for me so far. I am happy for the financial assistance as well.
I've been on Rituxan for about 5 years, twice every 4 months. I've had no issues.
Thank you everyone! So far my first dose hasn't been too promising, but I'm not giving up. I'm not having much inflammation but numbness and tingling is still a big problem. Next infusion in June.
Actually this is a question, I have never heard of this Rituxan does anyone know if there is something that helps with this constant tiredness? And does that Rituxan help with that I am now on Rinvoq it has helped keep more crippling at bay but I am getting the weakness in my wrist's . I have been on the other meds that have Been mentioned. Usually what ever I am taking only works for about a year and a half. Is anyone else going through that. And thanks for any input.😘
I just started Rituxan in December after no luck with a number of different drugs.
So far so good. I know it’s early days but I do feel as if my hands are better and my overall pain has decreased. I have a follow up appointment with my rheumatologist. The end of April and the next Rituxan infusions are booked in June. I too am thankful for the co-pay because otherwise, there is no way I could be taking this drug.
After a lot of fails, I am hoping that this biologic is going to be a game changer for me. Good luck to you.
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