I was wondering if anyone has experience of Rituximab; I think it's called something else in USA.
I have written about my wife's trials and tribulations with RA medications, she recently failed on Tocilizumab trials, has had pretty much every anti TNF drug and has now been advised to start Rituximab.
Any experiences on this drug IE: success, fail, ill, side effects?
I have read the official blurb but looking for personal experience.
Thanks in advance.
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