Anyone on Simponi?
I have tried Meth, was taken off that because my gums were swollen, bleeding and with the other side effects my Rheumy said I'm allergic to it. So we went to Humira. Been on that for several months and then noticed that everytime I give my injection I would break out with hives in my abdomen. So, again, I was told to get off it because I am showing signs of being allergic. I am supposed to start Simponi next week and wanted to know if anyone else is on it and their experience. I've not heard anything about it so I'm just curious.
It's a pretty new drug, so I haven't seen a lot of information on it from the point of view people living with RA. I have seen a number of questions asking about it, so it looks as if more doctors are prescribing it. Try asking your question again in the SharePost - they sometimes get more traffic than the Q&A section.
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I am on Simponi now and am having good results. The shot is so much less painful than Humira.
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