Bad experiances with humira? | Arthritis Information

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Hi,
I am new to this site. I was diagnosed with RA in 2000. I have not had much luck with any meds. I have aleady had two joints replaced. anyway, I am now on Humira. It doesn't seem to be working for me. my joints are still being destroyed. Everything I read about it makes it sound like a wonder drug. anybody have any experiences with it??

Linda--

How long have you been on it?  Are you taking anything else with it?  Have you given it enough time to do its thing?

Hi Sara,
I have been on the Humira since April, right after my hip replacement surgery. I also take celebrex. I do seem to feel better, less stiffness and not as tired all the time but it seems as if my joints are still being destroyed. my surgeon thinks my other hip is already bad and it never hurt before i started the Humira. nothing else really worked for me, so I guess I just don't have a lot of confidence in it.

Will, I don't take Humira.  I use one of the other biologics, Kineret.  But from this board, I get the idea that it takes a few months to really kick in.  You might need to give it a bit more time.  Not sure.  Also, Lots of people here take methotrexate along with Humira.  In fact, the FDA suggests that it be taken in conjunction.  Here's a website that might be of interest to you regarding the biologics.  Something for you and your rheumatologist to discuss...

http://www.rheumatology.org/public/factsheets/biologics.asp? aud=pat

Take care.

Everything I've read says it takes a while for the Biologics to kick in. Most of us who are on a biologic are also taking MTX as well, and still may need a pain reliever, as well as folic acid.

When I was on Enbrel it took about 6 weeks to have any effect at all. And it never really worked well, so I "failed" Enbrel.  I switched to Humira and it began working a little sooner, after the 3rd shot..

They doubled my MTX dose, and now I am having more reliable response from the Humira.

thanks for the info, guys. I guess I just have to be patient. I do have a new dr. and I see him next week so maybe I will discuss the mtx with him. I have never had the experience to talk to other people with RA, so this is a lot of good info for me.
thanks,
Linda
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