I have just received a copy of the letter that my RA consultant has sent to my GP. I'm being started on early aggressive therapy and I will be commencing on Hydroxy chloroquine and Sulfasalazine. Has anyone had any experience of these drugs? Are they tablet form or injected, do they have bad side effects, if so do they subside once your body gets use to it?
I have just Googled these drugs, and there doesn't seem to be any alarming side effects, also they are administered orally, I am still interested in anyone's experience of these drugs.