Hello all, I've been having a very bad flare for a while. I already take hydroxychloroquine and methotrexate injections. My consultant has suggested methylprednisolone iv. Does anyone have any experience or advice as I don't know much about what to expect. Thank you
methylprednisolone iv: Hello all, I've been having... - LUPUS UK
methylprednisolone iv
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Yes. I had two emergency doses 4 days apart 8 years ago. I puffed up alot initially but it controlled my flare. It was worth it.
I had some of this years ago - three 250mg doses Methylpred on consecutive days. Was fairly unpleasant, but I was so ill I didn't care. My kidneys were in freewill - and the steroid was an attempt to arrest that. Still here to tell the tale.
Hi I take Sulphasalazine, Methotrexate and Hydroxychloriquine. I have had a few flare ups and have had a Steroid injection in my upper buttocks a few time. Can't have these very often and should be at least 6 months apart to avoid any side effects! I find these amazing and feel normal within a few days. Definitely worth a try to get you back on track. I don't take Steroid tablets or injections into joints. Kenalog is the injection I have on occasion for flare ups. I have Sero negative RA. Hope this is helpful! Good luck and feel better soon! P.s. injections not sore just a prick !