Has any experienced increased join pain of sulfasalazine?
Posted , 6 users are following.
I'm on 3 rd wk 3 500mg daily - the headaches & being tired is already miserable. Yet the increased pain in my joints is unbearable actually feels like a full on flare - my hips ,wrists & feet are aching more then ever . Even with increased pain meds I am getting no relief I feel 100times worse with the meds then I did without them . Also taking 5mg prednisone which dose seem to make a difference since increased dose to 3 Sulfasalazine. Any one else experienced this?? I have RA & PSA
0 likes, 5 replies
treezsh kelly33023
Posted
Yes, sorry to hear this but i too had many problems with Sulphasalazine, headaches and continued joint pain ++ biologics were the only things that worked for me in the end. Good luck
EileenH kelly33023
Edited
Aching joints is a symptom that the Mayo site says should be notified to your doctor immediately:
https://www.mayoclinic.org/drugs-supplements/sulfasalazine-oral-route/side-effects/drg-20066179
Jayjay1959 kelly33023
Posted
Hi Kelly
I too was like you 10x worse I was allergic to the ingredients pain worse, fidgeting unable to keep still constantly shooting pain in all joints and joints on fire
came off it after a brief time
went onto biological after that don't suffer in silence tell your RA team immediately
good
amkoffee kelly33023
Posted
What is PSA
EileenH amkoffee
Posted
In this context I assumed it was psoriatic arthritis