Does anyone use or have knowledge of sulfasalazine taken together with a biologic? My RA doc, pharmacist and i are looking at my taking sulfa with Cimzia. Sulfa on its own has worked best for me, while methotrexate has had no effect. Any help is greatly appreciated!
Sulfasalazine used with a biologic?: Does anyone use or... - NRAS
Sulfasalazine used with a biologic?
Humira, hydroxy, methotraxate and sulpasalazine all last year.
Taken off the hydroxy this year and Imraldi instead of Humira but still on rest of it.
Still get swelling, tiredness and soreness quite often but mostly improved and attending full time work 90% of the time.
Listen to your medical team....what works for others may not work for you.
Totally agree with, work with the medical team
Yes I take sulphasalazine (4 a day) with a biologic. It seems methotrexate is the more common one, but it doesn't suit everybody.
Yes I take sulpha with Abatacept( Orencia) . Can't tolerate methotrexate. Mostly well controlled at the moment.
Have been on methotrexate for 3 years doing ok with intermittent flares until Christmas out of control since. Due to start sulfascazine and etanercept along side methotrexate in September 🤞
I took Sulpha with Simponi (Gulimumab) for just over 3.5 years but have just been switched to Humira and am continuing (at least for now) with Sulpha with it. Had to wait 9 weeks for the switch which became a nightmare but after 1st injection last Sunday things improved for several days but not so good now. Hoping after 2nd injection next Sunday it will start improving again. Simponi just stopped working properly, although perhaps not entirely since it was only about 6 weeks after last injection that things got much much worse so it was working a little just not enough to do any good in the last months of use.
I take Sulfasalazine with Benepali
It works for me
Brian
Sulfasalazine prednisolone hydroxychloroquine pregabalin and Abatacept.Tried 3 other biologics and Abatacept best
Yes, me!I have sulfasalazine, mtx and Cimzia.
And how is it working for you, Moomin8?
Morning 🙂Seems to be ok 🤪I am able to lead a 'normal' life: I work, walk, drive, garden, see friends and holiday etc. My hips slow me down somewhat, but I take paracetamol and anti-inflammatories to keep the edge off that pain. I try to exercise every morning to stretch my limbs and keep as supple as I can. Sometimes my bloods dictate that my mtx is reduced because my neutrophils dip too low...but hey ho- I am generally not too bad.
At one time it was MTX, Sulfasalazine and CIMZIA together. No problems at all. I hope you won't have any either. Good luck.
Yes, like others I've been on sulfasalazine since 2002, other drugs have come and gone but that & Prednisolone have stayed the same. Was on Enbrel now on Imraldi via Leflunomide, Rituximab and Humira. This is a completely individual condition and you and you RA team need to decide what is best for you. Wishing you all the very best and that you find the right combination for you
I have taking Sulfasalazine for years along with a biologic, at present time I am on Orencia infusions, but I have taken Cimzia injections in the past too. When I first started Sulfasalazine it caused headaches, but they were tolerable and did not last long ,other than that I haven't had any side effects. My daughter could not take it because her headaches were severe while on it. I hope it helps bring you relief.
I am currently on Benepali and Methotrexate, Hydroxychloroquine and Sulfasalazine, though I’m reducing Sulfasalazine very slowly. Last reduction from 2 to 1 tablet a day not gone well as my hands and knees are swelling a bit and are quite painful again. I’m waiting to make sure it’s not a flare (I know I’ve been doing too much!) and also to get latest blood results before I call the nurse for advice. Hope it goes well for you.