PsA and Otezla: Just about to start a fairly no drug... - NRAS

NRAS

36,567 members45,171 posts

PsA and Otezla

Scottiedottie profile image
7 Replies

Just about to start a fairly no drug called Otezla. Have had 2 DMARDS without success. Anyone else on this? The beauty is no blood tests every fortnight! My veins will be pleased

Written by
Scottiedottie profile image
Scottiedottie
To view profiles and participate in discussions please or .
Read more about...
7 Replies
AuroraB profile image
AuroraB

Yes, been on it for over a year now. Had a lot of diarrhoea and some nausea when I started but that settled after about 3 months. Has impacted a little on tendonitis - like all these drugs variable responses with different folk so hoping you see a good effect and are not troubled too much by any side effects. Good luck.

Scottiedottie profile image
Scottiedottie in reply to AuroraB

Thanks.

oldtimer profile image
oldtimer

I had to look it up: psoriasis.org/about-psorias...

sounds as if this is more for the psoriasis skin problems than the arthritis?

Scottiedottie profile image
Scottiedottie in reply to oldtimer

Not necessarily. It's been approved for both especially where there is active dactylitis. Aka Sausage fingers

flow4 profile image
flow4

How are you getting on with it, Scottiedottie? I had to come off it because it gave me unbearable migraines, which was sad, because it did seem to help.

Scottiedottie profile image
Scottiedottie in reply to flow4

Came off after 6 weeks. Nausea and f2f uarrhoea. Sinus infection know on Hydroxychloroquine. No effect yet. Thanks for asking

flow4 profile image
flow4 in reply to Scottiedottie

It's such a nuisance, isn't it? Hydroxy caused a big psoriasis flare for me. I'm back just on mtx and NSAIDs now, plus dietary changes, and doing ok. Hope you find the combination that works for you.

You may also like...

Was PsA now undifferentiated!

I've had everything from 'it's all in your head' to maybe vasculitis, RA, blah blah blah...and then...

RA, PSA, lupus or what?!

biologics if the team think it's worthwhile. Has anyone else had this and what happened?

Toenails and PsA (there is a photo)

thought. My finger nails all have very faint vertical lines with sparse but fairly regular splinter...

Sneakers/shoes for PsA, orthotics and toe/feet pain?

I have extreme foot pain after walking for about thirty minutes or more. I think most of the pain...

Conflicts with dermatologist vs rheumatologist. PsA and methotrexate

doctor. Maybe I should get another dermatologist! Anyone had this problem?