Rinvoq and spondylitis | MySpondylitisTeam

Connect with others who understand.

sign up Log in
Resources
About MySpondylitisTeam
Powered By
Real members of MySpondylitisTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.

Top 10 Search Results for "Rinvoq"

reset
Has Anyone Experience With RINVOQ? How Does It Work For You?
A MySpondylitisTeam Member asked a question 💭
•
View reactions
A MySpondylitisTeam Member

I take Rinvoq and so far have had good luck at least on the Psoriasis side. I'm unfortunately beginning to accept there just isn't a help for the pain.

I Have Had AS 33 Years. Just Started Rinvoq. Wondering If It Has Helped Anyone And If They Had Any Reactions To It. Thank You.
A MySpondylitisTeam Member asked a question 💭
A MySpondylitisTeam Member

I take sulfasalazine and rinvoq. No bad experiences with the med. Sometimes I start thinking the meds don5 help a lot, as the pain still is with me, but I sure do notice a huge spike in pain without… read more

Anyone Try Rinvoq For AS?
A MySpondylitisTeam Member asked a question 💭

I have had good results except fatigue is on another level!

•
View reactions
A MySpondylitisTeam Member

Rinvoq is a JAK inhibitor. For me personally I found the risk factors were too great.

What Class Of Drug Is Rinvoq?
A MySpondylitisTeam Member asked a question 💭
3 Types of Self-Injections for Spondylitis: Pros and Cons Read Article...
A MySpondylitisTeam Member

Thanks Marloes!😷

Is It Recommended To Have Surgery With Spontaneitis?
A MySpondylitisTeam Member asked a question 💭
•
View reactions
A MySpondylitisTeam Member

Anyone have experience with Rinvoq? I was on Humira for 12 years, the efficacy decline greatly leading to 2x month and a lot of skin cancer. Switched to Taltz, in 18 months I was bedridden with very… read more

Has Anyone Tried Rinvoq?
A MySpondylitisTeam Member asked a question 💭

My doctor decided to switch me due to humira injection site reactions and becoming less and less effective with every injection. I know rinvoq is new. Just wondering what kind of experience people are having with it. Thank you

•
View reactions
A MySpondylitisTeam Member

I'm about to start Rinvoq after humira losing its potency for me. Should get it tomorrow, hopefully it's working out for you!

What Is Another Medication For Ankylosing Spondylitis. Currently On Humira. In So Much Pain Still
A MySpondylitisTeam Member asked a question 💭
Weather and Spondylitis Symptoms Read Article...
A MySpondylitisTeam Member

Rinvoq not working for me anymore either. Consentx and Humira worked pretty good. Briefly was on Methylprednisilone for 7 days and it took almost all symptoms away but you can only take it briefly… read more

Rinvoq - JAK1 Inhibitor??
A MySpondylitisTeam Member asked a question 💭

Anyone have experience with Rinvoq? I was on Humira for 12 years, the efficacy decline greatly leading to 2x month and a lot of skin cancer. Switched to Taltz, in 18 months I was bedridden with very serious IBD. Currently taking prednisone daily.

At 71 it is being suggested I try Rinvoq. There are a lot of bad side effects and I am trying to weigh quality of life with the risks including blood clots, infections, heart attack, stroke, cancer, stroke, etc. Overall health is pretty good but I… read more

•
View reactions
A MySpondylitisTeam Member

Tiger balm

Switching From Enbrel
A MySpondylitisTeam Member asked a question 💭

Hi, I've been on Enbrel for over 15 years and can feel it's not working so great any more. Has anyone here switched from Enbrel to new treatment which worked well? Enbrel is one of the best ones and I'm worried not much else will work that well. Thank you

A MySpondylitisTeam Member

Rinvoq works pretty well for me! Good Luck!🥰

I Am On Rinvoq And It Isn't Working. Has Anyone Tried Other Meds To Help? I Especially Have Fatigue Which I Am So Sick Of.
A MySpondylitisTeam Member asked a question 💭
•
View reactions
A MySpondylitisTeam Member

Yes, be frank with your doctor and tell them what symptoms you are still having and the intensity of them your medication‘s can be adjusted or changed to find one that works better for you