Sulfasalazine: Hi. My Rheumy has just prescribed me... - LUPUS UK

LUPUS UK

32,145 members28,486 posts

Sulfasalazine

Megan2005 profile image
3 Replies

Hi. My Rheumy has just prescribed me Sulfasalazine to take along with Leflunomide (been on this for 3 years). Anyone out there had any side affects with  Sulfasalazine? 

Written by
Megan2005 profile image
Megan2005
To view profiles and participate in discussions please or .
Read more about...
3 Replies
creaky profile image
creaky

Sulfasalazine was the first drug I was prescribed for my joints, I took it for 5 years, at first it worked really well, relieved all my morning symptoms. 

Don't remember suffering any side effects other than producing the alarmingly orange urine, which actually would stain the loo! 

Lots of bleach needed.

Sorry to be graffic but you did ask☺

Hope it does to trick for you. 🍀 

ripecherries profile image
ripecherries

the only side effects I got was yellow skin and bad hair loss, also made me feel sick but sulfasalazine did help with the R A.

Silvergilt profile image
Silvergilt

The staining of the urine was the only big one I can remember. This medication for me personally was brilliant, I almost felt like my old self again, even started lifting weights. However, what they didn't tell me was sulfasalazine has a very short shelf life of effectiveness; only two to three years. It's a temporary solution, so if it helps, enjoy it!

Not what you're looking for?

You may also like...

sulfasalazine

Hi My rheumatologist wants to change my medication from hydrochloroquine to sulfasalazine. Is...

Sulfasalazine medication for RA and lupus

I have lupus and RA. I was on Methotrexate and Meloxicam but due to side effects and high blood...

Lupus and COVID-19 Vaccination - UPDATED 03/09/2021 - Third Doses

Following new JCVI recommendations announced earlier this week, we have updated our information and...

Methotrixate, ciclosporin, cyclophosphamide, or sulfasalazine????

Can anyone help with the above medications? Im reluctant to go on methotrixate cos I like my...

Azothiaprine and recurrent neutropenia MCTD

Hi all, I was diagnosed with MCTD this Feb. I have severe raynauds, pain and swelling in all of my...