I started taking sulfasalazine a few weeks ago but am getting unpredictable bouts of tiredness, weakness and awful indigestion. Has anyone else experienced these side effects and any advice appreciated.
Sulfasalazine and Indigestion / Weakness: I started... - NRAS
Sulfasalazine and Indigestion / Weakness
Hi, I can’t remember if it was indigestion but I had to stop if due to nausea and occasional vomiting. Way too hard on the tummy…
Speak to your rheumatology team. If you don’t tell them they’ll assume everything is fine. They can give advice whether it’s likely to be the sulphasalazine causing it or something else. They can also advise whether to continue trying, reduce the dose or try something else.
I’ve taken sulphasalazine for 15 years and never had any problems with it at all (despite having horrible side effects to other things) but a friend of mine ended up in hospital for several days due to side effects from sulphasalazine. We are all different so seeking medical advice is the sensible thing to do. If you have a nurse helpline call them. If not phone the main hospital number and ask for either your consultants secretaries phone number or email address.
Make sure they are ‘coated’. As above, write down any side effects & inform your Rheumatologist.
thank you for your reply - they are the coated ones but I will let the rheumatology nurse know.
Ask for omeprazole to help your stomach 🏋🏻♂️
thank you I will press ahead and ask for that.
it has helped me for five years👨🔬👩🔬
that is good to hear - did the omeprazole give you any side effects
Sulfasalazine gave me terrible acid heartburn. Ask either your rhuemy or GP if you have access to one for lansoprazole or similar. It worked wonders for me. The tablets reduce the amount of acid in your stomach. I felt dizzy and naff too when I started taking them, but it wore off as my body for used to them. I took Sulfasalazine for years and it got me into remission for some time. Good luck.
hi ! I took sulfasalazine for 6 weeks ( alongside 5mgs of Pred ) and had to stop taking it as it left me feeling nauseous all the time ☹️ I’m now on leflunamide and so far 2 weeks in and no sickness 🤞🤞🤞 Had a blood test this morning so also hoping my ALT levels are ok ( methotrexate sent it rocketing from 12 to 327 😩 ! ) we all react differently but this this helps x
Sulphasalazine increasingly made me very fatigued with heartburn and a wheeze everytime I increased the dose as instructed by rheumatology.
I asked my GP for advice about the increasing wheeze, and how unwell I was feeling, he told me to increase my sulphasalazine. (This was in the early days of my RA experience).
But, knowing the wheeze and sulphasalazine dosage were related I contacted rheumatology who told me not to take any more until seen.
I was given an emergency appointment next day, was seen by my rheumatologist who examined me, listened to my wheeze, diagnosed a salicylic acid allergy and discontinued it immediately.
Lessons learned, always contact rheumatology for advice on the meds they prescribe.
(I'm fine eating foods with salicylic acid in them, it was the high dose in sulphasalazine that was the problem. Although I did get strawberry rashes as a child, when I gorged myself on them).
Hello there yeah all of the above I had to come off it, well I then went onto Methotrexate. I really really would talk to your Team really didn't agree with me. Really hope that helps you. Take care.
Welcome take care 🙂