Sulfasalazine and depression: I've seen a few older... - NRAS

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Sulfasalazine and depression

Pollymolly profile image
17 Replies

I've seen a few older posts on this ... but wondering if anyone has any experience or knowledge about sulfasalazine and depression?

I have a history of depression / anxiety, but it's usually controlled okay. But I've been really struggling the last couple of months, with pretty intense paranoia and thoughts about dying. I saw the RA nurse this week and didn't want to admit how bad I've been feeling. I just said I'd had a low mood for the past few months, she was checking to see if hydroxychloroquine had any emotional effects as she didn't think it did but she knew sulfasalazine did.

But I wasn't depressed like I am now when I started hydroxychloroquine last year. It made me realise things have only got really bad since I started sulfasalazine. I've also really struggled with cognitive things. she said she'd see me in 6 weeks rather than 12, but if sulfasalazine is causing this I just want to stop it now. I can't keep having to work so hard to rationalise staying alive!

I've not noticed any improvements in pain/stiffness, but I understand it can take a while.

I don't understand the pharmacology of it though, how an RA drug can affect mood ...

Anyway, interested to know if anyone else has had psychological effects from this med.

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Pollymolly profile image
Pollymolly
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17 Replies

Hello Polly. When I went on Sulfa my doctor asked me if I ever suffered from depression. I told him I have never suffered from depression. I understand it is a rare side effect.

I am on hydroxy and sulfa. For the first few weeks on Hydroxy I was having violent dreams. They have subsided now.

I think you should notify your doctor that you are getting depressed. You shouldn't have to suffer emotionally. There are other drugs out there. Pleases don't suffer.

Take care

Sue

Ruth273 profile image
Ruth273

Hi Polly,

I would definitely speak to your GP, Nurse or RD nurse sooner rather than later; they can help with this. It is not worth feeling bad when things may improve just by something as simple as changing your medication.

Please don't change anything with your medication until you have spoken to them though as there may be other factors involved and they are the best to advise on this. One of the side effects of Sulfasalazine can be depression so it is worth asking them if this could be a factor in why you feel as you do.

I know when I was on Sulfasalazine I was very depressed and paranoid and was taken off it for this reason; after a long discussion with my RD Nurse. I wasn't on any other medication so there was nothing else that could have caused it so it was pretty obvious that coming off it may help; everyone reacts differently to medication however and it is supposed to be a rare side effect.

Please don't struggle with this, your RD nurse is there at the end of the phone for just this kind of thing.

Take care,

hugs

Ruth

Pollymolly profile image
Pollymolly in reply to Ruth273

Thank you Suzanne and Ruth for your replies. My depression and medicine issues are really complicated.

I'm on duloxetine for both pain (when I was initially diagnosed with fibromyalgia) and depression. It's so effective for pain I don't want to swap to another antidepressant.

But I do think the sulfasalazine has changed the nature and intensity of the depression. I wish I'd explained more to the RA nurse, but I'll call them and see what they say. She said to wait another 6 weeks, but I can't afford to keep feeling like this.

I'm not sure my GP will be much help ...

dgray78377 profile image
dgray78377

I am sorry to hear you are experiencing this but I am glad to hear that someone else is having the same problem that I am experiencing. I have been very depressed lately and I have never felt this way before. I have been on Sulfasalazine for awhile now and noticed no improvement in my condition either. I brought this to my doctor's attention and he stated this drug supposed to work well with Methotrexate. I beg the difference. Stay strong and pray a lot as I do to get better. Love.

My rheumatologist gave me the same tablets I went into depression like a bolt of lightning stopped after two weeks I go bact Wednesday to she them just getting my head together after 5weeks they think it all in my head and boy it was

Yes five years ago I was put on Sulfa by my GP bevause he was sure I had RA and I couldn't see the rheumy for four months. I didn't know about side effects and didn't really read the blurb - I was just desperate for the pain to resolve and terrified of having RA after reading up about early erosive damage etc.

I've had many drug reactions since but Sulfasalazine did put my mood down and gave me what I can only describe as an eggy feeling. After two weeks my GP raised the dose and my neck swelled up and ears got lumps and then I got a violently itchy rash from head to toe! So that was that - no more Sulfa. It was only after I stopped that my mood returned to normal and I realised how depressed this drug had made me feel too.

Adelaide1 profile image
Adelaide1

Stop taking it right now! It is a rare side effect, but I had it and was really depressed very quickly...unlike the anxiety I am prone to,this was proper deep depression. When I emailed my consultant she told me to stop taking it.

Ranjmcl profile image
Ranjmcl

Thanks for this post. The RA nurse has said it might be the next medication. I suffer from depression since I was 15 and finally (I'm 48 now) stablish. So I don't want anything to change that

Be honest about your depression otherwise other doctors will not know. So when a new drug is given say what other problems you have. Don't hide them. Having said that, your RA person should have looked at the meds you are on to see if there would be any problems. The system our GP uses checks it automatically. So I head for her to see if anything comes up

My advice : make an appointment with your GP asap to talk things through. They are likely to get a better response from your RA people

Good luck with both the RA and the depression.

jayh profile image
jayh

Hi I came off Sulfasalazine for the very reason that I became depressed whilst taking it. I know the RA in itself is depressing but in my case it was definitely that particular drug and my mood improved after stopping x

aristojune profile image
aristojune

Hi Pollymolly - Ive been on sulfa for nearly 5 years and hydroxy for almost a year - r a much better but...I can relate to the depressive feelings you having. About 4 years ago started to get weepy and then thoughts of dying crept in at the oddest moments! There had been big changes in my life, my husband died and about a year later I retired so put the tears etc down to that but I as I had never suffered with depression it hit me really badly. I'm now beginning to think that maybe the medication has more than a little to do with it so think I may mention it to my GP but as I'm really happy with my medication not sure if I want to change it.

ripecherries profile image
ripecherries

Yes, sulfasalazine made me very depressed, to the point where I couldn't even talk to my own family. I am naturally a bubbly, chatty person but I became so low I couldn't even talk. Am off it now and back to my old self.

Pollymolly profile image
Pollymolly

Wow, I'm so sorry others have had this experience but to be honest I'm pretty relieved to think sulfasalazine may be to blame for all this. I've been avoiding people because of anxiety and depression, including not going to work. I've even been too anxious and miserable to go get the blood tests I'm meant to have. But now I have some hope that I might start feeling better if I come off it. It's too soon to know if it would have helped the RA yet, and I'm having a bit of a flare at the moment in any case. Maybe I can go onto something else instead.

I hope this doesn't put others off trying it though - I understand this is actually quite rare. But it's something to watch out for I guess. Had I known, I would have been in touch with the RA clinic as soon as I started thinking about dying!

X

sames profile image
sames

Had to stop sulfasalazine after 2 month very bad rash allergic to the med I think it is a horrible drug it is a combination of an antibiotic and sulfa

Mall profile image
Mall

I was had very low mood when on 6 tablets of sulphasalazine but put this down to problems at work, lack of support, bullying. When I went onto methotrexate in combination my sulpha was reduced to 4 tablets. My mood lifted noticeably. I remained on 4 daily until I was prescribed enbrel too. As my symptoms improved dramatically I stopped taking sulphasalazine completely. My decision not my Rhuemy, he thought I should stay on it but accepted my decision. When I cut it out completely I did not notice any further mood change.

Thaistcb profile image
Thaistcb

I've been feeling the same thing. I've been taking 6 pills a day for more than month and started having panic attacks and vivid dreams. I decided to get into therapy, hopefully it works.

kkmw profile image
kkmw

I appreciate this is an old post but wanted to put my two cents in. Sulfasalazine is essentially an antibiotic + aspirin. Antibiotics can wreak havoc on your gut/microbiome and there is extensive scientific studies relating to the gut-brain connection. Mess with your gut and your mental capacities can be affected too. This may help to explain why some people feel depressed or anxious whilst taking this medication. It’s also worth noting that Sulfa can affect folate levels in the body, leading to a deficiency. Some of the symptoms include brain fog and irritability so it’s worth taking a supplement to counteract this (best to take folate rather than its synthetic form, folic acid).

Oceanbound8 profile image
Oceanbound8

I have almost the exact experience! I am a happy and mostly healthy 36 year old with a great life. Never suffered depression as far as I know, no mental health diagnosis.

After starting on Sulfa for crohns (was getting arthritis symptoms) I started feeling off/not myself. My partner noticed and was really kind about it, but that made me realize it wasn’t just in my head.

I see it’s super rare for sulfa to have this side effect but nothing else in my life has changed. And my dose is sulfa is very low.

Interesting and hopeful to see others go through it, if I know it’s just the drug I can try to “mind over matter” my way out of it maybe?

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