No marked improvement after 7weeks: Just enquiringly... - NRAS

NRAS

37,276 members46,139 posts

No marked improvement after 7weeks

Mollieharry profile image
16 Replies

Just enquiringly how long oral methotrexate should take to work.im on my 8th wk of taking it.starting at 7.5mg and now up to12.5mg.will be at 15mg come Monday.i also take 3mg(6tabs) of sulfasalazine daily too.this initially worked on its own but methotrexate was added when it stopped working.knees still very sore stiff and swollen.ankles and feet just really sore.

Written by
Mollieharry profile image
Mollieharry
To view profiles and participate in discussions please or .
Read more about...
16 Replies
allanah profile image
allanah

I think most doctors say give it at least three months. I know that's hard when you are in pain and tired. Maybe call your rheumy helpline and ask if it's possible to have a steroid to tide you over, my rheumy did. The higher dose should also help.

Good luck x

Mollieharry profile image
Mollieharry in reply toallanah

Hi Allanah,rhuemo gave me oral steroids the beginning of December so I could go on holiday without being miserable and to give meds time to kick in.unfortunately she tapered them down and stopped after 4wks.when cutting down pain increased.dont think they would put me back on them as soon.

allanah profile image
allanah in reply toMollieharry

Might be worth ringing them still. I got injections xxx

Mollieharry profile image
Mollieharry

Fingers crossed kitty.thanks for replying.out of curiosity,do you know if the injection methotrexate works better or has less side affects?

allanah profile image
allanah in reply toMollieharry

The oral can make some people nausea. The injection bypasses the tummy so tends not to cause nausea. But then you have to inject x

NeonkittyUK profile image
NeonkittyUK

Hang in there Mollie and you should notice improvement soon. I did after ten weeks. x

HappykindaGal profile image
HappykindaGal

Unfortunately, finding what works can be quite brutal. Mtx may not work in the end by itself. I was told that each DMARD is tested for a minimum of 3 months before adding something else if it doesn’t work. I took oral steroids for over 2 years to support 20mg mtx, sulfasalazine. Already given up on hydroxy as was pointless. At 2 and a half years and finally off steroids, was almost immobile still, so approved for Benepali. I’m now in a very different place.

That’s probably not what you really want to hear, and I hate that due to funding mainly, all the cheaper stuff is tried first when biologics appear to help immensely. Steroids will mask the disease to some extent which is not always a good thing.

I hope you find what works for you very soon. It’s horrid feeling so rubbish all of the time.

Floralqueens profile image
Floralqueens

Hi. Stick with it, the impact from the MTX takes about 3 months to kick in. My rheumatologist gave me a steroid injection to ease the pain in the meantime. Maybe worth ringing your rheumatoid helpline in the hospital and explain your pain and hopefully they too will offer you a steroid injection 🤞🏻.

MagsLough profile image
MagsLough

It’s the other way round I think. Because the injection bypasses the stomach and you don’t lose some of it it to your digestive system etc

in reply toMagsLough

I was put onto injections because I couldn’t tolerate the higher dose in tablet form though. Perhaps my post should have said tolerate instead of have. 😊

MagsLough profile image
MagsLough

It took around 3 months for me and during that period I was also on a lot of naproxen to help get the inflammation under control. Your mtx dose is being stepped up quite slowly I think so hang in there

Joy_1 profile image
Joy_1

I was told it takes about 12 weeks. And for me yes it was about 12 weeks.

BonnieT profile image
BonnieT

Started almost a year ago. Building the dose each time I visited the doc three months apart and new bloods drawn. I’m at 25 MG. splitting the dose 5 tabs one day and 5 tabs the next. I’m ok most of the time but pain can hit me anywhere making me either miserable or just uncomfortable. Right now my jaw is bothering me and may go to dentist to check it out. Last week it was my chest. Prednisone when there’s a flare. Hate it. Good luck with yours.

lKeith profile image
lKeith

Mollieharry

Hi, Methotrexate is a long term med and doesn't always show you any benefit immediately, try to stick with it.

IKeith

Nanna71 profile image
Nanna71

I've been on 10mg, then 15mg MTX total of 8 weeks. However, weaning off Prednisone too. It is hard to tell if the MTX is working because the Pred. works very well for me for pain. I'm going from 15mg Pred. to 10mg. tomorrow. Then after a month, nothing I think. The MTX is supposed to have taken over the job. My Internist is working my meds. and I think it takes a LONG time to get it right. Pain is surely the hallmark of RA. Hope my limited info is helpful.

Mollieharry profile image
Mollieharry in reply toNanna71

I would have thought it would have been better for me to stay on the prednisalone for more than 4wks,at least enough time for slight improvement,but this wasn’t to be.im sure my rhuemo nurse had a reason for this.so from all the comments i’m just going to have to put up with the pain and wiped out feeling a bit longer to see if adding the max is going to make a difference.thanks everyone for replying.

Not what you're looking for?

You may also like...

Methotrexate Cessation after contracting covid

Hello everyone… I tested positive for Covid this morning and have fairly manageable symptoms… just...
Jadite profile image

No improvement

Hi Guys, Thank you all for your comments and advice. I really appreciate it and it helps hearing...
Angie2212 profile image

Penicillin

Over the weekend I got a very sore throat, called ADOC and at the appointment I was given...
WiltonT profile image

No Flu Jab!

I have just been refused a free flu jab by the receptionist at my GP Surgery. I have had them...
AlexGrealis profile image

Which drug next

Not on any rheumatoid medicine. Tried one dose of Humira in December. Ten days later came out in a...
28maggie11 profile image

Moderation team

See all
KateL-NRAS profile image
KateL-NRASAdministrator
Donagh-NRAS profile image
Donagh-NRASAdministrator
Nicola-NRAS profile image
Nicola-NRASAdministrator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.