we’ll finally saw a rheumatologist to be told I have PMR and Osteoarthritis and Rheumatoid arthritis. I’m currently on 13 mg of pred and have now been given methotrexate tablets I take 6 every Thursday. A nurse is coming to show me how to inject myself instead of me having it via tablet. I was just wondering if anyone has it this way .
methotrexate via injection : we’ll finally saw a... - PMRGCAuk
methotrexate via injection
Many - have a look at FAQs- and in particular MrsNails story with MTX
HI DL has pointed you in the direction of my Experience & l much prefer the Metoject than the tablets - they are so fiddly as they are so small & l’m on 25mg MTX so that was10 tablets!
It also means you will absorb the full dose & avoid any gastric side effects ie Nausea.
Good Luck 🍀
MrsN
thank you for your reply👍
Hi Shaza123, I moved from the mtx tablets to injections after 2 weeks as I had awful stomach pains. Hopefully you'll get used to doing the injections quite quickly. They are quite straightforward to do as in a pen form. Like you, I also have other diseases, so if my hands are flared up I can find getting the lid off the injection pen a bit fiddly but still able to do it.
My biggest advice is to use a different place to inject each time - I rotate from left thigh, right side tummy, then right thigh, left side tummy. And don't go close to tummy button. I also put a plaster on the injection site but it's prob not necessary.
It makes you bit more prone to infections, especially combined with pred, but is ok. I feel a bit rough for 24 hours starting 8-10 hours after my injection, but play around with timings of injection to make sure I sleep through a chunk of that.
Good luck, perseverance is key with this drug. It'll be harder at first but once used to it and it starts helping, you'll manage loads better.
the methotrexate I only took in tablet form but it never worked for me. But now I inject myself with RoActamara and am now down to 9 mg which is good because the last few years when I get down to 10 mg I have severe flare ups and end up in hospital. Thank god this new drug is working I’ve been on steroids since 2017
I took Methotrexate by injection. I took it because I was told it would not bother my digestion nor become nauseous. I was quite fearful of giving myself an injection which turned out to be the easy part. I had so many other side effects that I could not tolerate it. I hope it works for you. The best to you.
Hi I take it in tablet form. It can have quite bad side affects initially but they do wear off ......Good luck
I started on oral but changed to sub cut injection a year ago. I dont get much nausea now and Im down to 5mg pred. Its a bit of a pain having my bloods done every 3 months but that would be the case for oral as well so no difference.
On balance I'm happy with the MTX, seems to be working for me.
I've changed recently from oral to Metopen. Very happy with it. Was nervous first time but didn't feel a thing. I have had my 5th this morning and hoping that my slight overall improvement in my symptoms is down to the new method.
yes, I inject every wednesday evening, it is so easy, do not get worried about it, once you have done the first one you will be fine xx
Hello Shaza123, your story resonates with me. I have been diagnosed for 3.5 yrs w/PMR. On varying amounts of Pred., and resisted MTX for 1 yr, until five mo. ago. By thereafter many Pred paring flares and discouragement, I said yes to MTX, currently 17.5mg tablets wkly, and 4mg Pred, and relatively pain-free for 5 mo. I worry about reducing Pred further, but that's the objective with MTX. We will see. I will follow your progress if you keep posting.