I have changed from Methotrexate tablets to injections. What a difference...no more daily nausea thankfully. Injections easy to do too. For me this has really worked. I can see why pills are prescribed as injections must cost the NHS a lot more. Certainly worth considering if you are suffering from nausea as I was. Blomps
Methotrexate tablets or Injections: I have changed... - PMRGCAuk
Methotrexate tablets or Injections
That’s good news Blomps, are they preloaded? Keep us updated on how you’re doing please.
Kind Regards
MrsN
Certainly will do.
Yes preloaded injections and very simple to use. Blomps
Pleased to hear they are working for you.
Just about to start Methotrexate - should have been last week, should have been today and have put it off until tomorrow. Tablets.
I haven't had any noticeable side effects from taking my methotrexate tablets, but I can understand your reluctance - I was worried at first. I do suggest that you take your tablets at night as I did feel knocked out when I took them in the morning. I set my alarm for 10 p.m. every Friday to remind me.
You’ll do it when you’re ready! 😉
It is good to hear that this method of administering Methotrexate suits you better. Keep in touch.
Great positive news , really hope it keeps working for you.
Keep us posted as you experience may help others make a choice on MTX or give them options to ask about for the way they take it in the future it they suffer similar side effects to you.
It might even help some people have the opportunity to continue with trying MTX to help them in their creditors if they have only tried oral treatment.
Hi there, Certainly will do as its so important to share experiences. So far the change to injections is 100% positive. Apparently tbey are also more efficient than tablets. My Specialist is considering increasing the dose also to 20mg from 15 to help get off the steroids sooner. Steroids have sent Diabetes figures into orbit after good control for years without medication. Now using Insulin and Metformin again so to get away from Steroids will be good as long as its done without encouraging flares in Polymyalgia. Time and patience are the keywords a day at a time. Thanks again Blomps.
Except even higher dose mtx won't necessarily replace pred. It is quite unusual for it to do so - I wonder what makes them think so?
I dont think is is to replace the Steroid but assist in getting off sooner. Blomps
That's what I mean - you will get off pred when the underlying autoimmune disorder that causes the symptoms we call PMR burns out and goes into remission. Nothing you do will change that duration - methotrexate or not. It MAY allow you to manage on a lower dose in the meantime but it won't speed up the process.