Has anyone switched from Methotrexate pills to the injections?

Yes, the Methx pills made me nauseous and have diarrhea. The injections made those symptoms much less severe ( I also suffered hair loss and extreme fatigue with both pills and injections but it was so much better on my digestive system to do the injections.

Hey PamelaB10! Thanks for reaching out. I thought this article on MTX might interest you. https://rheumatoidarthritis.net/treatment/methotrexate/ I hope other community members respond with their experiences.

I personally had the same side effects as you. I switched to the injections as well as a folic acid supplement (through a prescription from my rheumatologist). I like them a lot better than the pills because I don't have as much nausea or headaches.

I would suggest speaking to your doctor to find out what time you should take the injection. I know a lot of people (myself included) can minimize the side effects by taking the supplement and injections at specific times.

Please keep us updated, all the best! ~Monica

When I was early into my RA diagnosis, I used methotrexate. I began using pills. I had lots of issues with nausea and general yuck!!! Poor appetite and exhaustion. I switched over to the injectable methotrexate to see if it would reduce nausea, the yuck, stomach pain, etc. I am not one who is afraid of needles, but I was a bit nervous about the injections. But, you use a small needle and you learn the most effective way for you. Unfortunately, it did not work as well as we had hoped and I moved to biologics.