I was just wondering if anyone has experience changing the time they take methotrexate. I'm considering switching from morning to evening as it makes me feel a little nauseous during the day, and I think I might not notice this so much while sleeping. Any thoughts? I've been taking 20mg for seronegative inflammatory arthritis for about a year and am currently in remission.
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Jacojudy303
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i take it in the evening, so I sleep through side effects. I did once have to hold off, as hubby was waiting on a covid test, it came back negative, so I took it that morning. Ended up spending the day in bed utterly fatigued. Yet I don’t get fatigue or nausea taking it at night.
I now take mine just before I go to bed. It's really helped with the nausea. I have the odd time when I'm not so good, but so much better than I was when I took it in the morning. It's been well over 7 years since I changed.
I split mine and take half with breakfast and half with tea, this helps me and is accepted by rheumatologist as good practice to keep med viable for me. I also take Baricitinib every morning.
I inject early evening. I find that the side effects (usually tiredness rather than nausea) kick in 24 hours later so I feel tired the following evening which is better than in the morning, I suppose 😁 I started on tablets and took them after tea as I took my Hydroxychloroquin after breakfast.
Hi, I have pre-filled injection pens and do that before bed as I find I feel really tired. When on tablets, I took with my meal in the evening to lessen any nausea.
I take it late afternoon, when I'm not taking any other medication. The following day, similar to others, it has a slight detrimental affect. Good luck.
I changed due to same reason . Take mine half way through an evening meal. Then a glass of tonic water after my meal and the nausea goes away almost immediately.
It use to make me feel nauseous so I started injecting after my evening meal which is much better. Sometimes it stings when I inject but hardly ever feel nauseous now. Keep hydrated too. Good luck 👍
I also was recommended to take methotrexate last thing, though I don't seem to get nausea. I wouldn't worry about changing the time you take it. I occasionally move my medication day if I need to.
Thanks for the advice everyone. Tried taking it last night. Much better on the tummy. I was a little slower than usual when I ran this morning but I reckon that’s cause it’s freezing here in London 🥶
I was doing the injections in mid morning, and the very painful gut reaction started just as I was going to bed and kept me up all night. But it would have been just as bad to have the pain during the day, or waking up with it, or when ever, so I stopped. But for 5 months I had no problem doing the injection mid morning.
Hi I split mine as I had the most awful nausea so Rheumatology nurse suggested trying this. I take half at lunchtime and half with dinner and it seems to have helped.
Hi, sorry to hear you’re having problems, because of sickness I was informed by the nurse team that I could split my dose to half in the morning and half in the evening and that I could increase my folic acid to every day except methotrexate day which has resolved my problems
I have always taken mine just before bed and found this the best time, some times i am still off colour the next day but the worst is usually over by the next day.
I'm on MTX injections, for me I take anti sickness meds (prescribed) half hour before doing the injection. Do my injection before bedtime to sleep through worse symptoms.
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