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Have you had side effects from methotrexate?
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PollyP
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PollyP
Last activity on 01/02/2023 at 10:06
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12 comments posted | 11 in the Rheumatoid arthritis Forum
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Hi everyone, I've been on 15mg of oral methotrexate each week for a while now, but my rheumatologist has decided to switch me to methotrexate injections at the same dose to increase the effictiveness and possible decrease side effects.
Has anyone on here also been through this? Did you see any real improvements in effectiveness? Did you side effects go down or did you see more?
Thanks for any feedback x
EmmyJane
EmmyJane
Last activity on 10/05/2023 at 20:18
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15 comments posted | 13 in the Rheumatoid arthritis Forum
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@pollyPP I've only just started methotrexate and I take it orally, so I can't really help you unfortunately. I'd be interested to hear peoples" experiences though on it. So far I haven't had many side effects yet besides a bit of nausea that passes.
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EmmyJane
EmmyJane
EmmyJane
Last activity on 10/05/2023 at 20:18
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15 comments posted | 13 in the Rheumatoid arthritis Forum
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I thought I'd come back on here for an update I guess. I've been taking my methotrexate tablets for several months now and the pain has gone away. It's been fantastic overall, but something I've been truly struggling with is fatigue. It's been very difficult. I also feel like I've been in a more negative mood since before I started taking it. I don't really recognise myself anymore, I used to be very upbeat and active...
Could this be from the methotrexate or is it from the RA? My low morale worries me a little and I feel guilty for making my loved ones suffer because my chronic fatigue...
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EmmyJane
Courtney_J
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Courtney_J
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Last activity on 13/10/2022 at 16:47
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@EmmyJane Hello EmmyJane, thank you for keeping us updated on how you're doing on methotrexate. If you haven't seen it already, one our Ambassadors, @richard0804, helped us write an article on methotrexate, its use and side effects a few months ago. You may find it helpful: Learn more about methotrexate!
Has anyone else experienced extreme fatigue and mood changes whilst taking methotrexate? If so, how did or do you cope with it?
@yesyes @Rafa76 @Juliana @Mairi1956 @Scoobysue1 @Layton @lizshi @noelynn @JRL1965 @dilizjo @MarkOrton @Un4getablefox @Samsung12 @Bobbiegirl @Aideen61 @nanvanham @Susiemaxwell @earthspirit @Mog789
Feel free to share here!
Take care,
Courtney
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Courtney_J, Community Manager, Carenity UK
BoxWood2
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Last activity on 19/06/2021 at 12:14
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6 comments posted | 3 in the Rheumatoid arthritis Forum
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@Gizzidoggie
Hi sorry to hear you are having problems with diverticulitis and Methotrexate. I too have diverticulosis but fortunately have never suffered any adverse affects from taking Methotrexate. I do take Folic Acid twice a week, always 3 days after Methotrexate and have very few side effects. I still have the occasional flare-up with pain in my hands and shoulders but on the whole my symptoms seem to be well controlled. Ive been on Methotrexate for 3 years now and hoping I may be able to reduce the dose soon. If you are not taking it , perhaps Folic Acid may help you. Worth asking your practitioner.
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Christine Lackey
Mandy59
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Mandy59
Last activity on 19/11/2024 at 19:23
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I started methotrexate tablets in 2002 and found it made me feel very ill. Stomach cramping & vomiting. Bruising, nose bleeds, headaches, hair loss & bleeding gums / tooth loss.
ln 2016 l was changed to injections but due to my pain/swelling in my hands l found it hard to administer the injections myself so had to attend the hospital every week for a rheumatology nurse to inject me as my doctors surgery said they were not allowed to do it.
ln 2019 l was given the metoject pen & things are so much easier to inject but l still suffer side effects & if l didn’t have to take it l wouldn’t. Think it’s a horrible drug (if l don’t take it l can’t have biologic infusion)
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M.Flood
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Joanne50
Joanne50
Last activity on 26/07/2020 at 20:35
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1 comment posted | 1 in the Rheumatoid arthritis Forum
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Hi im Jo. Ive been on methotrexate injection and cimzia injection for about 2 years now to treat inflammatory arthritis. I also have fibromyalgia and ulcerative colitis. After having a growth removed from my shin 6 weeks ago i have just been diagnosed with Bowens disease. Ive been told people taking methotrexate have a higher risk of skin cancer . I have been told i have to come off my injections for 4 weeks whilst i have treatment but am petrified of the pain coming back. Has anyone experienced this?
Jo