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Methotrexate injections Options
Maggie11
#1 Posted : Monday, March 17, 2014 5:04:51 PM Quote
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Joined: 2/26/2014
Posts: 8
Location: Essex
Hi, I've been on Methotrexate inj now for 5 week, my dose has increased in the last fortnight. I've been suffering with horrible headaches about 2 days after injecting , almost like strange sensations in my head and I get very cold with it! Has anyone else experienced this?
Xx
Little Miss Sunshine73
#2 Posted : Monday, March 17, 2014 8:47:22 PM Quote
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Joined: 3/29/2013
Posts: 106
Location: Surrey
Hello Maggie,

My metjet injections have now been reduced to 10mg & am lucky to no longer suffer side effects. When I was on 25mg I did get extremely tired on the day I injected & would fall asleep very easily. The only side effect I still suffer from is with the sun as I get a tingling feeling over my skin if I have been sitting out without sun cream.

Have you got a Rheumy Nurse you could call or a support team?

Louise BigGrin
Rebecca D
#3 Posted : Tuesday, March 18, 2014 10:27:31 AM Quote
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Joined: 12/4/2009
Posts: 242
Hi Maggie

I know exactly what you are saying. I've been getting horrible headaches and the shivers for months now, two days after injecting. I am still on 7.5mg as the side effects have not got much better. I was advised to take 8 paracetamol on the day of injecting and for 2 days after. It has helped a bit. I really feel for you because it's bad enough dealing with pain as well as drug side effects. How much folic acid do you take?

Hope your side effects improve.
Best wishes
Rebecca
Paul Barrett
#4 Posted : Tuesday, March 18, 2014 12:49:47 PM Quote
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Joined: 4/24/2013
Posts: 703
Location: Hexham
My 4th dose of MTX by injection gave me such bad shivers and headache that I ended up in A&E. At that point I stopped the injections.

I am in awe of the side effects you guys put up with.
Paul Barrett

Hexham - Northumberland - Loads of spectacular walks - all I need now are the joints to go with them! :)

Enthesitis (2012)
Ulcerative Colitis (1990)
Maggie11
#5 Posted : Tuesday, March 18, 2014 9:15:07 PM Quote
Rank: Newbie

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Joined: 2/26/2014
Posts: 8
Location: Essex
Thank you all for your comments - I'm glad in a way it's not just me! I rang my CNS and have been advised not to inject this week and go back to lower dose next week. Hopefully this will help, although I'm a tad apprehensive as I'm just getting over a bad flare! Intake folic acid on 4 days of the week.
Xx
Maggie
Dorothy-W
#6 Posted : Wednesday, March 19, 2014 8:50:24 AM Quote
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Joined: 9/13/2010
Posts: 786
Location: east anglia
hi Maggie,i am on 25 inj mtx,the tablets took too long to get into my system been inj same dose now 4+years and yes the headaches/side effects are horrendous,i get very hot so I think I am wired up wrong,my feet feel odd for the 2 days and I get a real burst of energy about a hour after I jnj then I have to sleep maybe about 2/3 hours later for about a hour or so or I just feel so bad I cant function right at all,i have worked it out now so I know when to get home and lie down,i make sure I don't have must do's on that day, i take 6 folic now as I was so tired and had the hair loss thing,my nurse at the time advised me and I have been ok since but it still floors me for 2/3 days I just work through it but do have a full rest day every 3 days if I can,my family and close friends are good as they know if I say not today I mean not today and they back off,its just getting what works for you,take a look at what you eat too as I found too much of a certain something can contribute to the down sides, MUST use 50+ sun factor when on mtx,even if out and in all day when strong sun is out,i got caught out just didn't think and I got a skin reaction it was awful now I buy nivea kids it goes on green and dries invisible,have fun,dorothy
Rebecca D
#7 Posted : Wednesday, March 19, 2014 4:44:08 PM Quote
Rank: Advanced Member

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Joined: 12/4/2009
Posts: 242
Hi maggie

I was advised by the rheumy to take two 5mg doses of folic acid on two days before metho day instead of taking folic on 4 days a week. This has helped slightly with me. You could ask your rheumy nurse for some advice about that.

Hope your lower dosage controls your flare. You may need a bit of steroid to help you.
Best wishes
Rebecca
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