I've been on methotrexate 25mg since march and switched to the injection in August. The injection was great and was stopping the sickness but in the last month and half/ 2 months I've began getting reactions at the injection site. I've ran out of places on my legs to inject as there either really bruised or lumpy and red. It's also extremely itchy and my skin in going extremely dry around the areas. Is this normal or is it a sign the injections aren't for me?. The tablets made me extremely ill so I'd rather stay on the injection if possible. Plus i'm also on humira injection so there now becoming painful due to the bruising from methotrexate as I had to move my methotrexate injection to my humira leg because of the bruising and lumps.
Hi Amyx99x,
I have been on methotrexate injection since April and I have noticed some bruising. I start my shot on the right thigh, then right side stomach, left side stomach and left thigh. That monthly rotation works for me and so I don't feel the soreness and the bruising has gone down by the time I start the rotation again. I did that rotation when I was on orencia too and I'll let keep it up with the humira.
I have not noticed any lumps except the first 24 hours after injecting which I'd imagine is normal. I'm attributing the dry skin to the winter weather so I apply lotion all over.
Hope this info helps console abit.
I am on Etanercept injections and get bruising, redness, itchiness and swelling at the site for nearly a week. I've found moving the site the best so I do right lower thigh, left lower thigh,right upper stomach then left, upper thighs then lower stomach and by the time you come back to the same spot it's been enough time to heal. Might be a bit harder for you as 2 injections but my nurse said that as try and make them 3cm or more apart from the last site in that area.
Hope this helps.
Hi I have been on methotrexate for a number of years, I have been injecting myself for about 4yrs, I was told to inject in my stomach, I do get some bruises but not every time. Hope this helps. Regards Wendy
Ich injiziere mir MTX jetzt seit über fünf Jahren. Der GP hat mir beigebracht, wie man richtig injiziert, nun ja, nicht ganz so, wie er es wollte, aber wir haben es herausgefunden: oben am Bein, wie beim Dartwerfen, dann den Griff wechseln, ohne die Nadel zu berühren, und mit dem Daumen drücken. Ich habe auch Arthritis in den Händen, und ich injiziere langsam ins Gewebe, keine Blutergüsse, manchmal ein bisschen Juckreiz, aber nicht immer, etwa einen Zoll oder mehr pro Woche im Abstand. Die Tabletten haben bei mir nicht gewirkt, anscheinend wurde die Dosis nicht über meinen Magen aufgenommen. Es hat Monate gedauert, bis der Rheumatologe herausfand, warum ich keine Besserung zeigte. Bluttests gaben schließlich die Antwort. Ich nahm die Tabletten ein und ließ am nächsten Tag Bluttests machen, um zu sehen, wie viel MTX ich im Blut hatte. Es war sehr wenig im Vergleich zur verschriebenen Dosis.
I don't take MTX injections but have been taking Humira and I had very itchy , red and hard lump at site of injection a few days after I injected. I did tell the doctor
and also read on here to use ice before and after I injected at that site. Doctor said to try that and also to use cortisone cream after I gave the shot on the area
That did help a great deal. Itchy, hard lump were much less of a problem, redness present but that didn't bother me. Doc also said she could give me prednisone pill the day before and after the humira but I said no
Better to mention to your doctor though but I don't think the ice would cause any problem if you dont use longer than 20min and keep a cloth between your skin and the ice
Good luck, hope something helps
I had a similar problem with the injections and spoke to my Rheumatologist and the nurse and found that I was actually going partially into the muscle on my thigh rather than just sub-q as I was supposed to. Since then I make sure an pinch up a larger amount of skin to make sure I don't get into the muscle. I was told I could use my abdomen too, but I find that too difficult and can't get the needle in really straight like they told me too, so I just use different places on my thigh. I am on the same dosage as you. What did the Rheumatologist say about it?
Take care
I inject into my belly, where it's easy to get a good pinch of soft flesh. Just stay an inch away from the navel, and I was advised to go around it like the hands of a clock so you never hit the same spot more than once every three months (to avoid creating scar tissue). Might work better than the leg?
Welche anderen Nebenwirkungen von Methotrexat-Injektionen hatten Menschen außer Blutergüssen? Ich mache mir Sorgen, da ich alles neu bin.