Experiences with

Humira

Hello, I've just started on Yuflyma.Previously on Humira I developed odd veins on my back and was taken off Humira and put on Rinvoq which caused liver damage and so was taken off Rinvoq in Sept. Had temporary Kennalog injection, and then put on Yuflyma.

I started injecting Humira fortnightly in July. I also take MTX. For the last few weeks I have been experiencing stabbing pains in my thigh, also numbness in my lower leg. I have read about this on Dr Google, which I know is probably not a good idea. It has frightened me to death.

I started fortnightly Humira jabs last July, I also take weekly mtx tablets. I have started to get shooting pains in my right leg plus occasional tingling. Has anyone else experienced this? Know I shouldn't read Dr Google, but I did 😞. Apparently this may be a rare side effect.

I just visited with a uveitis specialist, and she recommended Humira (a non-steroid treatment for inflammation and potential autoimmune disease) as treatment for recurring bleeds due to myopic CNV. Has anyone tried and succeeded with this course of treatment?

I have been on Humira for 19yrs and in October my Specialist asked me to try Amgevita. I agreed and have had 1 course so far but was wondering if anyone has made the same change and if so, any side effects? Any information would be helpful.

I’m on Baricitinib & husband Humira. Does anyone know if correct as my GP doesn’t know about the rheumy drugs.

has now apply funding for me to get JAK inhibitor ( as biologics don't seem to work anymore for me) Might take a few weeks/months before I start new treatment though 🤞🤞hopefully JAK will work for me Hello,I am on tociluzimab and leflunomide but it's not working anymore .( also tried previously humira

Hi all, I am starting Enbrel this week after having been on humira for 6 mos. I had no bad reactions with humira- it just was not controlling my RA. I guess I am not too eager to take my first shot for fear of getting sick.

It was thought that biologic drug Humira. caused it, but unfortunately after stopping it, the Cutaneous remained. I'm very lucky to be treated at Guy's as their care is excellent. .

Apparently my Humira may also be causing a lot of these issues. He advises to stay on it whilst I do the B12 because if it stops the frequent urination again I’d know the Humira isn’t causing it. However if I keep injecting b12 and quit Humira I won’t know what’s causing it.

I saw Rheumatologist again just before Xmas and she said she'd like me to try Yuflyma which is a new biosim of Adalimumab, didnt have a great experience with Humira but I've agreed because there really isn't any other option on the table.

Hi I take Simponi 100mg injection every 4 weeks, this is my second biologic as I was previously on Humira but it stopped working (I have AS). I constantly get eye infections and bacterial skin infections and currently have an access on my arm that is extremely painful.

In addition, I am on Leflunomide 10mg, prednisone 7mg and Humira for 15 years without a problem. All my labs look great except that my enzymes have started to increase in the last two years. I also have been experiencing more flares, hot flashes and brain fog.

We can't seem to get them under control and doctor wants to try Humira. Is anyone using this medication? Just wondering what side effects you are experiencing and if it helps. thank you for your time and hope all feel better soon.

Should I take Methotrexate and Humira this week? I have continued with steroids 4 mg daily and statins 10 mg daily

started humira in feb 24, and still no improvement from humira on my ra. Additionally this is my daily hair loss three weeks into starting. I literally have a mouse’s tail left now. Is this normal ??

I’ve been on them for 15 years, but the last 3 I’ve had this issue. anyone else had these side effects with Humira? If so when did they start? Apparently it can cause Megaloblastic anaemia

Did all my labs, jabbed me with Avastin, kept me on oral prednisone, and started me on humira. Eventually tapered steroids and my problems were gone until end of March/beginning of April 2022.

( I have had Humira, ritux & Filgotinib now so not much choice left for me ) My Rheumatologist says “Ritux is slot cheaper now” so will try!

I had bad side effect from Humira injections( constant uti s, Encerecept caused chest pain ( probably bad acid reflux). I refused Methotrexate . Apart from steroid caudal injections and a short course of Prednisilone I have had no rheumatoid drugs at all for 2 years.