Experiences with

Humira

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.

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.

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.

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 ??

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

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.

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

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.

The nurse mentioned adding hydroxychloroquine or switching to humira, i don't like the side effects list of either 🤦‍♀️ eye problems or cancer. Any advice would be appreciated.

hi all I started humira on 7/2/24 after cimzia failing after three years. Iv had 5 injections so far and iv still not seen any improvement at all. I’m allergic to methotrexate and the other dmards they try us with. what has your experience been like, in terms of success.

I have had 1 injection of generic humira and my smell has come back for 5 days now !!!!!!!! I do still smell smoke also.

She put me on methotrexate, hydroxycloroquin, and Humira. I'M struggling with side effects. But also afraid to give up. Anyone else been on a mix of drugs like this before?

Anybody else had or having the experience of being forced to change from Humira to biosimilar Yuflyma? I’m lucky to be in good health and chemical remission from RA thanks to a MTX/Humira regime for the last 8 years.

I also have to inject a drug called Humira. This drug has many risks involved including cancers. Due to blood being in my urine I yet again am being investigated to rule out cancer. anyway I went round my fathers for Father’s Day. I was sweating abnormally and feeling sick.

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.

( 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 didn't have any major skin reactions, unlike previous biologics Enbrel, Humira which I couldn't continue because of skin reactions. So I am now wondering if this change to Tyenne is causing an allergic reaction/side effect.

I have ulcerative colitis with inflammation of the cecum that may be due to lupus or meds. Not really sure. I’m advised to take something similar to one of the drugs questioned to reduce inflammation. I have ckd 3b and don’t want to make it worse. Trying to determine which is better.

Was currently on Humira and was still having pain, stiffness and my inflammation was up. Starting Rinvoq next week