Experiences with

Humira

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

Since I last posted its now been confirmed macular degeneration has started the right eye has a lot of scar tissue, also CNS involvement Been put on Rituximab as the replacement of Humira. Sadly I contracted covid just days after the infusion .

( 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.

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.

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.

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?

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

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.

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 was given Humira and Benapli but infortunately had unpleasant side effects. My then consultant was very unpleasant , PALS stepped in and I had anew consultant .

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.

But because of this incidental diagnosis, my rheumatologist took me off my Humira until the haematologist said it was safe to continue. Which it is. But over 2 months untreated left me really struggling so I was given a big steroid shot to ‘keep me going’ until I get back on the Humira.

Or possibly it would be similar to reducing when using Actemra or Humira? Or should I just follow the usual DSNS method I've used before reducing .5 mg each time? (By the way, in the States, you can get this drug free from the company, Kevzara Connect.

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

recently started humira in feb but still in pain and agony in joints and eyes are flared losing lots of hair since starting humira was on cimzia before and that gave me good three years of relief

Hi Been on methotrexate and sulphasalazine since last year so newly diagnosed but not under control and was put forward for Humira , however because of a previous issue some years ago nothing related to RA I’m not going to be suitable for biologics at the moment so Gojng to start me on Filgotinib.