yuflyma - adalimumab : Has anyone had experience with... - NRAS

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yuflyma - adalimumab

skinclinic profile image
10 Replies

Has anyone had experience with the Biosimilar Yuflyma ( Adalimumab)

I’ve been having fortnightly injections for the last 2 months

I was on injectable methotrexate but became quite ill with it after 2 yrs use

I’m now going through a terrible flare in my hands wrists fingers knees ankles and shoulders- in so much I cannot walk , dress or even hold a glass to drink - far worse than in the last 5 years that I’ve encountered

Am I being impatient - how long do I need to wait to know if it’s going to be effective or not ?

I do have a hospital appointment this Friday to see the rheumatology nurse specialist… but guessing I may be told that it’s going to take longer to be effective but I’ve had no relief at all so

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skinclinic
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10 Replies
Tealblue2 profile image
Tealblue2

hi.

I’m almost in the same boat as you. I’m about to have my 5th injection next week. I was in a treble state a week or two ago, until I had the 4th injection- that seemed to turn the corner for me - but I had to massively increase the steroids to get me there. But this last week I can walk and move more than I have been able to in 3 months. Like you methotrexate made me very ill, then coming off it made everything worse.

I still have some swelling and am finding that my hands and feet are painful at night. But the improvement is amazing considering the time scale.

I really hope things get better for you soon!

Theoddjobman profile image
Theoddjobman in reply to Tealblue2

I am really encouraged by your reply. I take methotrexate injections and now yuflyma also fortnightly. I have been feeling worse in the first 4 weeks. Will persist now in the hope of improvement.

Tealblue2 profile image
Tealblue2 in reply to Theoddjobman

I felt worse before I got better. Fingers crossed for you!

skinclinic profile image
skinclinic in reply to Tealblue2

Thanks Teslblue2 . Yes I do hope it will kick in soon … To date this is the worst and most debilitating bout of RD that I’ve ever had

oldtimer2 profile image
oldtimer2

I had almost instant relief with adalumimab (sorry!) but other people have said it takes longer. You could ask for a short course/injection of steroid to tide you over until it starts working?

skinclinic profile image
skinclinic in reply to oldtimer2

Hi Oldtimer

I’m glad you had early relief… and I will be asking my rheumatology nurse specialist this Friday for more steroids .. I have been taking 2 pred daily but it seems I now need to move on to a higher dose for awhile

Thanks for replying

RAat13 profile image
RAat13

Hello.After 2 months you should've seen some difference but it can rake 12 weeks, I have no positive for that drug as I had a horrible complication from it. What has your Rheumy said?

skinclinic profile image
skinclinic in reply to RAat13

Hi RÃat13

I did hope that I’d get some relief especially as this has being going on since August last year and I was without RÃ meds for 6 months ( due to Latent TB antibiotics )

Maybe I’m being too optimistic in a 2 month time and also I had a dental abscess and the tooth extracted which really kicked things off .

5 years ago I had a dental abscess and a tooth extracted because of it ….. and it was then that my RÃ was initially triggered .So maybe my current debilitating flare has been induced by the same abscess/ extraction. And it’s probably been too bad a flare for my new Biologic to ge effective yet

Thanks got taking the time to reply to my question

RAat13 profile image
RAat13 in reply to skinclinic

Anything can trigger a flare especially infection, I had a toe removed in January 2023, I had an infection that was caused by the head of damaged joint trying to make its way out.. which caused an 8 month flare and ILD, I've just realised I've confused 2 biologics, the adalimumab (Humira) did work for me for a few years before it stopped altogether, abatacept is what caused problems for me,.. I'm so sorry!I would speak to your nurse or consultant and ask for some advice..

I hope you start to feel better.

I was put on Rituximab in August last year after the worst year of my life and it's given me life back, I did have to learn a new normal again but I'm well and pretty much in Remission after 22 years, ❤️

skinclinic profile image
skinclinic in reply to RAat13

Hi RÃ at13

Thanks for your reply

Glad to here that you’ve got your life back after 22 years

Thanks for your well wishes - hopefully I will get some help tomorrow when i attend for my rheumatology appointment

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