ADALIMUMAB-AACF vs ADALIMUMAB-BWWD

I am a 40 year old female I have ankylosing spondylitis for which I receive injections of IDACIO (adalimumab-aacf) and low doses of extended release hydromorphone for the pain in my lower back and knees, but take no other medication and have no other medical issues I was on birth control pills from

The ugh is: I’m trying to work from home from bed after my second ever biologic injection (adalimumab aacf) feeling like I’ve been hit by a ton of bricks. That Humira (biosimilar) Hangover is no joke, good lord. My first injection, had some nausea and headache, but made it thru the day fine. But hol

Anyone know why Idacio was discontinued? I see it was discontinued on April 1 but I can't find any news about it. Going to the Idacio website gives a 404 error now.

I just had a follow up with my gastrointerologist and the majority of our conversation was about all or most insurances not covering Abbvie’s Humira. He told me Abbie has been preparing to stop servicing Humira for a few years now and with the patent expiring, this is the year they have done it.

First, I would just love to say that I am so excited I found this. Newer to Reddit. But the amount of information that I have read in this has helped me tremendously. I was diagnosed a year and a half ago. Been through methotrexate and prednisone and unfortunately, I have been in a flareup for most

I just wanted to share my recent experience with recapturing remisson if it helps. I had been in Hadlima induced remission for 11 months and experienced the worst flare of my life the week before I started my new job. I was bed bound three full days and continued to suffer an additional three week

Hi all, I have been taking Humira auto-injector pen for Chron's and hidradentritis supprativa for several years now. i have had almost no issues. January this year, I received a letter that my insurance no longer covers Humira. my doctor said they would submit a prior authorization for me to try

Hello everyone. I was diagnosed almost a year ago. my flair ups have been reduced thanks to Hadlima, but I still experience frequent flair ups. I have a mostly desk job but I find myself in such incredible paid from looking down at paperwork I sometimes have to leave mid day. I was recently contacte

Just an informative post for those in Canada, but more specifically Ontario. My dermatologist, when I first met with her regarding HS, put me on an oral antibiotic (Amoxycilin) and a topical (clindamycin). Personally, the topical did not work for me, but after a few months, she recommended I try a

I'm an ex-junkie (8 years clean this past december) and I started hadlima a few months ago and I swear to God, for like 2-3 days after I take my shot, I feel vaguely like I'm going through withdrawal like sweaty, a little manic, jittery, rapid temperature shifts, and just like my whole body feels of