ADALIMUMAB-AQVH vs ADALIMUMAB-BWWD

$995 for a carton of 2 auto injectors vs Humira's $6922, good news for the patients. We can hope for more price reductions as the market is expecting at least 11 Humira biosimilars to be released.

This is my first time posting in this community, although I’ve lurked ever since I was diagnosed a little over a month ago. About 3 years ago I woke up with insane elbow pain out of nowhere. That was the only joint that hurt, but it was super intense considering when I went to bed the night before

My employer switched insurance companies at the beginning of the year. I am now on WPS and use SmithRx and Costco Speciality Pharmacy to get my meds delivered to my house each month. I am on Zeposia and have been since January 2023 without any relapses and no side effects. I got a letter from Smith

I have Crohn's disease and I'm trying to narrow down what health plan I wish to go with. I used to be on Humira, but my old insurance in the private sector moved me to a biosimilar named Yusimry. Based on my research, none of the Federal plans cover or supply this drug, so I'm willing to move to a b

Hey chat, has anyone switched to Yusimry from Humira? Or experiences with other biosimilars? I’m considering making the jump due to insurance reasons so plz lmk your experiences with Yusimry or other products.

Hi, I'm totally new to this subreddit, so please bear with me! I was diagnosed with Juvenile Idiopathic Arthritis (However, it's Rheumatoid in my jaw) in October of 2021. I've been on Humira for 4 year now since then and it has worked pretty well (besides irritation at my injection site, handled wit

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