Anyone using Adalimumab-Adbm (Cyltezo) for Psoriasis? Share your experiences!

I've been on Cyltezo for a year now, and it's been a godsend. My psoriasis is under control, and the side effects have been minimal. I get a bit of a headache sometimes, but nothing I can't handle. I've had a UTI, but I'm not sure if it was due to the medication because they are common. Just keep an eye on any unusual symptoms and talk to your doctor.

I've been on Cyltezo for a few months now, and I've had some side effects, but overall, it's been worth it. I've had some skin irritation and redness at the injection site, but nothing too bad. I've also had some headaches and fatigue, but again, it's not that bad. I've also had a UTI, but it was easily treated. Just make sure you keep track of any weird symptoms and talk to your doctor about it.

I just started Cyltezo a few months ago, and I've had some interesting side effects. I noticed some skin lumps and redness at the injection site, and there's also some pain at the injection site occasionally. I got a lot of information from a nurse during my trial run. I spoke to my doctor and she said that is common. Non-steroidal anti-inflammatory drugs should help with any pain. Just wanted to share my experience, hope it helps!

Jeez, it's scary reading about all the potential side effects. I've had psoriasis for years and I'm seriously considering Cyltezo, but these lists are not reassuring. Anyone had any really bad experiences?

I just wanted to mention, if you're nervous about giving yourself injections, it's totally normal. It took me a few tries to get used to it, but now it's just part of my routine. Just remember to use a different spot each time. Oh, and take it easy on the alcohol after you inject. Don't drink too much.

I've had psoriasis for 10 years and after many years of treatments that didn't work it seems like Cyltezo is finally starting to manage my disease. I have had a few allergic reactions but they were mild. I do get some UTs though. I guess that's just my body's response. My doctor says it's not uncommon. It's worth it to see my skin clearing up. Think of the alternative: years of psoriasis treatments that make you miserable. At least this one is letting me live relatively normally.

I've been on Cyltezo for about a year and it's been a nightmare. I've had some really bad side effects, including severe headaches and joint pain. I'm not sure if it's worth it anymore. Maybe I should talk to my doctor about switching medications. My psoriasis is improving, but I'm not sure if it's worth the side effects.