Apremilast vs BRODALUMAB

This is a 38-year-old female with multiple medical problems including psoriasis and psoriatic arthritis for which she receives secukinumab, apremilast, and leflunomide. She is admitted to the hospital on November 16 for progressive dyspnea and generalized body pain. She has chronic sinus congestio

What’s going on with me is kind of a question mark so I’m thinking of throwing it out to the internet for some ideas. I know my doctors are doing their best and I feel taken care of but not getting any real answers and they’re really overworked with the pandemic. It’s not instead of, because I am be

I'm 17M Asian 5'11 weigh around 190 lbs. I was diagnosed with plaque psoriasis 2 weeks ago. My arms were already getting better and barely any flare-ups were happening as I was using the meds my doctor prescribed which were oral apremilast/otezla 30mg a day and topical 0.5% bethamethasone ointment,

I am a radiologist. I just received antirabies treatment few hours ago. I wonder if topical clobetasol has any effect on efficacy of rabies treatment. I take apremilast 10 mg for psoriasis O.D. Other than that, im taking Vitamin D shots (60000 IU weekly) Non-alcoholic Non-smoker

* **Age:** 24 * **Sex:** M * **Height/Weight:** 170cm / 75 kg * **Race:** Indian (Honestly, I don't know.) * **Primary Complaint:** Questioning treatment plan for Alopecia Areata * **Duration:** 3 years * **Any existing medical issues:** Hypertension and Ulcerative Colitis * **Current medications an

Italia, uomo, 31 anni, 60 kg, non fumatore. Sportivo, da sempre alimentazione sana. Ciao a tutti. Da inizio 2023 ho costantemente ulcere orali, macchie rosse e piccoli rigonfiamenti in bocca. All’inizio erano numerose e molto dolorose; oggi la situazione è più “leggera” ma persiste: di solito

Earlier today I was browsing Reddit and stumbled [upon a post](http://www.reddit.com/r/AskReddit/comments/33ej71/disabled_people_of_reddit_what_is_something_we_do/cqkbwu7) It made me remember all I vowed to do if I ever managed rid myself of psoriasis. To this date I’ve not yet shared a whole lot

I'm currenlty engaged in a clinical trail for a new drug called "Brodalumab", am considering doing an AMA. Is there enough interest in this to warrant the AMA? My P had taken over 80-90% of my body and is now well under 5%. It has been a life changing experience and I want to tell others of the hope

Hello folks, Apologies if this is against the rules despite my reading them, I wanted to ask if folks have any experience with Leflunomide with treating psoriatic arthritis. I'm already on Brodalumab which has completely reversed the skin side but now at 35/36 I've started getting awful joint pains

Hello everyone, I've been dealing with psoriasis for about 9 years. I've tried Methotrexate and also Accutane. The latter helped significantly at first, but eventually stopped working. Now I'm supposed to start a medication called Kyntheum (active ingredient: Brodalumab). It's a biologic. Has anyon

Herein we explain how our novel data mining strategies for RNA-Seq datasets lead to new insights into the pathophysiology of psoraisis, an immune-mediated disease involving the skin. This story can also be found in [our recently published manuscript in JCI Insight.](https://insight.jci.org/articles/

I've been desperately looking into the 'cures,' making headway with recent science. As I've been going through an especially treacherous winter flare. It seems like stem cell therapies have made some profound headway in permanent remission of this disease, but unfortunately they are not legal treatm

Like the title says, I was supposed to start on Taltz but my doctor presumed that Siliq or Brodalumab would be best for me, He asked if I had any depression etc, I said I was never diagnosed but I do experience spells of depression as do anyone, I'm wondering if anyone here uses Siliq/Brodalumab an