Apremilast vs USTEKINUMAB

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

Even though several of these medications are manufactured in the USA, it doesn't mean it's cheaper in the USA. "Socialised healthcare" negotiates in a free market outside the USA. No wonder travel insurance costs a fortune in USA. Detailed story..... https://www.msn.com/en-au/health/other/doctors-

Welcome back to this week's newsflash 1. Surgery for UC can be a major life change, but it is often a necessary step when medications fail. Understanding the adjustments to diet and daily life afterward is crucial for recovery and long-term well-being. This guide explores what patients can expect re

#The Effectiveness of Medications for Ulcerative Colitis *This post was last revised September 19, 2019.* Here I have compiled data on the effectiveness of medications used to treat ulcerative colitis, as compared to placebos or to other medications. ###Risk Ratios (RRs) All values here are shown as

Since eternacept started to wear off over the years my docs gave me the choice to switch to Ustekinumab. The 3 months injection rhythm sounds pretty unreal when coming from 3-day-interval Eternacept jabs, but well.. you could call it progress in medical science. I am now 3 weeks in after my first do

I wanted to follow-up on a previous post I made regarding starting Stelara. https://old.reddit.com/r/Psoriasis/comments/yjhr6z/plaque_psoriasis_after_a_covid_vaccine/ I have now be on Stelara for 7 months and it has nearly cleared my Psoriasis. I stopped applying Clobetasol some months ago and each

I’ve been on biologics for about a year now, i started in December 2024. About 45ml shot of Ustekinumab every 3 months as prescribed by my dermatologist. Problem is, it is losing its efficacy. Since August, every time it clears up about 70%, the same thing happens, it comes back worse even with topi

Phase 3 trials to commence. Possibly another biological option. http://www.medscape.com/viewarticle/878838