CYCLOSPORINE vs Etanercept

Is IV cyclosporine 3 mg/kg, for example, the same as PO cyclosporine 3 mg/kg? It seems like many providers treat it this way, 1:1 conversion but some sources online say 3:1? Could you help explain the difference in practice vs. online sources? Thank you!

Our department hired a new NP recently and is shadowing in clinic. She was asking about cyclosporine and I made an off the cuff remark that she shouldn't be too worried because she shouldn't be prescribing it anyway (after educating her about the labs to follow, doses etc.). When she leaves she says

Yesterday I was at work, sitting at my desk looking at my computer screen. I started to notice black splotches appearing in my vision, similar to what I have seen in the past when I have stood up too fast. I have never experienced this sitting down before but I wasn't alarmed and figured I'd wait it

this is about my aunt (female, late 50s, black, high BMI) just now. her reading came down to 195/97 on the arm cuff machine we have at home but im really worried. she’s already on BP meds (and a plethora of other meds). she started a regimen of cyclosporine for membranous nephropathy(sp?) and protei

I apologize for the strained wording. I tried to Google this but I couldn't figure out the right search terms. In the US, generally health insurance will not pay for medications prescribed for non-FDA-approved/"off-label" uses, and/or for compounded medications. It is completely legal to prescribe o

Age: 64 Sex: F Primary medical issue: Mother was diagnosed with AML FLT3 TKD in September of 2021 * Current medication: Mag, Calcium+Vit D, Acyclovir * Current Care: Every other week visit with either local oncologist or nurse practitioner, every couple months telemedicine with Fred Hutch clinic

* **Age**: 26 * **Sex**: Male * **Height**: 6'2" * **Weight**: \~145lbs * **Race**: Caucasian * **Duration of complaint:** 2 years for red cell aplasia, 8 years for CVID * **Location** (Geographic and on body):Denver, CO * **Any existing relevant medical issues (if any):** Red Cell Aplasia, CVID, Hx

Hello all, I'm looking for advice/insight into my medical history. I'm a 38 year-old man, diagnosed with Autoimmune Hemolytic in Jan 2018. Since then I've relapsed twice, with the least severe episode being the last in OCT 2020. The first and last episodes were treated with oral corticosteroids, an

This is too much isn't it? I need advice!  I'm unsure which of my doctors can help me and hoping someone here can tell me which doctor to talk to, what questions to ask, and what I might be overlooking or misinterpreting. I live in East Texas. My husband has great health insurance, but we have v

Hey there! I’m coming up on 30 years living with RA. I was diagnosed as a young woman - only 22 years old! I was originally diagnosed seronegative RA, but am now seropositive. I’ve been on biologics over 25 years. I’ve managed to lead a full life after diagnosis: corporate career, two kids, world tr

hi guys, I recovered from long Covid, it started beginning 2022 for me and I relapsed many times, because any time I recover I’d get Covid again and bam another 3 months in bed. I’ll probably get it again, if I get Covid again. But I really pray and take all precautions to not get it. I know it’s di

​ [Stockhead Image - https:\/\/stockhead.com.au\/health\/incannex-has-positive-pre-ind-meeting-with-us-fda-on-ihl-675a-for-treatment-of-rheumatoid-arthritis\/](https://preview.redd.it/1h5zxr69o6ib1.png?width=2338&format=png&auto=webp&s=91dc29b8a14eea7ea69d1cf39265915cf2107e9d)

Hi everyone, I'm writing on behalf of my partner, because we’re both overwhelmed and could really use some advice and support. After nearly **8 years of pain and being misdiagnosed**, he was finally diagnosed with **Ankylosing Spondylitis (AS)**. For years, doctors said it was just stress, posture,

Edit: some folks brought up the very good point that you need to balance effects of any treatment against the effects of doing nothing. I was only focusing on the side effects of TNFi bc that's what I received a bunch of good (published) shareable info from my doc on, but we have had previous conver

I have been doing a lot of AI deep searches to find a way to reduce PD progression by using various supplements. Below is the extract of the findings. I suspect that for people at the early stages of PD might benefit from the effects and potentially slow down PD progression. If we have enough peo

I just switched insurances (new job), and my new insurance won't cover Enbrel for psoriatic arthritis, preferring one of 3 other TNF blockers. I've been on Enbrel for the last 5 years, and would really rather not switch away from something that's working so well, especially since I work in healthcar