CYCLOSPORINE OPHTHALMIC SOLUTION vs EVEROLIMUS

* 37/F * Health issues: Hypothyroidism, ocular rosacea with flairs of scleritis and other inflammatory issues, vitamin D deficiency, depression, anxiety, occasional problems with candida * Current medications: Synthroid, Celexa, Klonopin, 2% Miconazole cream, prednisolone ophthalmic solution as ne

Hello I live in Japan and have 27 years old I am 170cm tall and 60kg, from three days ago I got an infection in my left eye, which I presumed it was pink eye. Later my right eye got involved and got a low fever. I went to the medic and gave me two kind of eye drops (GATIFLO OPHTHALMIC SOLUTION 0.3%)

Hi. 44 yrs old female, 190lbs, non smoker, wears glasses, no contacts. No prior history of medical issues, no family history of autoimmune, I have had migraines in the past, but nothing diagnosed. Currently not on any daily medication, but will use NSAIDs for pain and ketorolac 0.5% ophthalmic solut

***Edit: For anyone who cares, the neuro diagnosed it as "ophthalmic migraines" and basically said there's nothing to be done to prevent it, and it's not connected to his glaucoma. He just has to ride it out and they may or may not end. Hopefully this post helps someone else looking into ophthalmic

28 YO Male, White, 5'7", 165 pounds. I am sorry for the length of this post but I genuinely feel that all this info is or can be relevant. I have been to different specialists, but feel that everyone is looking at my issues in a vacuum of their specialty. I am desperate for a solution. Thank you for

EDIT; NOPAIN act-- not paint... Any hospitals or surgical centers plan on making any changes surround this? Apparently a separate payment will become available 1/1/25 for non opioid alternatives post op. Drugs are the following that will get average sales price + 6%. EXPAREL^(®7) (bupivacaine liposo

Hi guys, I work at a refill center in Texas and need help regarding bioequivalent substitutions: 1) The doctor asked for Timoptic-XE but the original pharmacy filled it with timolol ophthalmic solution. I looked at the orange book and it says that solution/drops is AT1. Does that mean it's an ok sub

I share this for the benefit of others looking for hope in treatment for metastatic RCC. As we know, everyone's case is different and my experience is my own. I (48,M) am about 22 months following diagnosis with RCC, 21 months post radical nephrectomy (left). I was diagnosed with metastatic lesions

´´Long COVID is frequently discussed in this subreddit so I thought this is probably a good place with knowledgable people to ask this question. I recently stumbled on this article: [My Long.COVID Prevention Protocol.](https://desmolysium.com/covid/) The author notes that his friend who has long CO

I tried rapamycin after reading [this article](https://www.healthrising.org/blog/2022/07/06/apamycin-resurgence-doctor-chronic-fatigue-syndrome/) on health rising blog, but it made no difference to my symptoms. Many people believe CFS involves neuro-inflammation so I decided to try the closely rela

Hi, I just found an article and the author claims to have been on rapamycin for 4.5 years. This is probably the longest time I have heard of anyone being on rapamycin in an uninterrupted fashio. It is highly informative so I recommend to check it out: [**My Experience With Rapamycin**](https://desmo

I am 7 weeks post liver transplant. My team asked me to join a clinical study which would take me off Tarc and replace it with a medication called Everolimus. This medication is supposedly just as effective as Tarc but less stressful on the kidneys. Does anyone have any experience with this medicati

I graduated in March as an LVN. I started my new and first nursing job about a month ago. I work at a SNF… I love my job so much and enjoy seeing my patients. I would go deeper into everything, i’ll keep it short. I don’t think i was properly trained, was taught a lot of short cuts and tricks for me

Got a message from my transplant hospital today informing me that I’ll be covered through June but no guarantees after that. I didn’t even know they were in negotiations! My meds will be available through June but no idea what July will look like. I can’t afford my meds without insurance. I could a

I work at a kinda big pharma plant, and deal with some unpleasant stuff. Our latest batches are mostly bound for the USA, and a minor amount is for other markets. If you happen to use, or have used some of these medications, i'd like to hear if they really help. These aren't all the meds we make, ju