I don't think we have anyone here that is on Rinvog. There are quite a few on it in the UC forum & they are very happy with their response. In your prior posts you say you have UC, has this changed? Try to keep in mind with any drug, there is always a potential for an unwanted side effects.
Has your dr prescribed this for you? What medications have you tried in the past?
I was originally diagnosed with UC in when I was 13 years old back in 2003. It was changed to Crohn’s disease when I developed fistulas, so I officially have Crohn’s disease.
Thanks for your responses. It seems to be safer but I just wanted some input. I’ll ask in the UC forum. My doctor prescribed it after stelara stopped working after a few years and had no response to Skyrizi.