Anyone taking Entyvio

[tamRN]

I have been on Humira since late August with little improvement of my UC. Seen my gastro yest and she called back today wanting me to start Entyvio in a couple of weeks being I just took my Humira this morning. Seems like I cant stay off prednisone. Im currently taking, Uceris, sulfasalazine, humira, canasa supp.

Just wondering if anyone has started this infusion and what side effects u migh have had or if it worked for u.

 

[Fernando1]

Have had two doses of Entyvio, no side effects at all (I hear that people get headaches and feel fatigued), not for me, nothing at all.

I hear that it takes 14 weeks to begin to see changes.

See Entyvio thread for hundreds of posts on Entyvio experiences.