Experiences with

Entyvio

I am overseas am having trouble sourcing Entyvio I am late for my dose by 12 days a bit concerned about the delay. Has anyone been in this situation before?

I have ulcerative colitis with inflammation of the cecum that may be due to lupus or meds. Not really sure. I’m advised to take something similar to one of the drugs questioned to reduce inflammation. I have ckd 3b and don’t want to make it worse. Trying to determine which is better.

I had a bad side effect with infliximab so now have to decide whether to continue with Entyvio or sterlara? I have read up but anyone got any advice?

bad effects with infliximab so suggested to go to entyvio so read up on that and now it’s humia?? I’ve read about it and still don’t know why this one would me? I’m UK so it’s not insurance? How do they make decisions.

Now doc recommends Entyvio infusion without treating my latent TB a risk which both myself n doc discussed b4.

It went back to >6000 again and he is going to start Entyvio as soon as we get approval from the insurance. What I actually want to know is if there is anyone who had Calprotectin levels this high. My son has been to 3 doctors - none of them can explain this ridiculous high result.

IL-12/23 or IL-23 inhibitors include such therapies as Stelara, Tremfya, and Skyrizi; integrin inhibitors include Entyvio. The other good news was that combining therapies, such as taking methotrexate along with a TNF inhibitor, did not have an additional reduction on antibody levels.

I've been on Remicade, Humira, Entyvio, and Enbrel and those are just the biologics I've failed. There are endless other failed meds, and I am so very very tired. It has been a long, hard road. I need this to work. I want to try Cimzia again just to make sure it wasn't a one time event.

Entyvio is rather new to pediatric patients so no one here really knows how long it will take to work, if it is going to. Can anyone tell me how long it took to see results from Entyvio infusions?? Thanks.

Can anyone tell me how long it took to see results from Entyvio/vedolimumab infusions?? Thanks.

The doctors want me to start with Entyvio... are there natural remedies to deal with Crohn’s.

I am on medication and am currently taking Entyvio, which is gut specific and is keeping gut symptoms at bay, and Imuran and Methotrexate (which I'm currently working up to a higher dose).

I'm currently on Entyvio which is gut specific and has my GI symptoms in check, but my extra-intestinal symptoms are flaring including arthritis and iritis. I've been on Imuran with Enytvio, but that hasn't gotten rid of my flare, so my rheumatologist added Methotrexate.

Hi newby here has any one been on entyvio I’ve been on it for 5mths get bad headache stiff joints and itching had Colits for 12 yrs infusion every 8 weeks 12yrs

I am also on entyvio infusion every 8 was if that makes any difference. Thanks I'm at a loss and don't want to lose any ground I've made 😔

I am on entyvio infusions it is working for me thanks to Dr .Navaeethan @ Florida hospital in Orlando Florida

I begin entyvio next month and it is my last hope before surgery becomes a reality. Currently I am having to have iv fluids once or twice a week due to the dehydration and my pulse rate jumping high.

I am struggling a lot with my crohns I started entyvio treatments 2 weeks ago and I'm on other meds my white blood count is elevated and has been for awhile now my liver levels r elevated also I'm so tired of being tired and depressed I just want to get better for my family and kids please help any advise

My specialist is not pleased with my choice not to be on another biologic like Humara or Entyvio but I am convinced they are poison! My last fecal protectin test showed high levels of inflammation but I am working on lowering that with diet. I would be happy to offer my help to anyone!