Anyone on Entyvio every 6 weeks?

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Date Joined Aug 2017
Total Posts : 88
   Posted 1/12/2018 12:19 PM (GMT -6)   
I've been on Entyvio every 8 weeks since the summer. It def has helped, but i would say only to about 65-70%, which is much better than the 0% I was getting from Humira & Azathroprine.

My new doctor isn't happy with the entyvio at 8 weeks but doesnt necessarily want me to come off of it because we have gotten a reaction when no other medication has gotten me to this point so we decided to bump me up to every 6 weeks.

I was curious if anyone has been on Entyvio at 8 weeks before moving up to 6 weeks? Curious to see if your symptoms got better or anything like that. I'm hopeful because I like entyvio, havent gotten side effects from it like 6mp and others, so I'm hopeful this is the dosage that can get me to remission.

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Date Joined Aug 2012
Total Posts : 11806
   Posted 1/12/2018 1:23 PM (GMT -6)   
Are you only on entyvio at this point? I ask as combination-therapy is often produces the best results for us. Since you had a reaction with 6mp, had you considered adding oral and rectal-route mesalamine to the entyvio? Might give you the extra boost you need.
Moderator Ulcerative Colitis
, 39, UC Proctosigmoiditis
Rx: Remicade @5mgs/kg/6wks; daily 75mgs 6MP, 4.8g generic-Lialda, and rowasa

A semi-finalist in the Olympic 15-meter bathroom-sprint. Aimed for the gold but just ended up getting brown...

Regular Member

Date Joined Jul 2015
Total Posts : 79
   Posted 1/13/2018 7:25 AM (GMT -6)   
Completely agree with IPoop, hit it from every angle.
Pancolitis DX:
Fall 2007

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