User Reviews for Mayzent oral

I was diagnosed in 2009 with RRMS and just before starting Mayzent, it became SPMS. I’ve been on copaxone, tysabri, and tecfidera in the past but stopped because of side effects, effectiveness. I’ve been on Mayzent since 2020 and I’ve been really happy with this medication. It’s not a pill that I take and have to follow up with antinausea meds like tecfidera but just a tiny pill that I take every evening before bed. I haven’t noticed any differences since starting besides having less episodes. I can’t recommend it enough. For the first time in my life i had an mri with no changes on it from the last one. I still have issues that i started with but beyond that i feel somewhat normal.Read More Read Less

My experience on Mayzent, been on it maybe ?? 2 years that's how bad it affected my memory, at first I did gain weight then I lost 60 lbs in 6 months, walking slowly deteriorated, pain in arms, legs especially at night, insomnia,vision problems, diarrhea, mental health it it all slowly worsened so I didn't even realize what was causing it constant UTI's, breathing difficulties, osteoporosis, severe migraines, and so much more been trying to tell my doctor even my daughter Dr. just said (of course your mother had MS for over 30 years) but I was doing better before Mayzent now I just feel like I'm dying everydayRead More Read Less

I declined, perhaps coincidentally— from almost the moment I started taking Mayzent. After 6 months I got my first ever UTI. But all my labs were low but stayed in range