Hair loss is one of it's side effects

I've experienced hair loss but not sure if it is from Tecfidera or flares. I've read in support groups hair loss was common with Tecfidera.

When I start to take Aubagio, my hair start to thin out I was losing hair every day.

I've noticed hair loss and I'm using Copaxone. I've been trying to find info but not sure if it's the medication or MS itself - or genetics! :)

Once when I had solumedrol via IV 2 months in a row, half my hair fell out. It grew back though :)