Hi guys seen theres new drug aubagio available to rrms is anyone on it? Any info cant find anything on it now Xx
Loads on Internet google it !
It was only approved last week in the UK, so I don’t think you’re going to find a whole bunch of people on it yet. And if there were, a week is a bit soon for them to tell us how it’s going. Unless somebody had an absolutely awful reaction within a day or two of starting, they’re probably still playing wait-and-see.
There is a news article about it right at the top of the “related content” panel, at the top right hand side of this forum.
Tina
Thank you tina That was only article I could find was worth asking though Xx
I thought it wasn’t being prescribed until April? Anyway, if it’s anything like Gilenya, I would rather have the injections!
Aubagio | National Multiple Sclerosis Society Ooh I don’t like the sound of some of those side effects. I was told I might be offered this or Copaxone, but I don’t fancy injecting either (I had problems with injection sites from heparin injections from a DVT).
It was released this month from what I can find on here. Im currently on copaxone now been on it since last march gotta say not once had problem with injection sites Xx
Says from April here: http://www.mssociety.org.uk/ms-news/2013/12/nice-confirms-new-oral-treatment-ms-nhs
Not heard much about it I’m on rebif tho and there’s complications 5 people from where I am Aka the west of Scotland have had side effects and one death so changing to avonex does anyone no if it’s any good or works any probs etc ??