I am currently on Pradaxa, (been lnearly 2 weeks now) and it seems to be working fairly well for me so far. My hands usually cold and very red with white fingertips are feeling very warm and toasty latey and slowly the red is fading!
And I am feeling well. That is the most important thing. I haven't noticed any negative side effects at all.
Is anyone participating in the clinical trials on APS patients in the UK?