That is one of the questions the FDA has to answer on the 7th.
It is not something I'd want to personally find out about. But then if I was given an AD diagnosis and was starting to lose ground at fast rate I might reconsider. After all, at that point there isn't a whole lot to lose.
bb and T, has Biogen detailed the extent brain bleeds were associated with the higher doses or was it uniform over the entire patient population? I did not see anything regarding the delineation of this SAE.
TIA
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