date:Apr 28, 2012
to heart attack.
TheFDA has received 42 adverse event reports on products containing DMAA, it said:While the complaints do not establish that DMAA was the cause of the incidents, some of the reports have included cardiac disorders, nervous system disorders, psychiatric disorders, and death.
It added:There is no information demonstrating that DMAA was lawfully marketed as a dietary ingredients in the US before October 15th 1994, nor is there any information demonstrating that it has been present