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Re: Biobillionair post# 213472

Tuesday, 09/10/2019 6:30:13 PM

Tuesday, September 10, 2019 6:30:13 PM

Post# of 425892

On 9-29 the FDA will have taken an action that directly harms 20% of all new Vascepa prescribed patients. 1 out of every 6 of those patients will have an event waiting for the FDA...

Any delay beyond 9-28 is actionable regulatory malpractice, the FDA is not chartered to IGNORE standard of care.

BB



I am not sure where you got those numbers from...
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