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Re: sts66 post# 213469

Tuesday, 09/10/2019 3:47:05 PM

Tuesday, September 10, 2019 3:47:05 PM

Post# of 426172
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.

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