Former FDA official: FDA negligent in not investigating myocarditis cases

The following article was written by David Gortler, a senior policy advisor at The Heartland Institute, and is the first pharmacist to be appointed to serve on the US Food and Drug Administration (FDA) Senior Executive Leadership Team.[1]https://former-fda.com/about-fda/fda-organization/david-gortler/ It was published by The Federalist last February 10, 2022.

Here are the most important points raised by Gortler in this article:

  • The FDA knew from the very beginning that the COVID vaccines were linked to “serious heart trouble” in its recipient.
  • Several FDA safety epidemiologists have stated during official FDA presentations that it only takes a single well documented adverse event to justify a safety signal investigation and to warn the American public.
  • The long list of reports of heart attacks, myocarditis, and pericarditis in the US should have spurred the FDA into full investigation mode.
  • The US Center for Disease Control and Prevention (CDC) Vaccine Safety Datalink indicates an excess risk of myocarditis and pericarditis in recipients following the Pfizer and Moderna vaccines.

Editor’s Note: This article is valuable because Gortler knows what he is talking about. As a well-respected drug safety expert and a member of a high-level advisory board at the FDA, he knows that there is more than one way for the FDA to detect the safety signals from the COVID vaccines.

It is clear from Gortler’s discussion that the FDA is committing gross negligence for allowing the COVID vaccines to continue to be rolled out despite the massive heart health damage it is causing.

Now we must ask: Why won’t the US government pause the COVID jabs from the market? Why are they attempting to vaccinate the very young who stand nothing to gain from getting the shot?

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