FDA Announces 2 Deaths Of Pfizer Vaccine Trial Participants From “Serious Adverse Events” By GMI Reporter for Natural Blaze
Following only a day after our report that the FDA knows about and is preparing for COVID-19 vaccine adverse outcomes which include deaths, a newly released document on the FDA website shows that 2 participants died as a result of “serious adverse events” from the experimental Covid vaccine.
In an FDA Briefing Document released on December 8th titled, “Vaccines and Related Biological Products Advisory Committee Meeting December 10, 2020,” clinical trial results from the Pfizer/BioNTech COVID-19 vaccine reveal two study participants died from what were classified as “Serious Adverse Events.” On page 41 of the document two vaccine recipients classified as “>55 years of age” died: “[O]ne experienced a cardiac arrest 62 days after vaccination #2 and died 3 days later, and the other died from arteriosclerosis 3 days after vaccination #1.”
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As reported in The Jerusalem Post:
The FDA announced on Tuesday that two trial participants have died after receiving the Pfizer coronavirus vaccine, according to Reuters. According to Walla, one of the deceased individuals was immunocompromised.
The documents were released ahead of a upcoming meeting on Thursday of outside experts who will debate whether emergency authorization for the vaccine should be granted.
The FDA also said on Tuesday that the data they’re presented with is in line with emergency use authorization, raising hopes for Thursday.
According to Maariv, the sister publication of The Jerusalem Post, the FDA announced on Tuesday that there currently is not enough research to guarantee the vaccine’s safety for immunocompromised groups, pregnant women and children.
This report follows closely on the heels of the discovery that the FDA’s own public discussion and documents about the COVID-19 vaccines acknowledge that deaths and 21 other conditions, many of which are life-threatening, may result as adverse outcomes from these vaccines. Read more about this developing story here:
