FDA Announces 2 Deaths of Pfizer Vaccine Trial Participants from “Serious Adverse Events” (Updated – Withdrawn)
By GMI Reporter
Note: Our report on 2 deaths within the Pfizer Covid vaccine trial reported in the FDA guidance document released on Dec. 8th, 2020, has been temporarily withdrawn for editorial review by Greemedinfo.com staff. This decision was made in response to the sudden removal by the Jerusalem Post of their article from Dec. 8th titled, “FDA announces deaths of two Pfizer vaccine trial participants,” which can be found in web archived format here: https://web.archive.org/web/20201208142015/www.jpost.com/breaking-news/two-individuals-die-from-pfizer-vaccine-651488
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.Â
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.”
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:
2 Calls To Action
1) There is growing concern among the public and health professionals, alike, over the uncertain safety of COVID-19 vaccines. Given the FDA’s clear acknowledgment that death, and other life-threatening conditions, are known possible adverse outcomes of the COVID-19 vaccine, it is absolutely necessary for vaccination with them to be voluntary and not mandatory. Informed consent requires that you know the real risks, and make a clear and conscious choice to consent to the intervention beforehand. Join us at Stand for Health Freedom and ACT NOW: Tell your governor and local legislators that COVID-19 vaccines must be voluntary!
2) There are two upcoming FDA advisory committee deadlines coming up for public comments ton the COVID-19 vaccines on Dec 10th and Dec. 17th. These will be livestreamed. Attend and make a comment!
Vaccines and Related Biological Products Advisory Committee December 10, 2020 Meeting Announcement
Vaccines and Related Biological Products Advisory Committee December 17, 2020 Meeting Announcement
Disclaimer: This article is not intended to provide medical advice, diagnosis or treatment. Views expressed here do not necessarily reflect those of GreenMedInfo or its staff.
This article is copyrighted by GreenMedInfo LLC, 2020
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