Evidence That Demands An Explanation

This is a list of potential “Contraindication” they knew about, prior to rolling out the Covid-19 serums, since the date is prior to the roll out of any of them. Most are the exact diseases we are seeing being reported on VAERS, that are killing and injuring many people. The CDC wants us to believe these deaths and injuries are coincidences.

From the FDA Power Point Presentation titled:  

Vaccines and Related Biological Products Advisory

Committee October 22, 2020 Meeting Presentation

Page 16 Titled and duplicated as exactly  as possible:   

FDA Safety Surveillance of COVID-19 Vaccines : DRAFT Working list of possible adverse event outcomes ***Subject to change***

  • Guillain-Barré syndrome
  • Acute disseminated encephalomyelitis
  • Transverse myelitis
  • Encephalitis/myelitis/encephalomyelitis/ meningoencephalitis/meningitis/ encepholapathy
  • Convulsions/seizures
  • Stroke
  • Narcolepsy and cataplexy
  • Anaphylaxis
  • Acute myocardial infarction
  • Myocarditis/pericarditis
  • Deaths
  • Pregnancy and birth outcomes
  • Other acute demyelinating diseases
  • Non-anaphylactic allergic reactions
  • Thrombocytopenia
  • Disseminated intravascular coagulation
  • Venous thromboembolism
  • Arthritis and arthralgia/joint pain
  • Kawasaki disease
  • Multisystem Inflammatory Syndrome in Children
  • Vaccine enhanced disease
  • Autoimmune disease

16

Full Power Point Presentation: https://www.fda.gov/media/143557/download 

As you can see this list was created before the vaccines were even approved, with the 1st the Pfizer/BioNTech vaccine given Emergency Use Authorization (EUA) on December 11, 2020, for the Modera vaccine a week later and the Jenssen EUA was granted in late February of 2021.

Source: https://www.fda.gov/news-events/press-announcements/fda-takes-key-action-fight-against-covid-19-issuing-emergency-use-authorization-first-covid-19

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