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Congress members demand FDA Investigate COVID-19 Vaccine Injuries – Sept 2022

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Congress Members Send Demand Letter to FDA Commissioner: Investigate COVID-19 Vaccine Injuries Now
CDC Has 4 Days to Release Data on COVID Vaccine Injuries Collected via V-safe App, Court Rules - Sept 26
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Congress Members Send Demand Letter to FDA Commissioner: Investigate COVID-19 Vaccine Injuries Now

TrialSiteNewsn Sept 25
"VAERS has received over 1.4 million reports of adverse events following the administration of the vaccine."

Anaphylaxis, which is a severe and potentially life-threatening allergic reaction, from the first Pfizer/BioNTech vaccinations
Thrombosis with thrombocytopenia syndrome (TTS) after Johnson & Johnson’s Janssen Biotech COVID-19 vaccination
Myocarditis (inflammation of heart muscle) or pericarditis (inflammation of the outer lining of the heart) after COVID-19 vaccination
Guillain-Barré syndrome (GBS) after Johnson & Johnson’s Janssen Biotech COVID-19 vaccination
VAERS has received over 30,700 reports of death among recipients of the COVID-19 vaccine, although no causal link between the vaccine and death has been determined

CDC Has 4 Days to Release Data on COVID Vaccine Injuries Collected via V-safe App, Court Rules - Sept 26

Childrens Health Defense

See related in VitaminDWiki

Congress members demand FDA Investigate COVID-19 Vaccine Injuries – Sept 2022

1026 visitors, last modified 26 Sep, 2022,

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- CDC not look at VAERS COVID vaccine data until 2022, still has not reported on it - Jan 2023 400 doctors, scientists declare “international medical crisis” due to COVID-19 vaccinations - Sept 2022

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