Electronic Submission of Adverse Event Reports to FDA FAERS

Taiwan Draft Guidance on Adverse Event Reporting

How the Vaccine Adverse Event Reporting System (VAERS) works

Dr. Rose’s research involves descriptive analysis of data using the US Vaccine Adverse Event Reporting System (VAERS). The COVID-19 injectable products were rushed to market via Emergency Use Authorization (EUA) and corners were cut in pre-clinical and clinical trials (only healthy people within a certain age requirement were able to participate in the phase 3 trials, placebo participants were unblinded and injected with the produce, thus losing a comparative group). The COVID-19 injectable prod

54 reactions · 39 shares | Dr. Rose’s research involves descriptive...