A Report on the U.S. Vaccine Adverse Events Reporting System (VAERS) of the COVID-19 Messenger Ribonucleic Acid (mRNA) Biologicals

“Abstract: Following the global roll-out and administration of the Pfizer/BioNTech (BNT1 62b2) and Moderna (mRNA-1 273) COVID-1 9 vaccines1 on December 17, 2020 in the United States, and of the Janssen COVID-19 Vaccine PF (produced by Johnson & Johnson) on April 1st, 2021, tens of thousands of individuals have reported adverse events (AEs) using the Vaccine Adverse Events Reports System (VAERS). This work summarizes this data to date and serves as information for the public and a reminder of the relevance of any adverse events, including deaths that occur as a direct result of biologicals as prophylactic treatments. This is especially relevant in the context of technologically novel treatments in the experimental phase of development. Analysis suggests that the vaccines are likely the cause of reported deaths, spontaneous abortions, anaphylactic reactions and cardiovascular, neurological and immunological AEs… BBB Conclusion: … [D]ue to both the problems of under-reporting and the lag in report processing, this analysis reveals a strong signal from the VAERS data that the risk of suffering an SAE [Severe Adverse Event] following injection is significant and that the overall risk signal is high.”