COVID-19 vaccines have enhanced reporting requirements for vaccine safety database, so death reports cannot be simply compared to other vaccines
Manufacturers and healthcare providers must report all serious adverse events that occur after COVID-19 vaccination, regardless of whether they think the vaccine was the cause. This is mandatory under the Emergency Use Authorization that the FDA issued for the COVID-19 vaccines. In 2021 and 2022, clinicians administered over 600 million vaccines, an unprecedented number under such authorization, leading to a spike in deaths reported to VAERS. Taken together, this indicates that the spike is due to an increased reporting rate and not a genuine increase in deaths.