CDC VAERS Adverse Events, Analyzing The VAERS Reports With Researcher WelcomeTheEagle88

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This could be the problem. From ICAN: Informed Consent Action Network:
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ICAN, through its attorneys, has written to HHS Acting Secretary Norris Cochran and Rochelle Walensky, the new Director of the Centers for Disease Control and Prevention, to demand that all adverse events following COVID-19 vaccination which are reported to the CDC’s new V-safe tool also be automatically reported to the Vaccine Adverse Events Reporting System (VAERS).
As discussed in prior legal updates, the issue of underreporting to VAERS has been highlighted for over 30 years and is still an ongoing problem, making reliable statistics regarding vaccine adverse reactions hard to come by. The CDC has now created a new smartphone-based tool used to track adverse events following COVID-19 vaccines called V-safe. At first glance, V-safe may seem like a welcome development: a modern tool that should easily allow vaccine recipients to report, and CDC to track, any adverse events experienced following a vaccination. However, there are serious potential problems created by V-safe.
For all intents and purposes, V-safe intercepts reports that would have otherwise been made by vaccine recipients into VAERS. Only if the CDC deems an adverse event reported to V-safe worthy will it be added to the VAERS database. This leaves a large universe of data regarding adverse events outside of VAERS and outside the public’s view.