Europe – AdverseEffects

In the USA there is the official Vaccine Adverse Event Reporting System / VAERS a data base for the vaccine adverse event reports in the USA. Unfortunately it is not very well known, even doctors often do not know about its existence and it is not used very often. A research study by Harvard University concluded years ago that fewer than 1% of all cases are reported in the VAERS system.
The Vaccine Adverse Events Reporting System in the EU is called EudraVigilance and is provided by the European Medicines Agency / EMA. The reporting system of the EU is equally underused and not well known. It is estimated that only about 5% to 10% of the cases are registered in the EU database.
Pharmaceutical companies are required to use the databases for adverse event reports, but they also provide and recommend the V-Save App to the vaccinated. It is not clear how and where these reports are collected and whether they end up in VAERS and EudraVigilance.
It is possible to retrieve a wide variety of information from both databases, but it is relatively cumbersome in both systems. In the EU system, you even have to add up the individual reactions of the individual vaccinations.
In intervals of about four weeks we check the databases, collect, and calculate the umbers and provide the latest figures on our website. So please check back often!
Considering the fact, that only a fraction of the actual adverse events are being reported, we have to assume that all the numbers we are collecting are always too low. In our graph with the combined numbers from Europa and USA you also will find a projection in the event that the reports actually account only for 1% or 10% of the cases.