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Subject European Medicines Agency Data Shows 1,163,356 Adverse Drug Reactions and 30,551 Fatalities by COVID-19 Vaccinations

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[quote:Windir:MV80OTYwMTkyXzExQUMxMDZC]
[b]The official European Union database of suspected drug reaction website is now reporting 30,551 fatalities and 1,163,356 adverse drug reactions from COVID vaccines Pfizer, Moderna, Johnson & Johnson, and AztraZeneca through November 13, 2021 based on the data submitted to its system.[/b]

According to European Medicines Agency, an official website of the European Union, the data of adverse reaction from COVID-19 vaccines were posted in ADRreports.eu portal that “allows users to view the total number of individual suspected side effect reports (also known as Individual Case Safety Reports, or ICSRs).”

All the data shown in the website and individual case report forms were taken from EudraVigilance, “a system designed for collecting reports of suspected side effects, used for evaluating the benefits and risks of medicines during their development and monitoring their safety following their authorization in the European Economic Area (EEA).”

https://www.thegatewaypundit.com/2021/11/european-medicines-agency-data-shows-1163356-adverse-drug-reactions-30551-fatalities-covid-19-vaccinations/
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Original Message The official European Union database of suspected drug reaction website is now reporting 30,551 fatalities and 1,163,356 adverse drug reactions from COVID vaccines Pfizer, Moderna, Johnson & Johnson, and AztraZeneca through November 13, 2021 based on the data submitted to its system.

According to European Medicines Agency, an official website of the European Union, the data of adverse reaction from COVID-19 vaccines were posted in ADRreports.eu portal that “allows users to view the total number of individual suspected side effect reports (also known as Individual Case Safety Reports, or ICSRs).”

All the data shown in the website and individual case report forms were taken from EudraVigilance, “a system designed for collecting reports of suspected side effects, used for evaluating the benefits and risks of medicines during their development and monitoring their safety following their authorization in the European Economic Area (EEA).”

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