EMA head grilled over damning data from EU’s 1st Pfizer/BioNTech vaccine safety report at the European Parliament
On March 27, a 3-hour session held by the ‘Special Committee on COVID-19 pandemic’ took place at the European Parliament.
The last memorable session was when Pfizer’s President of International Developed Markets- “working at the speed of science”-Janine Smalls (who stood in for company CEO Albert Bourla because he failed to show) faced a grilling from certain MEPs. This time it was Emer Cooke’s (former Big Pharma lobbyist, now Executive Director of the European Medicines Agency) turn to be questioned.
Michele Rivasi, MEP and Vice-Chair of the Special Committee on the COVID-19 pandemic: lessons learned and recommendations for the future dropped damning COVID-19 vaccine adverse event data on the floor of the parliament culminating in the fundamental question aimed at Ms Cooke and her agency: how could the EMA conclude a favourable safety profile of the vaccine given the troubling data found in the first-ever EU Pfizer/BioNTech vaccine safety report?
Rivasi’s office informed me that her questions to the EMA head, were drawn from my analysis (first published in Children’s Health Defense Europe) of the bombshell EU report, which contained damning data reported during the first 6 months of 2021.
Below is my overview of the alarming data found in the 286-page report.
Rivasi made a point of highlighting the alarming pregnancy outcome data from the clinical trials, referenced in my analysis. During the 6 month reporting period, 26 pregnancy outcomes from the 149 unique pregnancy cases, were recorded. Of those 26 outcomes, 15 resulted in spontaneous abortion (miscarriage) and 5 of the pregnancy outcomes resulted in live births with congenital anomalies.
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