NOTE:
The original article at the link below includes gruesome details on vaccine side effects. I have presented a short summary
Ye Editor
Source:
Here is the summary of data through November 13, 2021.
Total reactions for the mRNA vaccine Tozinameran (code BNT162b2, Comirnaty) from BioNTech/ Pfizer:
14,303 fatalities and 562,213 cases of adverse reaction to 11/13/2021 as identified in EudraVigilance:
Total reactions for the mRNA vaccine mRNA-1273(CX-024414) from Moderna:
8,385 fatalities and 155,793 adverse reaction to 11/13/2021:
Total reactions for the COVID-19 vaccine JANSSEN (AD26.COV2.S) from Johnson & Johnson:
1,793 fatalities and 37,038 adverse reaction to 11/13/2021:
Total reactions for the vaccine AZD1222/VAXZEVRIA (CHADOX1 NCOV-19) from Oxford/ AstraZeneca:
6,070 fatalities and 408,312 cases to 11/13/2021:
Summary of cases and fatalities of each vaccine:
As reported from Health Impact News, “the fatalities are grouped by symptoms, and some fatalities may have resulted from multiple symptoms.”
"The official European Union database of suspected drug reaction website is now reporting 30,551 fatalities and 1,163,356 from COVID vaccines Pfizer, Moderna, and 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).
The information were submitted electronically to EudraVigilance by “national medicines regulatory authorities and by pharmaceutical companies that hold marketing authorisations (licences) for the medicines.”
From ADRreports website:
... A side effect is classified as ‘serious’ if it
(i) results in death,
(ii) is life-threatening,
(iii) requires hospitalisation or prolongation of existing hospitalisation,
(iv) results in persistent or significant disability/incapacity (as per reporter’s opinion), (v) is a congenital anomaly/birth defect, or
(vi) results in some other medically important conditions.
A report from Health Impact News mentioned that the database maintained at EudraVigilance is only for countries in Europe who are part of the European Union (EU), which comprises 27 countries.
That means, adverse reaction from the COVID vaccines would be much higher if we include all countries in Europe."
"The official European Union database of suspected drug reaction website is now reporting 30,551 fatalities and 1,163,356 from COVID vaccines Pfizer, Moderna, and 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).
The information were submitted electronically to EudraVigilance by “national medicines regulatory authorities and by pharmaceutical companies that hold marketing authorisations (licences) for the medicines.”
From ADRreports website:
... A side effect is classified as ‘serious’ if it
(i) results in death,
(ii) is life-threatening,
(iii) requires hospitalisation or prolongation of existing hospitalisation,
(iv) results in persistent or significant disability/incapacity (as per reporter’s opinion), (v) is a congenital anomaly/birth defect, or
(vi) results in some other medically important conditions.
A report from Health Impact News mentioned that the database maintained at EudraVigilance is only for countries in Europe who are part of the European Union (EU), which comprises 27 countries.
That means, adverse reaction from the COVID vaccines would be much higher if we include all countries in Europe."
