EU-ADVERSE-REACTIONS-REPORT-COVID-19-mRNA-VACCINATIONS-04-06-2022[92257].pdf

Hendrikus Erik of the House Boomsma 4th. June 2022 – Lelystad, The Netherlands

EU COVID-19 VACCINATION ADVERSE REACTIONS REPORT Source: EudraVigilance – European Medicine Agency (EMA)/ European Union (EU) (DATED 4 JUNE 2022) A. General introduction This report is presenting the details of adverse reactions of the experimental Covid-19 vaccines from AstraZeneca (CHADOX1 NCOV-19), Pfizer (Tozinameran), Moderna (CX-024414) and Janssen (AD26.COV2.S), which have been registered in the adverse reactions reporting/registration system EudraVigilance of the European Medicine Agency (EMA) from the European Union. From March 2021 till March 2022, these reporting/registration details from EudraVigilance have been documented on a weekly basis. And as of April 2022, the information is updated monthly. This report is updated on 4 June 2022. All detailed line listing data have been exported out of the EudraVigilance reporting/registration system and carefully stored in different datafiles worldwide. Details are presented per country, per brand and per main reaction group and per age group. The total number of adverse reactions as well as the total number of individual cases is registered, and that gives an indication of the average adverse reactions per individual case. The overall reported/registered numbers of adverse reactions and deaths is truly shocking, as you will see.

Where during the Swine-Flu pandemic from 2009 “only” 60 deaths were enough to stop the injection campaign with the experimental “Pandemix”-vaccine…, we see now, during the COVID-19 pandemic, no appropriate action is taken to stop the injection campaign with the experimental COVID-19 mRNA vaccines, even when almost 4.5 Million adverse reactions and over 27 Thousand deaths have been reported and registered in EudraVigilance. The justified question therefore remains: “What is going on? And why has no appropriate action been taken?”

B. Underreporting It is a well-known and documented fact that only a small percentage of all adverse reactions of vaccination adverse reactions are in fact reported in reporting/registration systems such as EudraVigilance. In order to estimate the real quantity of adverse reactions, it is therefore important to estimate the percentage of underreporting of EudraVigilance. The estimated underreporting of the EudraVigilance is in this report estimated at 94% and 3 references have been used for determination of this percentage: 1.

Under-reporting of adverse drug reactions : a systematic review (Lorna Hazall; Saad A W Shakir). “In total, 37 studies using a wide variety of surveillance methods were identified from 12 countries. These generated 43 numerical estimates of under-reporting. The median under-reporting rate across the 37 studies was 94%.” Link: (https://pubmed.ncbi.nlm.nih.gov/16689555/)

2.

Electronic Support for Public Health–Vaccine Adverse Event Reporting System (ESP:VAERS) (Harvard Pilgrim Health Care, Inc. / Lazarus, Ross, MBBS, MPH, MMed, GDCompSci, Michael Klompas, MD, MPH; Steve Bernstein). “Fewer than 1% of vaccine adverse events are reported.” Link: (https://digital.ahrq.gov/sites/default/files/docs/publication/r18hs017045-lazarus-final-report-2011.pdf) 3.

Vaccination Numbers vs Individual cases Comparison of total number of fully vaccinated people per EU-country versus the total number of reporting/registration of individual cases of adverse reactions as reported in EudraVigilance. Link: (See section H of this report and https://www.laenderdaten.de/gesundheit/corona-impfungen.aspx) 1

Hendrikus Erik of the House Boomsma 4th. June 2022 – Lelystad, The Netherlands

C. Overall data across 4 vaccines: Overall ABSOLUTE numbers of adverse reactions due to injections with experimental mRNA-vaccines from AstraZeneca (CHADOX1 NCOV-19), Pfizer (Tozinameran), Moderna (CX-024414) and Janssen (AD26.COV2.S) as registered in EudraVigilance from starting injection campaign 2021 till 4 June 2022:

1.

The total number of reported main group adverse reactions The total number of reported individual cases The average number of main group adverse reaction per individual case

: : :

4.414.030 1.826.581 2,4

2.

The total number of reported main group adverse reactions leading to death The total number of reported deaths The average number of main group adverse reactions leading to death

: : :

45.316 27.079 1,7

Overall ESTIMATED REAL numbers of adverse reactions due to injections with experimental mRNA-vaccines from AstraZeneca (CHADOX1 NCOV-19), Pfizer (Tozinameran), Moderna (CX-024414) and Janssen (AD26.COV2.S) BASED ON UNDERREPORTING OF 94 % from starting injection campaign 2021 till 4 June 2022:

1.

The total number of reported main group adverse reactions The total number of reported individual cases The average number of main group adverse reaction per individual case

: : :

73.567.167 30.443.017 2,4

2.

The total number of reported main group adverse reactions leading to death The total number of reported deaths The average number of main group adverse reactions leading to death

: : :

755.267 451.317 1,7

2

Hendrikus Erik of the House Boomsma 4th. June 2022 – Lelystad, The Netherlands

Fig. 1

Fig. 2

3

Hendrikus Erik of the House Boomsma 4th. June 2022 – Lelystad, The Netherlands

D. Details regarding AstraZeneca (CHADOX1 NCOV-19) Overall ABSOLUTE numbers of adverse reactions due to injections with experimental mRNA-vaccines from AstraZeneca (CHADOX1 NCOV-19), as registered in EudraVigilance from starting injection campaign 2021 till 4 June 2022: 1.

The total number of reported main group adverse reactions The total number of reported individual cases (Fig. 1) The average number of main group adverse reaction per individual case

: : :

1.280.160 493.367 2,6

2.

The total number of reported main group adverse reactions leading to death The total number of reported deaths The average number of main group adverse reactions leading to death

: : :

9.033 5.846 1,6

Overall ESTIMATED REAL numbers of adverse reactions due to injections with experimental mRNA-vaccines from AstraZeneca (CHADOX1 NCOV-19) BASED ON UNDERREPORTING OF 94 % from starting injection campaign 2021 till 4 June 2022: 1.

The total number of estimated real main group adverse reactions The total number of estimated real individual cases The average number of main group adverse reaction per individual case

: : :

21.336.000 8.222.783 2,6

2.

The total number of estimated real main group adverse reactions leading to death The total number of estimated real deaths The average number of main group adverse reactions leading to death

: : :

150.550 97.433 1,6

Fig. 3

4

Hendrikus Erik of the House Boomsma 4th. June 2022 – Lelystad, The Netherlands

E. Details regarding Pfizer (Tozinameran) Overall ABSOLUTE numbers of adverse reactions due to injections with experimental mRNA-vaccines from Pfizer (Tozinameran), as registered in EudraVigilance from starting injection campaign 2021 till 4 June 2022: 1.

The total number of reported main group adverse reactions The total number of reported individual cases (Fig. 1) The average number of main group adverse reaction per individual case

: : :

2.244.030 971.864 2,3

2.

The total number of reported main group adverse reactions leading to death The total number of reported deaths The average number of main group adverse reactions leading to death

: : :

21.333 13.502 1,6

Overall ESTIMATED REAL numbers of adverse reactions due to injections with experimental mRNA-vaccines from Pfizer (Tozinameran), BASED ON UNDERREPORTING OF 94 % from starting injection campaign 2021 till 4 June 2022: 1.

The total number of estimated real main group adverse reactions The total number of estimated real individual cases The average number of main group adverse reaction per individual case

: : :

37.400.500 16.197.733 2,3

2.

The total number of estimated real main group adverse reactions leading to death The total number of estimated real deaths The average number of main group adverse reactions leading to death

: : :

355.550 225.033 1,6

Fig. 4

5

Hendrikus Erik of the House Boomsma 4th. June 2022 – Lelystad, The Netherlands

F. Details regarding Moderna (CX-024414) Overall ABSOLUTE numbers of adverse reactions due to injections with experimental mRNA-vaccines from Moderna (CX-024414), as registered in EudraVigilance from starting injection campaign 2021 till 4 June 2022: 1.

The total number of reported main group adverse reactions The total number of reported individual cases (Fig. 1) The average number of main group adverse reaction per individual case

: : :

732.849 300.012 2,4

2.

The total number of reported main group adverse reactions leading to death The total number of reported deaths The average number of main group adverse reactions leading to death

: : :

12.010 6.265 1,9

Overall ESTIMATED REAL numbers of adverse reactions due to injections with experimental mRNA-vaccines from Moderna (CX-024414), BASED ON UNDERREPORTING OF 94 % from starting injection campaign 2021 till 4 June 2022: 1.

The total number of estimated real main group adverse reactions The total number of estimated real individual cases The average number of main group adverse reaction per individual case

: : :

12.214.150 5.000.200 2,4

2.

The total number of estimated real main group adverse reactions leading to death The total number of estimated real deaths The average number of main group adverse reactions leading to death

: : :

200.167 104.417 1,9

Fig. 5

6

Hendrikus Erik of the House Boomsma 4th. June 2022 – Lelystad, The Netherlands

G. Details regarding Janssen (AD26.COV2.S) First, an important note has to be made regarding the registration details of adverse reactions due to the injections with the Janssen vaccines. Since 16th. May 2022, there have been 630 previous registered deaths removed from the EudraVigilance system. No clarification or reason for this has been published by the EMA.

Overall ABSOLUTE numbers of adverse reactions due to injections with experimental mRNA-vaccines from Janssen (AD26.COV2.S), as registered in EudraVigilance from starting injection campaign 2021 till 4 June 2022: 1.

The total number of reported main group adverse reactions The total number of reported individual cases (Fig. 1) The average number of main group adverse reaction per individual case

: : :

156.991 61.338 2,6

2.

The total number of reported main group adverse reactions leading to death The total number of reported deaths The average number of main group adverse reactions leading to death

: : :

2.940 1.466 1,9

Overall ESTIMATED REAL numbers of adverse reactions due to injections with experimental mRNA-vaccines from Janssen (AD26.COV2.S), BASED ON UNDERREPORTING OF 94 % from starting injection campaign 2021 till 4 June 2022: 1.

The total number of estimated real main group adverse reactions The total number of estimated real individual cases The average number of main group adverse reaction per individual case

: : :

2.616.517 1.022.300 2,6

2.

The total number of estimated real main group adverse reactions leading to death The total number of estimated real deaths The average number of main group adverse reactions leading to death

: : :

49.000 24.433 1,9

Fig. 6 7

Hendrikus Erik of the House Boomsma 4th. June 2022 – Lelystad, The Netherlands

H. Vaccination Numbers vs Reported individual cases of adverse reactions per EU-Country Figure 7. shows an overview on the absolute number of vaccinated people per EU-country as reported by the German Ministery of Health (Bundesministerium für Gesundheid) and Zeitverlag Gerd Bucerius GmbH & Co. KG and shown on the websites: Link: https://impfdashboard.de/ Link: https://www.zeit.de/wissen/gesundheit/corona-impfungen-aktuelle-zahlen-deutschland-karte Link: https://www.laenderdaten.de/gesundheit/corona-impfungen.aspx The comparison of the total number of fully vaccinated people versus the total number of individual cases of adverse reactions per EU country confirms clearly a grave underreporting. Moreover – based on an average underreporting of 94 % - the overview shows that…: 1 : 11 vaccinated individuals suffered one or more adverse reactions. 1 : 728 vaccinated individuals have died from one or more adverse reactions Based on these estimations, it is estimated that on a global scale, approximately 6.553.955 individuals died to date, from the adverse reactions from the injections with COVID-19 mRNA vaccines from AstraZeneca (CHADOX1 NCOV-19), Pfizer (Tozinameran), Moderna (CX-024414) and Janssen (AD26.COV2.S). And these numbers are still rising!!

Fig. 7

8

Hendrikus Erik of the House Boomsma 4th. June 2022 – Lelystad, The Netherlands

I. Recommendations to Policy Makers, Health Officials and the General Public 1. The reported and registered ABSOLUTE numbers of adverse reactions caused by the injections with the experimental COVID-19 mRNA substances from AstraZeneca (CHADOX1 NCOV-19), Pfizer (Tozinameran), Moderna (CX-024414) and Janssen (AD26.COV2.S), the number of individual cases of people suffering from these adverse reactions and even death, are disastrous and beyond imagination. They must lead to an immediate total and worldwide ban of further injecting people with these dangerous substances. 2. Estimated REAL numbers of the adverse reactions from these injections (due to severe underreporting), indicate that the reality of the damage caused by these injections is monstrous and even up to a scale of WORLDWIDE GENOCIDAL PROPORTIONS. Therefore, a full investigation of the disastrous consequences of the worldwide vaccination injection-campaign, by an International Investigation Committee of totally independent investigators, detectives, scientists, legists, jurors and representatives of both victims, non-vaccinated people and the general public has to be conducted.

Since it is obvious that many policy makers, health care officials, officials from authorisation institutes, major shareholders of Media-, Big Tech-, and Pharmaceutical companies, et cetera, are directly or sideways involved in the matter of this injection-campaign, they should all be excluded from membership of this International Investigation Committee. 3. Based on the outcome and conclusions of the International Investigation Committee as above mentioned, all individuals who have participated directly or indirectly to the injection-campaign and carry responsibility for the disastrous health consequences and damage to individuals, must be brought to justice in an International Court of Justice or Special Dedicated Tribunal.

9