391,000 severe vaxx adverse events in Europe during first 6 months of roll-out

APRIL 15, 2023, The Spotlight Conference, Stavanger Norway. Investigative journalist Sonia Elijah shows results from the first-ever periodic safety report of the European Union (EU) on the COVID 'vaccines'. These documents only became available to the public recently thanks to a freedom of information request.

Summary of the results:

- 327,827 case reports (individuals) containing a whopping 1,172,887 adverse events
- Strong disparity between men and women: Three times more cases reported for women than for men
- Highest number of reported cases in the 31-50 age group. This age group has a very low risk of a severe outcome of COVID, so very little to benefit (but unlimited risk) from vaccination.
- A third of all case reports were classified as serious, so that's almost 400,000 severe adverse events. Note that probably at most 10% of severe adverse events are reported, so the real number of adverse events among European citizens is probably more than 4 MILLION.
- 44% of case reports were classified as serious
- 84% of case reports had no history of comorbidities. This group has a very low risk of a severe outcome of COVID, so very little to benefit (but unlimited risk) from vaccination.
- 5115 deaths occurred after 'vaccine' was administered
- 46% of fatal outcomes occurred in those without any comorbidities

In spite of all these horrible results, the EMA still conclude "...the benefit-risk profile of BNT162b2 [Pfizer-BioNTech 'vaccine'] remains favourable". They must be talking about the benefit-risk profile of the manufacturer, not of the injected.

The report is also guilty of gaslighting. It acknowledges many reports of menstrual disorders, abnormal bleeding for women. Instead of relating it to the injection, they blame "stress during the pandemic".

There is also a strong lot variability. One lot had over 16,000 adverse events, but still the report concluded, "There is no related quality issue identified during investigation".

The report is correct. After all, that lot was just a financially profitable to the manufacturer, so there is no problem. Sure, it destroyed health, but judging from their behavior, neither the manufacturer nor the regulator care about these things. In fact, destroyed health is a feature, not a bug, because sick people buy highly profitable medicines.

REFERENCES

EMA’s failure to pull COVID 19 jabs even though risk-benefit balance nullified
https://childrenshealthdefense.eu/eu-issues/emas-failure-to-pull-covid-19-jabs-even-though-risk-benefit-balance-nullified/

The many untruths told by EMA Head, Emer Cooke
https://soniaelijah.substack.com/p/the-many-untruths-told-by-ema-head

SOURCE: https://rumble.com/v2m06ay