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Many thanks to Hellequin GB for translating this German-language article from Report24:
Particularly deadly vaccine batches were injected less often — who knew?
A study from Denmark shows: Individual batches of Pfizer’s so-called “Covid-19 vaccine” Comirnaty (BNT162b2) have a particularly problematic safety profile. This is due to the accumulation of severe side effects. The differences with less problematic batches are statistically extremely significant. Under normal circumstances, the mere fact that these variations exist would be a warning sign and reason for a recall of the product. But worse: there seem to be accomplices.
The study, which has criminality potential, can be found under the name “Batch-dependent safety of the BNT162b2 mRNA COVID-19 vaccine”. The scientists involved are the Danes Max Schmeling, Vibeke Manniche and Peter Riis Hansen.
First of all, it should be noted that in Europe alone, as of November 11, 2022, there have been 971,021 reports of serious adverse events. The approach of the investigation briefly explained:
Not least with regard to the emergency market approval and the rapid implementation of large-scale vaccination programs, however, the possibility of a batch-dependent variation seems worthy of investigation.
Study “Batch-dependent Safety of BNT162b2 mRNA COVID-19 Vaccine”
The investigation deals with the side effect reports in Denmark from December 27, 2020 to January 11, 2022. These are recorded in the state safety database DKMA and classified according to severity. The batch number is also saved there with the suspicious activity reports. Classifications include: Non-serious, severe (involving hospitalization, life-threatening illness, permanent disability, or congenital malformation), and death.
A total of 7,835,280 doses were administered to 3,748,215 subjects using 52 different BNT162b2 vaccine batches (2,340-814,320 doses per batch) and 43,496 serious adverse reactions were recorded in 13,635 subjects.
A total of 66,587 side effects were spread across 52 batches, meaning that when multiple doses were administered, individuals suffered and severe side effects were recorded each time.
The evaluation of this data made it possible, after excluding all reports without batch numbers, to assign 61,847 reported serious side effects to the respective batches. Of the serious side effects, 14,509 (23.5%) were classified as serious and 579 (0.9%) as fatal.
Result indicates complicity
The scientists would have expected that the vaccine “quality” would be largely identical in all batches and that the occurrence of side effects would therefore be equally distributed. This would also be expected from a properly approved and tested active substance. The result was all the more surprising.
However, the number of serious side effects reported varied significantly between batches of the vaccine, ranging from 0.09 to 3.59 per 1,000 doses administered. This difference is dramatic and can only be explained by extremely different vaccine quality.