EXCLUSIVE – 100% of Covid-19 Vaccine Deaths were caused by just 5% of the batches produced according to official Government data
(The Expose UK, Oct 31, 2021)
An investigation of data found in the USA’s Vaccine Adverse Event Reporting System (VAERS) has revealed that extremely high numbers of adverse reactions and deaths have been reported against specific lot numbers of the Covid-19 vaccines several times, meaning deadly batches of the experimental injections have now been identified.
But what’s perhaps more concerning is that the “deadly” lots were distributed widely across the United States whilst other “benign” lots were sent to just a few locations.
The data used in the investigation was pulled from the publicly accessible VAERS database which can be viewed here. The Vaccine Adverse Event Reporting System (VAERS) is a United States programme for vaccine safety, co-managed by the U.S. Centers for Disease Control and Prevention (CDC) and the Food and Drug Administration (FDA).
The programme collects information via reports made by doctors, nurses, and patients about adverse events (possible harmful side effects) that occur after administration of vaccines to ascertain whether the risk–benefit ratio is high enough to justify continued use of any particular vaccine.
The reports pulled from the database were ones that had been submitted up to October 15th 2021 and they included all adverse reactions reported against the Pfizer and Moderna mRNA Covid-19 injections, as well as all adverse reactions reported against the influenza vaccines; which were used to generate a control dataset .
The VAERS database showed a total of 1,608 adverse event reports against the flu vaccines alongside 15 deaths and 73 hospitalisations. The total count of lot numbers returned was 494.
The ‘lot number’ is a specific string of numbers and letters that tracks a specific batch of vaccine from production and into a persons arm and it is usually found on a vaccine label or accompanying packaging.
The above chart shows the number of adverse event report made to VAERS against the influenza vaccines sorted by the lot number of vaccine that was administered prior to the adverse event.
Except for a few spikes the number of adverse events per lot number was generally the same, with no more than 26 reports being made against a single lot number of influenza vaccine.