Just 6% of the batches of Covid-19 Vaccine produced have caused every single Adverse Reaction suffered by Children resulting in Permanent Disability or Death
An investigation of data found in the USA’s Vaccine Adverse Event Reporting System (VAERS) suggests foul play by the vaccine manufactuers and that they are conducting a real-world experiment on children to determine what dosage is required to cause injury or death.
This is because extremely high numbers of adverse reactions, hospitalisations, life threatening events, permanent disabilities, and deaths among children have been reported against specific lot numbers of the Covid-19 vaccines many times. and the data reveals that every single reported adverse reaction resulting in permanent disability or death has been caused by just 6% of the specific batches of Covid-19 vaccine produced and administered to children.
This means the most dangerous and deadliest batches of the experimental injections being administered to children have now been identified.
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 November 5th 2021 and they included all adverse reactions reported against the Pfizer Covid-19 injections among children aged 6 to 17.
But first a control dataset was created using all adverse reactions reported against all influenza vaccines administered to all children aged 6 to 17 during 2019 and 2020, a period of two years.
We can be confident that many more influenza injections were administered to children during this time frame, than Covid-19 injections have been administered to children during 2021, due to confirmation in official data published by the Centers for Disease Contol (CDC).
The publication released by the CDC (see here) in October 2020 confirms that in the 19/20 flu season, 63.8% of children aged 6 months – 17 years, received a dose of the flu jab. The data we’ve extracted also include figures from the 18/19 flu season of which 62.6% of children aged 6 months – 17 years received a flu jab, and the 20/21 flu season of which the number of children to receive a flu jab is unknown.
The VAERS database showed a total of 2,082 adverse event reports against the flu vaccines among children alongside 278 emergency room visits, 45 hospitalisations, 11 life threatening events, 17 permanent disabilities, and 2 deaths. The total count of lot numbers returned was 802.
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 reports made to VAERS against the influenza vaccines among children, sorted by the lot number of vaccine that was administered prior to the adverse event.
The lot numbers are sorted alphabetically and except for a few spikes the number of adverse events per lot number were evenly distributed and generally the same, with no more than 17 reports being made against a single lot number of influenza vaccine.
The above chart shows the number of hospitalisations reported as adverse reactions to the Pfizer vaccine by lot number sent across the USA. This chart has identified the actual lot numbers of influenza vaccine that caused children to be hospitalised.
As you can see, just a single lot number ‘3GG33’ had more than 1 hospitalisation report against it but this only amounted to 2 hospitalisations. Whilst a further 33 lot numbers caused a single hospitalisation.
All of the above data on adverse reactions to the influenza vaccine among children over a period of two years was used as a control dataset to compare against VAERS data for the Pfizer Covid-19 vaccine.
The VAERS database showed a total of 16,880 adverse event reports against the Pfizer Covid-19 vaccine among children aged 6-17. These included 5,161 emergency room visits, 1,365 hospitalisations, 264 life threatening events, 120 permanent disabilities, and 29 deaths. The total count of lot numbers returned was 748.
The Food and Drug Administration (FDA) granted emergency use authorisation for the Pfizer Covid-19 injection to be administered to children over the age of 12 on the 10th may 2021.
This means that in a period of 6 months there have been –
8 times as many adverse reactions,
18 times as many emergency room visits,
30 times as many hospitalisations,
24 times as many life threatening events,
7 times as many permanent disabilities, and
15 times as many deaths due to the Pfizer jab than what has been recorded among children against the influenza vaccines over a period of two years.
The above chart shows the number of adverse event reports made to VAERS against the Pfizer Covid-19 vaccine among children, sorted by the lot number of vaccine that was administered prior to the adverse event.
The highest number of adverse event reports made to VAERS against a single lot number of the influenza vaccine was 17. Which makes it all the more shocking to discover that the highest number of adverse event reports made to VAERS against a single lot number of the Pfizer Covid-19 vaccine up to November 5th 2021 was 428, and this isn’t an anomaly.
Hundreds of adverse event reports have been made against a single lot number of the Pfizer Covid-19 vaccine numerous times.
The above chart shows the count of lots against the range of adverse events reported per lot of Pfizer Covid-19 vaccine. The data reveals that 511 lots (68%) had just a single adverse event report made against them, whilst 2 specific lots had over 401 adverse event reports made against them.
Shockingly we can also see from the data that 30 lots of Pfizer vaccine had between 12 separate lots (1.6%) had between 151 – 250 adverse event reports per lot, another 11 lots (1.5%) had between 251 – 350 adverse event reports per lot, and another 7 lots (0.9%) had between 350 – 400 adverse event reports per lot.
This suggests that there were a small quantity of dangerous batches of the Pfizer Covid-19 vaccine and a large quantity of seemingly harmless (at least in the short term) batches of the Pfizer Covid-19 vaccine administered to children.
We can see the same pattern occurring among more serious adverse reactions as well, with only a few separate lot numbers of the Pfizer vaccine being associated with very high numbers of emergency room visits, hospitalisations, life threatening events, permanent disabilities, and deaths.
Emergency Room Visits
356 lots (48%) caused zero emergency room visits among children, and 311 lots (42%) causes between 1 and 4 emergency room visits among children. But 7 lots (0.9) caused over 100 emergency room visits among children per lot.
In all, 52% of the lots of Pfizer vaccine administered to children were responsible for an adverse reaction resulting in an emergency room visit.
585 lots (78%) of the Pfizer jab caused zero hospitalisations among children, and 87 lots (12%) caused just 1 hospitalisation among children. But 5 lots of the Pfizer jab (0.7%) caused over 30 hospitalisations among children per lot.
In all, 22% of the lots of Pfizer vaccine administered to children were responsible for an adverse reaction resulting in hospitalisation.
Life Threatening Events
670 lots (90%) were associated with zero life threatening events among children, and 40 lots (5%) were associated with 1 life threatening event among children. But just 8 lots (1%) were associated with between 5 and 8 life threatening events per lot among children.
In all, 10% of the lots of Pfizer vaccine administered to children were responsible for a life threatening event.
700 lots (94%) caused zero permanent disabilities among children, whilst 29 lots ( 4%) caused a single permanent disability among children. But 4 lots (0.5) caused 4 permanent disabilities per lot, equating to 33% (16/48) of all permanent disabilties reported as adverse reactions to the Pfizer jab among children.
In all, just 6% of the lots of Pfizer vaccine administered to children were responsible for an adverse reaction resulting in the child being left permanently disabled.