CONCLUSION:
"This investigation of VAERS data ... leads to questions of why authorities within the USA which are supposed to monitor the safety of the Covid-19 vaccines have not discovered this themselves.
The data clearly shows that the Covid-19 vaccination campaign has been significantly more harmful and deadly to children than the influenza vaccination campaign.
This fact alone begs the question as to how the FDA advisory committee could possibly vote Seventeen to Zero in favour of approving the Pfizer vaccine for use in children aged 5 to 11.
One voting member of the Food and Drug Administration (FDA) advisory committee, Dr Eric Rubin, of Harvard University said
– “We’re never going to learn how safe the vaccine is unless we start giving it, and that’s just the way it goes”.
But the investigation of VAERS data has also identified the specific batches of Pfizer vaccine that have caused the most harm to children across the USA, which leads to other extremely serious questions requiring urgent answers.
Why is it that certain batches of the vaccine have proven to be more harmful and deadly than others?
Why do the 20 most harmful batches of Pfizer vaccine from the 748 known batches administered to children all have lot numbers that closely correspond?
Ranging from EW0162 to EW0217.
Could this just be a quality control issue?
A Pfizer whistleblower from a Kansas manufacturing facility did after all reveal that “People are being made to sign off on things that normally they wouldn’t, and then they wonder why their own employees won’t take it”.
DETAILS:
NOTE:
Original much longer (too long) article included 26 charts -- only the most important two are shown below:
(1) Influenza shot hospitalizations of children sorted by vaccine lot (very few hospitalizations) and
(2) Prizer Covid vaccine emergency room visits for children sorted by lot (30x higher than Influenza vaccines)
Ye Editor
"An investigation of data found in the USA’s Vaccine Adverse Event Reporting System (VAERS) suggests foul play by the vaccine manufacturers 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.
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 in October 2020 confirms that in the 2019 / 2020 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 2018 / 2019 flu season of which 62.6% of children aged 6 months – 17 years received a flu jab, and the 2020 / 2021 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 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.
... 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 highest number of adverse event reports made to VAERS against a single lot number of the influenza vaccine was 17.
... 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
Hundreds of adverse event reports have been made against a single lot number of the Pfizer Covid-19 vaccine numerous times.
... 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.
... 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.
... 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.
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.
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.
733 lots were associated with zero deaths among children,
but 15 lots were associated with a single death among children.
There were also a further 14 deaths reported of which the lot number was unknown.
This means the minimum number of lots responsible for a death equates to 15 and the maximum possible number is 29.
In all, between 2% (15 lots) and 4% (29 lots) of the lots of Pfizer vaccine administered to children were responsible for an adverse reaction resulting in death.
... the most dangerous batches of Covid-19 vaccine all have lot numbers that closely correspond to each other.
... suggests the most dangerous, and deadlisest batches of the Pfizer vaccine that have been administered to children, and are still being administered to children, were all manufactured in close proximity of each other,
rather than a dangerous batch being manufactured on day 1 and the next dangerous batch being manufactured on day 86.
... The most harmful of which is lot number ‘EW0187’; causing 428 adverse events reports to be made.
.. 19 out of the top 20 lots are all ‘EW’ lot numbers ranging from EW0167 to EW0217.
The one exception is lot number FA6780 which had 344 adverse event reports made against it.
... EW0185 lot caused 137 emergency room visits among children.
...17 out of the 20 lots are all ‘EW’ lot numbers ranging from EW0168 to EW0217.
The three exceptions are lot numbers FA6780, FA7485, and ER8735 which had 92, 83, and 80 emergency room visit reports made against them."
