VAERS: Two-Year-Old Dies After Receiving COVID-19 & Flu Shots

A two-year-old child passed away after receiving BOTH the COVID-19 shot and annual influenza shot, according to VAERS.

The female toddler from New Hampshire reportedly took the experimental Moderna COVID-19 mRNA gene therapy and GlaxoSmithKline seasonal FluLaval Quadrivalent influenza vaccine.

When is this going to stop? #ProsecuteFauci https://t.co/1oifbnjSWp pic.twitter.com/xOWNaVL1L9

— Chief Nerd (@TheChiefNerd) January 7, 2023

VAERS ID: 2536846 stated:

Death after receiving both COVID and annual Influenza vaccines

The experimental COVID-19 shots have created a “humanitarian catastrophe,” said Dr. Pierre Kory.

“CDC Releases Its VAERS Safety Analyses for COVID Vaccines via FOIA,” he added.

The scope and scale of the humanitarian catastrophe caused by the global Covid vaccine campaign is in even plainer sight now. But are the ears and eyes of U.S citizens fully open yet?

CDC Releases Its VAERS Safety Analyses for COVID Vaccines via FOIA https://t.co/ZBpakBafOk

— Pierre Kory, MD MPA (@PierreKory) January 4, 2023

Josh Guetzkow summarized the CDC’s VAERS safety signal analysis on Jackanapes Junction:

• CDC’s VAERS safety signal analysis based on reports from Dec. 14, 2020 – July 29, 2022 for mRNA COVID-19 vaccines shows clear safety signals for death and a range of highly concerning thrombo-embolic, cardiac, neurological, hemorrhagic, hematological, immune-system and menstrual adverse events (AEs) among U.S. adults.
• There were 770 different types of adverse events that showed safety signals in ages 18+, of which over 500 (or 2/3) had a larger safety signal than myocarditis/pericarditis.
• The CDC analysis shows that the number of serious adverse events reported in less than two years for mRNA COVID-19 vaccines is 5.5 times larger than all serious reports for vaccines given to adults in the US since 2009 (~73,000 vs. ~13,000).
• Twice as many mRNA COVID-19 vaccine reports were classified as serious compared to all other vaccines given to adults (11% vs. 5.5%). This meets the CDC definition of a safety signal.
• There are 96 safety signals for 12-17 year-olds, which include: myocarditis, pericarditis, Bell’s Palsy, genital ulcerations, high blood pressure and heartrate, menstrual irregularities, cardiac valve incompetencies, pulmonary embolism, cardiac arrhythmias, thromboses, pericardial and pleural effusion, appendicitis and perforated appendix, immune thrombocytopenia, chest pain, increased troponin levels, being in intensive care, and having anticoagulant therapy.
• There are 66 safety signals for 5-11 year-olds, which include: myocarditis, pericarditis, ventricular dysfunction and cardiac valve incompetencies, pericardial and pleural effusion, chest pain, appendicitis & appendectomies, Kawasaki’s disease, menstrual irregularities, vitiligo, and vaccine breakthrough infection.
• The safety signals cannot be dismissed as due to “stimulated,” exaggerated, fraudulent or otherwise artificially inflated reporting, nor can they be dismissed due to the huge number of COVID vaccines administered. There are several reasons why, but the simplest one is this: the safety signal analysis does not depend on the number of reports, but whether or not some AEs are reported at a higher rate for these vaccines than for other non-COVID vaccines. Other reasons are discussed in the full post below.
• In August, 2022, the CDC told the Epoch Times that the results of their safety signal analysis “were generally consistent with EB [Empirical Bayesian] data mining [conducted by the FDA], revealing no additional unexpected safety signals.” So either the FDA’s data mining was consistent with the CDC’s method—meaning they “generally” found the same large number of highly alarming safety signals—or the signals they did find were expected. Or they were lying. We may never know because the FDA has refused to release their data mining results.

“CDC identified hundreds of safety signals for Pfizer and Moderna COVID vaccines. Bell’s palsy, blood clotting and death were among the signals flagged through analysis of adverse event reports submitted to VAERS,” Robert F. Kennedy Jr. tweeted.

Yep! CDC identified hundreds of safety signals for Pfizer and Moderna COVID vaccines. Bell’s palsy, blood clotting and death were among the signals flagged through analysis of adverse event reports submitted to VAERS.https://t.co/VqDD8746DL

— Robert F. Kennedy Jr (@RobertKennedyJr) January 3, 2023

The Epoch Times noted, via The Defender:

U.S. health officials have been cautious in tying adverse events, or side effects, to the COVID-19 vaccines.

But they have acknowledged that some side effects are caused by the Moderna and Pfizer vaccines — both of which utilize messenger RNA (mRNA) technology — including myocarditis and a related condition called pericarditis.

Some age groups are actually at higher risk of myocarditis and pericarditis after vaccination than after COVID-19 infection, leading a growing number of experts to warn against vaccinating certain people.

The newly obtained PRR results returned more than 500 adverse events larger than myocarditis and pericarditis.

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“We know that the signal for myocarditis is associated with something that is caused by the mRNA vaccines, so it’s more than reasonable to say that anything with a signal larger than myocarditis/pericarditis should be taken seriously and investigated,” Josh Guetzkow, an Israeli professor who trained in statistics at Princeton University and has been studying VAERS data during the pandemic, told The Epoch Times via email.

The CDC and FDA said in their operating procedures that safety signals would be “reviewed as appropriate.”

“The pattern or trend of PRR and data mining results over a period of time (e.g., several weeks) will be monitored before initiating a clinical review. Other factors, such as clinical importance, whether AEs are unexpected, seriousness, and whether a specific syndrome or diagnosis is identified rather than non-specific symptoms will be considered in determining if clinical review will be performed,” the documents stated.

If a clinical review was triggered, that would include reviewing reports and associated medical records regarding the adverse event, confirming time from vaccination to symptoms onset and other work.

Despite mountains of evidence that the COVID-19 jab rollout created an unprecedented health disaster, the shots remain available.

And horrific tragedies, such as the two-year-old girl from New Hampshire, continue showing up in the VAERS reports.