How Many Babies Survived Pfizer's COVID-19 mRNA Trial?

Source: Karen Kingston

Date: January 13, 2025

January 13, 2025:  Last week I shared the CDC’s disclaimer that “Some Babies Will Experience Death Shortly After Vaccination by Coincidence,” and received numerous inquiries into clinical data that showed infant death post vaccination.

The below 2023 Kingston Report summarizes the horrifying findings of Pfizer’s Phase-3 data in babies as young as 6-months old.

June 18, 2023: In July of 2022 I began reporting on my analysis of Pfizer’s Phase-3 trial data of babies and toddlers from the ages of 6 months to 4 years old. If you have ever seen me report on this data, I typically get teared-up and sometimes need to stop recording. I don’t understand how a human being with a soul could have carried out these criminal experiments on babies and toddlers.

There Was NO Placebo.

All of the babies and toddlers were injected with mRNA nanoparticles BNT162b2 (aka Pfizer’s COVID-19 ‘vaccine’) unless the parents of the babies in the ‘placebo group’ figured out that the trial was essentially infanticide and withdrew their baby or toddler before they were injected with mRNA nanoparticles BNT162b2.

Pfizer and the FDA had Data Showing COVID-19 mRNA Injections Caused Severe Side Effects, Including Death in Babies Before the Babies’ Study Started

Per page 11 of their FDA submission, Pfizer states, “As of May 19, 2022, VAERS received…245 US report in children 6 months through 4 years of age (after vaccination)…

Persons 6 months through 4 years of age; product administered to patient of inappropriate age, exposure via breastmilk, pyrexia (dangerously high fevers), SARS-CoV-2 test, body temperature, off-label use, headache, rash, diarrhea.”

5-Month Old Baby Dies From Vaccinated Mother’s Breast Milk

The FDA and Pfizer reported a VAERS report of ‘exposure via breastmilk’ in an 5-month old baby boy. Per VAERS Case ID #1166062, the day after a mother received her second Pfizer injection, her baby boy developed a rash and became inconsolable after breastfeeding from her. The baby was rushed to the emergency room and bloodwork showed elevated enzymes (potential heart attack?) He died from Thrombosis Thrombocytopenia a painful condition where the 5-month old experienced low red blood cell counts and blood clotting simultaneously.

Pfizer Knew the COVID-19 mRNA Injections Were More Harmful than the Disease Per Early Clinical Trial Data Children

Pfizer stated on November 20, 2020, that according to their clinical trial data in children aged 12-15 years of age, the risk-benefit ratio of mRNA vaccines was not favorable (aka harmful) for children

Despite this damning information, not only did the Pfizer and the FDA move forward with clinical trials and emergency use authorization in pediatric populations, placing children and infants at unnecessary risk for disease, disabilities and death, the FDA also fraudulently granted full FDA approval for Pfizer’s COVID-19 shots for children aged 12-15.

Pfizer Knowingly Placed Children at Unnecessary Risk for Disease and Death

There’s NO Vaccine More Effective Than a Child’s Immune System

On June 10, 2021, the FDA stated that it would be infeasible (impossible) to conduct a clinical trial that would could clinically and statistically prove a vaccine could safely prevent SARS-CoV-2 infection or COVID-19 disease in children (specifically younger pediatric patients, such as infants and toddlers) because pediatric populations rarely became infected with SARS-CoV-2 or presented with COVID-19 symptoms.

70% of Babies and Toddlers Never Made it to the End of Pfizer's Trials

Per Pfizer’s June 15, 2022 data submission to the FDA, Pfizer enlisted 4,526 babies and toddlers to conduct criminal human experimentation on. Completion of the clinical trial was defined as a 2-month follow-up visit post the 3rd dose of BNT162b2.

Of the originally enlisted 4,526 babies and toddlers enlisted, only 1,424 (31%) made it to their 2-month post mRNA dose-3 doctor’s visit.

Throughout the body of this Pfizer document, there are horrifyingly detailed descriptions of the disabling and painful harms done to the babies and toddlers after receiving the mRNA nanoparticle injections, including; anaphylaxis, appendicitis, fevers of greater than 104 degrees Fahrenheit, seizures (with eye rolling), convulsions, and status epilepticus (seizures lasting more than 5 minutes and multiple seizures a day -sometimes a dozen or more- that can lead to permanent brain damage).

Pfizer also documented epilepsy, exanthema subitum (herpes induced fever and seizures), permanent brain damage confirmed by an EEG, hypotonia (limp ‘lifeless-like’ baby), and lissencephaly (genetic-induced brain malformation characterized by the absence of convolutions/folds) in babies and toddlers injected with mRNA nanoparticles.

Why were mRNA Nanoparticle Injections for Babies and Toddlers Authorized in the United States?

Pfizer and the FDA simply ‘agreed’ that these permanently disabling and potentially deadly systemic and neurological outcomes occurring in formerly healthy babies and toddlers within hours, days, or weeks after receiving Pfizer’s mNA nanoparticle injections were not from Pfizer’s mRNA nanoparticle injections.

What Happed to 370 Toddlers Who Were 2 to 4 Years Old?

In an unblinded placebo subgroup of 370 toddlers 2 to 4 years old, 370 toddlers were injected with the 1st dose of 3μg of mRNA nanoparticles, 350 toddlers were injected with the 2nd dose, 98 toddler were injected with the 3rd dose, and only 21 toddlers (5%) made it to the 1-month post 3rd dose follow-up visit with the study doctor.

What Happened to 344 Babies Who Were 6 to 23 Months Old?

In an unblinded placebo subgroup of 377 babies 6 to 23 months old, 344 babies were injected with the 1st dose of 3μg of mRNA nanoparticles, 296 babies were injected with the 2nd mRNA dose, 77 babies were injected with the 3rd mRNA dose, and only 3 babies (1%) made it to their 1-month post 3rd mRNA dose follow-up visit with the study doctor.

What Happened to the Babies and Toddlers?

Reasons for discontinuing or withdrawing from the study included (but need not be noted) included; adverse events, neurological dysfunction, ICU admission, hospitalization and death.

Other reasons include participation request (i.e. parent removing their child from the trial due to permanent disabling injuries or death) or an investigator removing a baby or toddler from the trial due to permanent disabilities or death.

The clinical trial design submitted by Pfizer to the FDA in the IND (initial new drug application) was not in compliance with laws that regulate the biologics industry (21 USC) and therefore were criminal experimentations on human adults and children. I just described 690 babies and infants who never made it to their 2-month follow-up visit with the investigational doctor. There was a total of 3,102 babies and toddlers who never made it to their 2-month follow-up visit. What happened to their babies?

Pray for Justice

My heart is saddened to think about what happened. I can’t imagine the pain these parents must be suffering. Pfizer is liable for the disease, disabilities, and death that they have inflicted on their babies and Pfizer is liable for the suffering they inflicted on millions of American adults, teenagers, children, toddlers, and babies.

Pray for justice.

Mark 9:42

“But whoever causes one of these little ones who believe in Me to stumble, it would be better for him if a millstone were hung around his neck, and he were thrown into the sea.”