I just don’t know quite what to say about this. Perhaps what I would like to ask is this: who are the pediatricians and mothers of these infants and why are they injecting them with these products? These are the ‘safe’ products on the childhood vaccination regimen? Really? There are currently (as of December 31, 2021) N = 25,754 adverse event reports in VAERS in the Domestic and Foreign data sets for babies aged 0-2. If we use the Under Reporting Factor of 41, this becomes 1,055,914. That’s a big number.
By Jessica Rose
I decided to look into this because I did a podcast with James, Mathew and Geert last night (January 3rd, 2021) and I stated that there are hundreds of reports for babies in VAERS and wondered out loud how that could be. So I checked the exact number today among all vaccines for the most recent VAERS data download.
Fact #1: Did you know that 99.4% of the bloody reports are ‘hidden’ in the Foreign data set?
When the Domestic and Foreign data reports for 0-2 year olds from VAERS are plotted against the difference in the time between the injections and the onset of the adverse events (AEs), we see that a little more 50% are made immediately and 70% are made within 24 hours.
There are many different types of adverse events made for babies aged 0-2. These adverse events include the following in order of descending frequency. 613 of these babies died from various vaccines/products in 2020/2021. Listed below are the top adverse event reports for SYMPTOM1 column only. There are 5 SYMPTOM columns.
What of the COVID-19 products?
If we put a filter on the product manufacturer for COVID-19, the N decreases significantly to N = 244. The distribution of the events can be seen in the figure below.
Fact #2: 5 babies have died in temporal proximity of the COVID-19 products – 4 in association with Pfizer and 1 in association with Moderna.
- 958443 (within 2 days – Pfizer)
- 1166062 (within 1 day – Pfizer)
- 1261766 (within 2 days – Moderna)
- 1659812 (within 0 days- Pfizer)
- 1720648 (within 7 days – Pfizer)
We can also assess the percentage of adverse events reported within close temporal proximity to the injection date.
I wanted to simply document this today. I have no message.
