Why are there 23 babies suffering adverse events in the context of the 'bivalent' shots? - 35% as first doses

There really are no rules anymore, are there.

VAERS ID: 2464492

→ SYMPTOM_TEXT: “Bivalent Pfizer given to 4 year old patient not approved for emergency use at this age group. Only approved for 12 and over.”

By the way, this 4 year old child is also reported to have following pre-existing conditions

→ CUR_ILL: “Speech Delay, Developmental delay Autism spectrum disorder Vascular ring with right aortic arch and left arterial ligament with anomalous retroesophageal left subclavian artery”.

Should this child be injected with anything at all, let alone this unapproved experimental product?

CDC's Director Rochelle P. Walensky approved the use of the vaccine for children ages 5 though 11 on Wednesday, according to the CDC. 

The bivalent booster vaccine is referred to as an updated booster and is used to combat the omicron variant of COVID-19. It was originally made available for people of ages 12 and older on Sept. 2, [2022] according to the agency.¹

So if this is the case, then why the hell are there 23 adverse event reports in VAERS for babies ages 0-4?

Clinical trial research submitted to the FDA found that the side effects of the booster are similar to that of the other COVID-19 vaccines. These common symptoms are pain, redness and swelling at the injection site, fatigue, headache, muscle pain, chills, nausea/vomiting and fever.

These symptoms were reported by a clinical study of 800 participants ages 18 and older. There is currently no research on how the bivalent vaccine will effect people ages 12-17.

Ohohohoohooo! 800 whole young adults! Wow! That’s almost as good as 8 mice!

Once again, there is NO SAFETY DATA for 5-11 year olds or for 12-17 year olds. There is certainly no safety data for babies.

Let’s take a look at what adverse events are being reported to VAERS for the babies ages 0-4 (N total = 23; left) and for the 5-11 year olds (N total = 42; right).

These bar charts only show the adverse events from SYMPTOM1 column since this is the most populated variable. There are 4 other SYMPTOM variables where Vomiting, Sensory loss and Hand-foot-and-mouth disease are also listed as adverse events. Why the hell are we injecting babies with an experimental product that was tested on 8 mice?

I just have no words.

I want an explanation Walensky. I think the parents of these babies and children are owed one as well.

N.B.: VAERS ID 2447829 possibly has their age documented incorrectly in VAERS - it is documented as 0.25 years and since there are concurrent reports of chest pain and electrocardiogram (“15 minutes after patient received her Covid Booster she complained of chest pain”), it is more likely this person is not 0.25 years old. So to be fair, there are likely 22 babies with reports filed to VAERS as of October 14, 2022 in the context of the ‘bivalent’ shots, rather than 23. This does not include an URF.

1. http://www.nicholsonstudentmedia.com/news/more-covid-19-protection-cdc-makes-bivalent-vaccine-available-for-most-age-groups/article_9c52d018-466b-11ed-9850-3b387a3968fd.html