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 1. Blaze Media /
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HOROWITZ: MODERNA PUSHING HIGH-DOSE SHOT FOR BABIES WHO ARE IN NO DANGER FROM
COVID

Op-ed

Daniel Horowitz
March 28, 2022


Miyer Juana Long/Getty Images

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Would red-state governors tolerate a federally funded program to distribute
abortifacients in their states? Well, these same governors need to make it clear
that Pfizer and Moderna are the new Planned Parenthood and are not welcome to
distribute their poison shots in their states, especially for babies.

The pandemic has basically been declared over, babies and toddlers were never in
danger, the shots no longer work, and they have been proven devastating in
adverse events, even with the amount of long-term consequences we see. Yet both
Pfizer and Moderna are in the process of senselessly and cruelly targeting the
youngest children for the COVID shots. However, there is something particularly
concerning about Moderna’s shot, in that the company is proposing to use a
25-milligram dose on babies 6 months to 2 years old, more than eight times the
dose of Pfizer’s baby shot!



We are talking about kids weighing 15-25 pounds, and they are giving a dose that
is almost as big as Pfizer’s adult dose. It’s one-fourth the dosage of Moderna’s
adult dose, but that is still a much greater concentration for an average
6-month baby than it is for an adult of 160 pounds. How could anyone think this
is safe?



Don't miss out on content from Dave Rubin free of big tech censorship. Listen to
The Rubin Report now.



Here’s what is really going on. All of the Pfizer and Moderna studies even for
older children have shown zero serious COVID cases in the respective placebo
groups. So in order to show efficacy, they created arbitrary benchmarks for
presence of specific antibody levels generated by the shots. Putting aside the
fact that high antibody levels without the proper T cell responses are actually
not a good thing, fail to provide sterilizing immunity, and potentially cause
autoimmune problems, the drug companies are caught in a catch-22 with dosage.
Pfizer rightly tested those under 5 years old with a 3-milligram dose. But then
it failed to stimulate a proper antibody response, which is why the company had
to temporarily withdraw its application for EUA.

Moderna, on the other hand, figured they’d solve the problem by giving babies
and toddlers a whopping 25-milligram dose. Even then, they misleadingly tethered
their study of 2- to 4-year-olds to 5- and 6-year-olds in order to even register
this illusory efficacy. However, any sane person on the FDA advisory committee
should automatically nix this shot on account of its dangerous concentration for
babies who, at just 6 months, average (for girls) as light as 16 pounds. Thus,
while a 20-year-old adult weighing 180 pounds could be getting 0.55 micrograms
per pound with the 100-microgram dose, a 6-month-old baby could be getting more
than 1.5 micrograms per pound, roughly three times as potent. And we already
know how problematic the adult concentration of Moderna was for many young
adults, especially related to cardiac issues.

Then again, the entire premise of approving this shot at any dose for babies is
taking a chapter out of Josef Mengele’s book of human experiments. By
definition, there is zero emergency now, and even at the peak of the pandemic,
there was no emergency for young children. There was, by definition, zero
efficacy against serious illness, and they claim 37%-43% efficacy against
infection for the various age groups. However, what are the consequences of
getting an infection if it’s not serious? They report 17% of the kids got fever
from the shots! So you are giving them fever and something that can induce
several thousand ailments and maladies long-term (with no long-term safety data)
for the 40% chance of … avoiding fever from the virus!

Also, the FDA plainly stated (p. 10) that “a point estimate for a placebo
controlled efficacy trial of at least 50%” must be demonstrated in the trial in
order to receive emergency use authorization. Moderna’s own untransparent data
demonstrates the shot has not met the threshold for consideration



But that’s assuming you believe the 40% efficacy the way you believed the 90%+
efficacy against the original strain in the first adult studies. Now, if you
believe there is still even a 40% VE rate against Omicron, especially against
infection, after every single country-based analysis of real-world data showed
negative efficacy since the beginning of Omicron (and U.K. data showed it even
in Delta), I have a biolab to sell you in Wuhan. According to the U.K. Health
Security Agency’s most recent report, efficacy against infection for some age
groups is now lower than -300%.


But let’s play Charlie Brown in the football game with Lucy for a moment and
assume that this time, they are telling the truth about 37%-43% efficacy against
infection. Even the most conservative estimates of the adverse events from
thousands of maladies detailed in Pfizer’s own document now released via FOIA
demonstrate how it is immoral to market this to any child. Moderna has failed to
disclose the number and types of adverse events. What it did divulge, however,
is concerning. “The majority of adverse events were mild or moderate and were
more frequently reported after dose two,” read the press release. The majority
were mild or moderate, which means that a good number of them could have been
significant. It also means that a minority but still measurable number of the
adverse events were severe. How many and what type? They don’t say.

Remember how a number of countries banned Moderna’s shot for those under 30
because it caused exponentially more myocarditis than even Pfizer, presumably
because of the higher dose? Iceland completely banned it. And this is when the
shot was alleged to be more effective and for older strains of the virus. Now,
they are using an expired shot for babies at a massive dose – much greater per
pound – knowing the cardiac issues. Moreover, Moderna has been even less
transparent than Pfizer, so we don’t even have its list of known adverse events
the company is undoubtedly quietly monitoring. This is no longer malpractice but
downright Third Reich-level malfeasance.

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developing and adopting new technologies. All this is meant to reach the optimal
level of accessibility following technological advancements. If you wish to
contact the website’s owner, please use the website's form

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