Robin Monotti ( + Cory Morningstar )
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Forwarded from Eshani King
Moderna's own 2012 research shows LNPs end up in your brain and in fact everywhere. Potential in brain to cause autoimmune reactions, inflammation and cause protein mis-folding (dementia/Alzheimer's risk?). Potential to impact gametes in reproductive organs.

https://thehighwire.com/videos/neuroscientists-concerns-about-covid-vaccines/
Pfizer & BioNTech Update, "6 Month Safety and Efficacy Data Analysis of Landmark COVID-19 Vaccine Study" JULY 28, 2021—

"Available data on #Pfizer-BioNTech COVID-19 Vaccine administered to #pregnant women are insufficient to inform vaccine-associated risks in pregnancy" [p 4]
Forwarded from DISASTER X (Maximilian Forte)
August 23, 2021 Approval Letter - Comirnaty.pdf
160.7 KB
Sent to me by colleagues, please examine this FDA letter to Pfizer—it lists the many safety studies yet to be undertaken by Pfizer, and in some cases the completion dates for these studies are in 2025. The list of safety studies to be undertaken begins on page 5, and consists of 13 individual studies.

#covid19 #FDA #Pfizer
Forwarded from DISASTER X (Maximilian Forte)
Forwarded from DISASTER X (Maximilian Forte)
Disclosing Pfizer vaccine data ‘may take until 2096’
[Memo from the year 3096: still not done releasing documents]

EXTRACT:
The US Food and Drug Administration is cooperating with a Freedom of Information Act request for clinical data associated with Pfizer’s Covid-19 vaccine, but may require 75 years to do so – even longer than a prior estimate.

The FDA has insisted it cannot commit to a faster release of the medical data associated with the approval of the Pfizer-BioNTech coronavirus vaccine, according to a legal brief filed on Tuesday in response to the FOIA request. The agency reiterated that after processing 12,000 pages in about a two-month period, it will only be able to process 500 pages per month going forward. With tens of thousands of additional files up for review, plaintiffs fear the process may drag on two decades longer than the previous 55-year estimate.

Lawyer Aaron Siri sued the FDA on behalf of a group of doctors calling themselves Public Health and Medical Professionals for Transparency, who had previously complained the FDA wasn’t supplying the data they had requested in a timely fashion. Having pointed out last month that the FDA had looked through Pfizer’s documents in a mere 108 days in order to license the vaccine, Siri questioned why the agency now required a whopping 20,000 days to make the same documents public.

CONTINUE HERE:
https://www.rt.com/usa/542616-fda-years-declassify-pfizer/

#covid19 #Pfizer #FDA #secrecy
Informed Consent

Nov 19 2021: authorization of #Pfizer Comirnaty extends to children 5-11 yrs.

Deaths WITH Covid as of Nov 12, 2021:

Age 0-19: 17

"SERIOUS" adverse events reported/accepted as of Jan 14, 2022:

Age 12-17: 291

The "benefits" do not outweigh the risks (risk nearing 0).

[Morningstar, Twitter]
Forwarded from DISASTER X (Maximilian Forte)
Pfizer’s Own Informed Consent Documents Undermine FDA and CDC’s Cries of “Safe and Effective”

EXTRACT:
Pfizer’s own informed consent documents, recently obtained by ICAN, show it discloses potential concerns, including myocarditis, original antigenic sin, and birth defects, while the FDA & CDC whitewash these concerns to declare these products are safe and effective.

ICAN has now obtained the materials used by the Cincinnati’s Children’s Hospital in conducting its studies of the Pfizer booster vaccine, including in children. The documents prepared in consultation with Pfizer tell us a lot about how Pfizer understands the risks of its products.

Pfizer is clearly worried about the risks of myocarditis (heart inflammation) in kids. Pfizer’s own informed consent documents reveal that the risk of myocarditis may be as high as 1 in 1,000 (see page 4).

But the FDA and CDC blithely ignored this risk in approving the Pfizer mRNA shot in kids. Only after rushing this product through the approval process did the CDC begrudgingly admit that “Myocarditis and pericarditis have rarely been reported, especially in adolescents and young adult males within several days after COVID-19 vaccination.”

Pfizer is also aware of the possibility of original antigenic sin and pathogenic priming (unwanted immune responses that leave one worse off in response to a virus than if one had done nothing). Pfizer warns parents of clinical trial participants that “it cannot yet be ruled out that the study vaccine could make a later COVID-19 illness more severe” (emphasis added). The FDA and CDC go to great lengths to hide that information while proclaiming “safe and effective” over and over again like a mantra.

Pfizer appears very worried about the potential of the teratogenesis (harm to a developing fetus) and even possibly mutagenesis (harm to DNA). So even though this is a trial in children, Pfizer disclosed to the parents of these children that “the effects of the COVID-19 vaccine on sperm, a pregnancy, a fetus, or a nursing child are not known.”

But then Pfizer goes even further to state that:

—“If your daughter is pregnant, planning to become pregnant or is breast feeding a baby, she cannot be in the study as there may be risks to the unborn baby or nursing baby.Nobody knows what these risks are right now.”

—“If your daughter becomes pregnant, she will have to leave the study.”

—“If your child is a boy, and he thinks he may have gotten a girl pregnant, he or you must tell your child’s study doctor immediately. The study doctor may ask for information about the pregnancy and the birth of the baby. The study doctor may share this information with others who are working on this study.”

—“If your son is taking part in this study, he is not allowed to donate sperm for at least 28 days after his last vaccination.”

Let’s just pause to acknowledge just how deeply unsettling this language is. But it just goes to show that Pfizer wanted to make sure that they had no data at all on pregnancy outcomes. ...

CONTINUE HERE:
https://www.icandecide.org/ican_press/pfizers-own-informed-consent-documents-undermine-fda-and-cdcs-cries-of-safe-and-effective/

#covid19 #Pfizer #informed_consent #ethics #vaccine_dangers
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