https://davidicke.com/2021/02/01/dr...technology-all-animals-died-upon-reinfection/
In animal studies, after mRNA injections have been administered to cats, when the virus arrived once again into the body, it arrived like a Trojan Horse, undetected by the cats’ own immune system. The virus multiplied unchallenged and all animals involved in the experiment died from various causes.
According to Dr. Lee Merritt,
What happened is all animals died… but they didn’t died of the “vaccine”. What they died from what used to be called “immune enhancement” and now they call it “antibody dependent enhancement” (ADE).
https://www.nbcnews.com/health/heal...ew-covid-boosters-data-tests-people-rcna45387
Because the Biden administration has pushed for a fall booster campaign to begin in September, the mRNA vaccine-makers
Pfizer-BioNTech and
Moderna have
only had time to test the reformulated shots in mice, not people. That means the Food and Drug Administration is relying on the mice trial data — plus human trial results from a similar vaccine that targets the original omicron strain, called BA.1 — to evaluate the new shots, according to a recent
tweet from the FDA commissioner, Dr. Robert Califf.
That could be a potentially risky bet, experts say, if the shots don’t work as well as hoped.
But the lack of data in humans means officials likely won’t know how much better the new shots are — if at all — until the fall booster campaign is well underway.
The FDA’s decision to move forward without data from human trials is a gamble, experts say, threatening to further lower public trust in the vaccines should the new boosters not work as intended.
https://www.businessinsider.com/2-top-fda-officials-resigned-biden-booster-plan-reports-2021-9
The US Food and Drug Administration announced the resignations of two top vaccine officials on Tuesday, and reports said the two were leaving in anger over the Biden administration's plan to roll out COVID-19 booster shots before officials had a chance to approve it.
https://www.wsj.com/articles/fda-sh...er-covid-vaccine-pandemic-science-11649016728
The Food and Drug Administration last week authorized Americans 50 and over to get a fourth Covid vaccine dose.
Some of the FDA’s own experts disagree with the decision, but the agency simply ignored them.
https://www.nytimes.com/2021/09/24/world/covid-boosters-vaccine-cdc-director.html
The director of the Centers for Disease Control and Prevention on Friday
overruled a recommendation by an agency advisory panel that had refused to endorse
booster shots of the Pfizer-BioNTech
Covid vaccine for frontline workers. It was a highly unusual move for the director,
Dr. Rochelle Walensky, but aligned C.D.C. policy with the Food and Drug Administration’s endorsements over her own agency’s advisers.
https://www.fda.gov/emergency-prepa...-policy-framework/emergency-use-authorization
Under section 564 of the Federal Food, Drug, and Cosmetic Act
(FD&C Act), when the Secretary of HHS declares that an emergency use authorization is appropriate, FDA may authorize unapproved medical products or unapproved uses of approved medical products to be used in an emergency to diagnose, treat, or prevent serious or life-threatening diseases or conditions caused by CBRN threat agents when certain criteria are met, including there are no adequate, approved, and available alternatives.
The HHS Secretary has issued several Declarations pursuant to section 319F-3 of the PHS Act to provide
liability immunity for activities related to medical countermeasures against COVID-19.
...
