11/02/2022 / By Lance D Johnson
In August of 2021, the Centers for Disease Control (CDC) pressured regulators at the Food and Drug Administration (FDA) to approve the first covid booster shot for Pfizer and Moderna WITHOUT clinical trials. The coercion took place even though the CDC was fully aware that “fully vaccinated” patients were filling up the ICUs.
According to a Freedom of Information Act (FOIA) request filed by Judicial Watch, the government’s internal emails show blatant collusion, coercion, and medical fraud occurring between the federal agencies. The emails show that there was a complete disregard for vaccine safety and efficacy at the highest levels of government. The agencies also admitted yet ignored evidence that the “fully vaccinated” were filling up ICUs.
While the emails are mostly redacted, there is enough written correspondence to show that CDC officials wanted to force out vaccines on the population, without any clinical trials and even while the data showed that the vaccines weren’t working as initially propagated.
In a conference call with other members of the FDA, Dr. Phil Krause, a top FDA official, described a conversation he previously had with CDC officials. “Take a deep breath before reading this next paragraph. On that call, the CDC evidently stated that they will assemble all the data they are aware of on third dosing in this setting and send it to us in the hope that we will (very soon) authorize the third dose for immunocompromised as part of the EUA,” Krause wrote in the Aug. 5, 2021, email.
At that time, all the covid-19 vaccines were authorized under the FDA’s emergency use authorization (EUA). At the time, there was tremendous political pressure to submit the entire population to the experimental vaccines as a precondition to opening up states, schools, and industry. Dr. Krause wrote in an email, “But it doesn’t sound like they [CDC] actually want to do a study. They just want to vaccinate these people—if I am reading this correctly.
Dr. Jay Bhattacharya, a professor of medicine at Stanford University wrote on Twitter that the emails do show “the CDC wanted the booster approved without a trial.”
Dr. Richard Nathan wrote to the FDA, pushing for boosters because Israel had done it and Pfizer recommends more dosing. “Pfizer recommends it and I trust their guidance over the turmoil at our federal agencies. With millions of doses of vaccine set to expire, you should do what you think is best for your patients,” Dr. Nathan wrote. “I can’t believe you would get pushback from anyone,” he said to Doran Fink, who works for the FDA’s Center for Biologics Evaluation and Research. “Keep in mind, nearly everyone in this group is six to seven months out from the second dose of the vaccine and many have significant daily exposure to the virus.” Dr. Nathan pressured.
Doran Fink, said Dr. Nathan’s post “accurately reflects more widespread thinking that I am hearing in other forums as well,” including doctors who advise the CDC on vaccines.
Another pressure was recorded in a highly redacted email to Dr. Helen Gemignani at the FDA. The email read, “We currently have a few immune compromised patients in our ICU who were fully vaccinated. It is difficult to remain patient when we are on the front lines observing this happen. We would like to initiate a third dose boost as soon as possible on our most vulnerable patients. Is there a way to expedite this request?”
“Providers are losing confidence in FDA/CDC to do the right thing for their patients,” Fink said in her emails. Just two weeks later, the FDA said they conducted “a thorough review of the available data” while authorizing covid-19 boosters for “immunocompromised persons” – even though there were NO completed trials by Pfizer or Moderna.
During the fiasco, Dr. Marion Gruber wrote to Dr. Peter Marks, a top FDA official: “We need to be given time to consider their data and cannot be pushed by these companies and, for that matter the Administration, who try to impose timeless [sic] that make no sense.”
By September of 2021, the FDA’s top official, Dr. Janet Woodcock, and the CDC’s top official, Dr. Rochelle Walensky, made a joint statement, claiming that boosters will be needed for all Americans to “maximize vaccine-induced protection and prolong its durability.” This medical fraud led to the resigning of Dr. Phil Krause and Dr. Marion Gruber, the two most honest FDA officials who pushed back against the fraudulent vaccine approvals.
With Krause and Gruber out of the way, the CDC and FDA began to approve more untested boosters on an ailing, dying, overly-vaccinated population. The disastrous covid-19 vaccine program and its trail of booster fraud continues to run amok over one year later.
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