by Brian Shilhavy
Editor, Health Impact News

After an FDA Advisory Committee voted 20 to 0 with one abstention to issue Moderna emergency use authorization (EUA) for their mRNA experimental COVID vaccine, the FDA took their advice today and issued the EUA.

As is the case with the Pfizer mRNA experimental vaccine which received an EUA last week, it is important to understand that this vaccine is NOT approved by the FDA.

It is only authorized to be used in emergency situations, and the Health Bureaucrats who make these decisions for everyone have already planned to make COVID an “emergency pandemic” that apparently will last for more than a year, if not longer.

The Advisory Committee that met on Thursday, much like the same Advisory Committee that met last week to give the go-ahead to the Pfizer experimental mRNA COVID vaccine, is entirely comprised of pharmaceutical industry insiders, such as Paul Offit of The Children’s Hospital of Philadelphia who himself is a patent holder of a vaccine in the CDC Childhood Vaccine schedule that earns him millions and once claimed that an infant can easily receive 10,000 vaccines at one time, and Paula Annunziato, a top executive for Merck pharmaceutical company, a major producer of vaccines. (Source.)

The sole abstention came from Michael Kurilla, who works for the National Institute of Health. He stated:

“I abstained because I am uncomfortable with the language. In the midst of a pandemic and with limited vaccine supply available, a blanket statement for individuals 18 and older is just too broad. I’m not convinced that for all of those age groups that the benefits do outweigh the risks. I want to see it more targeted toward people at high risk of serious and life-threatening COVID-19 disease.” (Source.)

The other concern that was allegedly discussed was the fact that three of the trial participants contracted Bell’s palsy, which causes paralysis in the face. The trial group also saw 13 deaths, 6 in the vaccine group, and 7 in the placebo group. There were only 6 deaths total in the Pfizer trials.

Nevertheless, the only thing they were voting on for emergency use authorization, was whether or not the potential benefits of the vaccine out-weighed the risks, and not whether or not people were going to be injured and killed by the vaccine, as that just seems to be an acceptable side effect.

With the vaccine not going through the full approval process, an EUA allows the pharmaceutical company to complete their trials in the public at large, using Americans basically as lab rats to complete their study and try to gain full approval.

COVID Experimental mRNA Vaccines Issued EUAs are Illegal

As we reported on the Pfizer experimental vaccine, there are legal requirements for the FDA to authorize an unapproved drug or vaccine for emergency use. One of those requirements is that there cannot be any other approved drugs or vaccines in the market that already work.

With COVID19, tens of thousands of doctors worldwide have testified to the fact that there are at least two safe drugs already in the market and approved by the FDA that have been used successfully, often with a 100% success rate, to treat patients diagnosed with COVID19.

Those drugs are Hydroxychloroquine, and Ivermectin.

Another reason why the FDA’s authorization of the experimental Pfizer COVID vaccine is illegal, is that the clinical trials used to justify its emergency use authorization, used the faulty PCR COVID test to determine if the clinical trial patients had COVID19 or not.

Dr. Sin Hang Lee, a world-renowned expert on DNA sequencing-based diagnostics, filed an ADMINISTRATIVE STAY OF ACTION with the FDA prior to the FDA issuing emergency use authorization to Pfizer and Moderna, stating that their testing was faulty, and that more reliable testing was needed before these vaccines were used in the public. See:

“Stay of Action” Filed Against FDA to STOP Approval of COVID Vaccine for Using Faulty PCR Tests in Trials

The FDA ignored this Stay of Action.


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