The U.S. Food and Drug Administration (FDA) just announced that approval has been granted for Moderna’s “Spikevax” injection, which they are calling a “vaccine.”
All this time, Spikevax has not had FDA approval, but rather an “emergency use authorization” (EUA) allowing it to be administered at warp speed without the proper trials. Now, Spikevax has the FDA’s official blessing.
“Our COVID-19 vaccine has been administered to hundreds of millions of people around the world, protecting people from COVID-19 infection, hospitalization and death,” announced Stéphane Bancel, Moderna’s CEO, in an announcement.
“The totality of real-world data and the full BLA for Spikevax in the United States reaffirms the importance of vaccination against this virus. This is a momentous milestone in Moderna’s history as it is our first product to achieve licensure in the U.S.”
Bancel added that Spikevax is already approved in Canada, Japan, the European Union, the United Kingdom, Israel and several other countries “where the adolescent indication is also approved.”
“We are grateful to the U.S. FDA for their thorough review of our application,” he went on to state. “We are humbled by the role that Spikevax is playing to help end this pandemic.”
FDA relied on data supplied by Moderna – not independent data – to grant approval for its vaccine
Speaking of Japan, the Ministry of Health in that country issued a warning back in the summer about how Moderna’s jab vial contain mysterious “black substances.”
Metallic particles that some suspect might be graphene oxide were detected inside the vials, prompting the Japanese government to suspend some of the 1.6 million doses that were available there at the time.
“We are suspending the use of Moderna Covid-19 vaccines as foreign substances were spotted,” authorities in Okinawa announced at the time, suggesting the affected batches might be dangerous.
Bancel, of course, made no mention about these particles in his statement suggesting that Japan and other nations are happy with his company’s injections.
The FDA claims that it based its approval decision on “the totality of scientific evidence shares by [Moderna] in its submission package.” All of this “scientific” data showed “high efficacy and favorable safety,” of course, seeing as how it was manufactured by the company.
Regulators in more than 70 other countries also relied on the same “scientific data” to grant their approval as well. This proves that it is not just the FDA that is corrupt, but also many other government agencies that have also been infiltrated.
Since Dec. 18, 2020, when Donald Trump was still in office, Moderna has had EUA for its mRNA (messenger RNA) vaccine. Trump bragged about the shot being “safe and effective” as he introduced it under Operation Warp Speed along with Pfizer’s mRNA jab and the viral vector jab from Johnson & Johnson (Janssen).
“Under an EUA, the FDA has the authority to allow medical products to be used in an emergency to diagnose, treat, or prevent serious or life-threatening diseases or conditions during a declared public health emergency when there are no adequate, approved, and available alternatives,” Moderna said in a news release.
“A booster dose of the Moderna COVID-19 vaccine at the 50 µg dose level is authorized for emergency use in the U.S. under EUA for adults 18 years and older. A third dose of the Moderna COVID-19 vaccine at the 100 µg dose level is authorized for emergency use in immunocompromised individuals 18 years of age or older in the United States who have undergone solid organ transplantation, or who are diagnosed with conditions that are considered to have an equivalent level of immunocompromise.”
More of the latest news about Wuhan coronavirus (Covid-19) “vaccines” can be found at ChemicalViolence.com.
(Article by Ethan Huff republished from NaturalNews.com)
