Governor Tom Wolf via Flickr

This week, the Food and Drug Administration (FDA) may decide that COVID booster doses may be given to Americans prior to the conclusion of human research. Concerns regarding the new booster’s impending introduction are brought on by the utter lack of human studies. The FDA has been asked by Pfizer and BioNTech to approve an emergency use authorization for their COVID vaccine that has been modified to work with the BA.4/BA.5 versions of the Omicron variant. The urgent request would theoretically enable the approval of a booster without the customary research necessary for such a vaccine.

As The Daily Wire reports:

The new booster dose is intended for individuals 12 years of age and older and would be available to ship immediately, according to a news release from the company.

“The agility of the mRNA platform, together with extensive clinical experience with the Pfizer-BioNTech COVID-19 Vaccine, has allowed us to develop, test and manufacture updated, high-quality vaccines that align to circulating strains with unprecedented speed,” said Albert Bourla, Chairman and CEO of Pfizer.

“Having rapidly scaled up production, we are positioned to immediately begin distribution of the bivalent Omicron BA.4/BA.5 boosters, if authorized, to help protect individuals and families as we prepare for potential fall and winter surges,” he added.

The most recent data provided by the CDC reveals that the BA.5 variant is responsible for 88.7% of all new cases between August 21 and August 27. The BA.4 variant included an additional 3.6% of new cases.

Moderna has also asked the FDA for permission to use their upgraded COVID vaccine, which targets the most recent coronavirus strains in addition to Pfizer/BioNTech. If accepted, it might arrive in September. Moderna stated that it started the booster’s clinical testing earlier this month. The approval of an emergency usage does not require full human clinical trials.




Comments

  1. Here we go again – making Anmericans test specimens . Hopefully this won’t be mandated like the others and we have the choice to be part of their experiment or not

  2. Again, it seems Pharma will again “vaccinate” AFTER the threat from the new strains has passed! Probably nothing useful in the “vaccines” other than toxins.

  3. I have had a runny nose and cough ever since I took the first two. No more for me. From what I have surmised, they are just a money grab by the drug makers and a political ploy by politicians. They do not prevent any disease; they do not prevent the spread of covid.

    1. only those that have been dumbed down over the years into taking whatever the evil greedy Pharms put out

  4. No ones dying of Omicron and its no Pandemic, thus there is no need for EMERGENCY use Authorization and never was, since the Covid19 was a man made bio weapon used to facilitate the Injectable Covid 19 that does similar but slightly different damage. Its more DNA/RNA oriented

  5. I’m done with the vaccines. I’ve had 2 vaccines and 2 boosters and still got COVID. I’m now suffering from cardiac issues that came on suddenly and my cardiologist says is’s unusual for these symptoms to suddenly appear. I still don’t know what the issue is. Think long and hard before you get another shot. Especially one not fully tested.

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