From Joseph Mercola, DO
The COVID jabs have been the deadliest medicine in history, but could these reformulated shots be even worse? They’ve been tested on just eight mice; now parents are going to be encouraged to give it to their babies. What could possibly go wrong?
With their authorization of reformulated COVID mRNA boosters without the standard steps of testing, the U.S. Food and Drug Administration and the Centers for Disease Control and Prevention have completely abandoned science. They’re both simply rubber stamping whatever the drug industry wants to do, without any concern for public health whatsoever.
August 31, 2022, the FDA authorized the reformulated shots, and they didn’t even allow members of its Vaccines and Related Biological Products Advisory Committee (VRBPAC) to meet, discuss or vote on the matter.
Instead, they pushed the matter before the CDC’s Advisory Committee on Immunization Practices (ACIP). ACIP met for eight hours September 1, 2022, and authorized the untested boosters 13-to-1. CDC director Rochelle Walensky endorsed the recommendation later that evening.
As reported by Yahoo! News:
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 …
That could be a potentially risky bet, experts say, if the shots don’t work as well as hoped … 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.