It’s true. According to a recent risk-benefit analysis it will cause 18-98 serious adverse events for each hospitalization it prevents, yet Biden just ordered 171M doses based on a study of 8 mice …
STORY AT-A-GLANCE The emergency authorizations of Pfizer’s and Moderna’s bivalent COVID boosters are based on preliminary test results from a grand total of eight mice, and that data hasn’t even been made public
Based on the antibody response in eight mice, the Biden administration has ordered 171 million doses of the two boosters
A reanalysis of data from the Pfizer and Moderna COVID vaccine trials found that, combined, the jabs were associated with a risk increase of serious adverse events of special interest at a rate of 12.5 per 10,000 vaccinated. Meanwhile, the risk reduction for COVID-19 hospitalization was only 2.3 per 10,000 participants for Pfizer and 6.4 per 10,000 for Moderna
According to a recent risk-benefit analysis of a third booster for university students, for each COVID hospitalization prevented, the booster will cause 18 to 98 serious adverse events
A number of top officials with the FDA, CDC and the NIH reportedly have serious concerns about the direction we’re going in, yet are too afraid to speak out or push back August 31, 2022, the U.S. Food and Drug Administration authorized the reformulated COVID bivalent booster shots by Moderna and Pfizer1 — all without the required convening of its Vaccines and Related Biological Products Advisory Committee (VRBPAC), which would typically discuss or vote on the authorization or approval of a new vaccine….