The FDA Just Delayed Moderna For A Very Serious Reason!
As we enter a new phase of Biden’s vaccination mandate wherein teens need to be vaxxed, more reports are coming in that vaccines like Moderda has a very serious side effect among teenagers.
We know that science behind the vaccines is not yet perfected, it’s a known FACT – so is the side effects. I mean, should we allow our kids to put in trial with these vaccines?
The COVID-19 virus outbreak has destroyed many economies around the world, the U.S is not exempted. It also taken many lives and create a wall between the vaccinated and the unvaccinated people. Radicalism in another form.
And recently, FDA has made a breaking news to delayed approval for the Moderna vaccine for children for they have seen a very serious side effects.
According to the VAERS tracking website, in the United States, 4,144 Americans have died following the Moderna COVID vaccination. 11,346 have died due to the Pfizer vaccination.
Excerpt from The Examiner reports:
The U.S. Food and Drug Administration announced Friday it would delay its decision on the administration of the Moderna vaccine to adolescents, citing concerns the shot may lead to a heightened risk of a rare heart condition.
The FDA has not yet determined if the risk is higher for adolescents, but the agency is planning to review the data further before extending the vaccine’s eligibility, according to the Wall Street Journal.
“I think people can be reassured that the risk of myocarditis with an mRNA vaccine is low, it appears to be balanced between the different products,” Paul Burton, Moderna’s chief medical officer, told the outlet.
Previously, Sweden and Denmark have announced that they halted Moderna COVID vaccines for those under 30-years-old due to possible side effects.
Sources: The Gateway Pundit, The Examiner