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More vaccine mandates may be imposed across the US once the Food and Drug Administration gives its final stamp of approval to COVID-19 shots, health experts have predicted.
The three vaccines on the market are currently being administered under an emergency use authorization but a full regulatory sign off could remove legal hurdles for businesses and government agencies that want to require shots for their customers and employees, NBC News reported.
Full approval is the FDA’s strongest endorsement of a drug and typically requires six months of safety follow-up.
Pfizer and Moderna have applied for full approval of their two-dose vaccines, both of which secured emergency use authorization in December.
The US Food and Drug Administration (FDA) has added a warning about the risk of heart inflammation to fact sheets for Moderna and Pfizer-BioNTech COVID-19 vaccines. The warning on Friday noted that reports of adverse events following vaccination – particularly after the second dose – suggest increased risks of myocarditis, or inflammation of the heart muscle, and pericarditis, or inflammation of the tissue surrounding the heart.
originally posted by: OccamsRazor04
a reply to: HawkEyi
I was told it's not a vaccine and will never get approved because millions will be flooding the hospitals and everyone will be sterile and magnetic.
Once approved will it still 'not be a vax'? Your OP is full of opinion, I don't see much in the way of facts or data. I would like more info on the risks, how many cases, how many vaccines administered.