EFFICACY is again the problem......there are NOT enough effective,efficient and LARGE trials being looked at.....JMO. The data should have been more CLEAR AND CONCISE. I'm a not a scientist,BUT IT IS APPARENT, there is NO CONSENSUS about the real longevity of product (J&J came out ahead of the pack,is it because of their methods?)
Why anyone would give an experimental shot to a toddler who has almost zero chance of serious illness is beyond me. How could you possibly trust a mixture of chemicals that had no long term testing? Probably the same people who are still masked up in their cars.
The left is angry because they are now being judged by the content of their character and not by the color of their skin.
I find it disconcerting that the "vaccine" is being released under the Emergency Use Authorization process. Where is emergency regarding Covid infections in toddlers?
Also in my readings I could not find any source that indicates when an EUA expires. Does anyone have information that would answer the question?
How will vaccine recipients be informed about the benefits and risks of any vaccine that receives an EUA?
FDA must ensure that recipients of the vaccine under an EUA are informed, to the extent practicable given the applicable circumstances, that FDA has authorized the emergency use of the vaccine, of the known and potential benefits and risks, the extent to which such benefits and risks are unknown, that they have the option to accept or refuse the vaccine, and of any available alternatives to the product. Typically, this information is communicated in a patient “fact sheet.” The FDA posts these fact sheets on our website.
U R SO FUNNY.......
