22 November 2022 (13:13-UTC-07 Tango 06) 01 Azar 1401/27 Rabi ‘ath-Thani 1444/29 Xin-Hai 4720/22 ноября 2022 года
On 12OCT2022, the U.S. Food and Drug Administration (FDA) pronounced revised “emergency use authorizations” (remember, that is not the same as being fully approved) for the Moderna and the Pfizer-BioNTech Bivalent Pandemic vaccine boosters, allowing for their (what in effect is experimental) use in children.
On 16NOV2022, the U.S. Army, in Europe, proudly announced they had already begun issuing the so-called immunization booster for adults, and were now ready for children.
In this U.S. Army (USA) Europe video, notice they are careful to use qualifiers like “estimated” (unlike the U.S. Navy which outright lies and claims the emergency use designation is the same as being approved), however, the USA doctor does lie by making the yet-to-be-scientifically-proven statement that the bivalent booster “offers broader protection spectrum than any previous vaccine or booster”:
In regards to emergency use versus approval, the FDA states “Under section 564 of the Federal Food, Drug, and Cosmetic Act (FD&C Act), when the Secretary of HHS declares that an emergency use authorization is appropriate, FDA may authorize unapproved medical products or unapproved uses of approved medical products to be used in an emergency to diagnose, treat, or prevent serious or life-threatening diseases or conditions caused by CBRN threat agents when certain criteria are met, including there are no adequate, approved, and available alternatives.” Please notice the repeated use of the word ‘unapproved’, and the statement that emergency use is authorized when “there are no…approved….alternatives” !
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