German company BioNTech GmbH "biologics license application" for COMIRNATY was approved by FDA today August 23, 2021.
Company website:
https://biontech.de/
The Pfizer-BioNTech vaccine uses according to the FDA "the same formulation" as the "comirnaty" just approved, yet the FDA didn't approve Pfizer-BioNTech vaccine, only the biologics license submitted by the German company.
https://www.fda.gov/media/150386/download
There's more. The EUA was revised AND the "comirnaty" mRNA vaccine license was just approved.
What isn't approved by the FDA is the Pfizer-BioNTech vaccine.
Question:
Why would the FDA approve the biologics license application of a vaccine manufactured by a German company BioNTech GmbH, for full authorized 'interstate commercial use', but they won't approve the Pfizer-BioNTech vaccine that 'uses the same formulation'?
Soros has Antifa in the US to stop large gatherings by violence and criminal threats.
Fake News already rolling in.
The FDA did not approve Pfizer, they approved BioNTech GmbH.
The release today instructs the Pfizer vaccine products to show "This product is not approved or licensed by FDA"
No, the Pdozer-BioNTech GmbHvaccine is under EUA.
The BioNTech GmbH vaccine was just approved for full use in people 16 and older.
Correct.
The oath is to DO no wrong.
That does not include refusing to treat.
I don't like it either, but the hippocratic oath was not meant to force doctors to treat anyone. Forced labor is slavery.
FDA approval means nothing to me.
The FDA approved Quaaludes, which are now considered a Schedule 1 drug like heroin.
The FDA approved DES, a "synthetic form of estrogen, was marketed to the expecting mother who preferred to have a healthy baby. It claimed to prevent spontaneous abortion, miscarriage, and premature labor. Studies soon showed that mothers who took DES during the first five months of pregnancy were more likely to suffer from complications with their reproductive systems. The FDA finally banned it in 1971."
The FDA approved Vioxx, "an anti-inflammatory medication intended to treat arthritis, was the subject of one of the largest recalls in history. After it was approved in 1999, it was prescribed to over 20 million people and was one of the most widely prescribed drugs of 2003. The following year, it was recalled. One of the FDA’s own scientists, Dr. David Graham, estimated that Vioxx had been associated with more than 27,000 heart attacks or deaths linked to cardiac problems."