ADVERTISEMENT

Pfizer MUST release the ingredients list of their vaxx to the FDA BY 6SEP2021... 2 of the FDA’s most senior vaccine leaders just quit...

WVU82

Hall of Famer
May 29, 2001
179,814
52,330
718
“If Pfizer has not been honest with the American People and the FDA in regards to what’s in these vials, they have 14 days to come clean.”

She believes that the inconsistency of the adverse events (myocarditis, clotting, miscarriages, central nervous system disorders, magnetization, etc.) suggests that, “We’re not dealing with a consistent product.”


“[The] institutions that have been marketing to the American People have been the CDC, the NIH, the FDA and the Mainstream Media. Those have been the marketers. Those have been the propaganda arms, those have been the ones misleading the American People to line themselves up – and unfortunately, in some cases, to line their children up – to be injected with an unapproved, experimental biological agent.

“Pfizer has not acted as a marketer and if they do, there’s a…whole slew of multi-billion-many-times-over lawsuits that can be brought against them.”

“So there will be criminal charges, plus they have two weeks to come clean as to what is in these injections.
So if these injections are not consistent in all of the ingredients from the microgram – the 30 mcgs of mRNA, to only containing the four lipids, including the one PEGylated lipid with polyethylene glycol – which also was not disclosed, really to the American People. That was only available before the package insert came out and the IND Application, Initial New Drug Application and Phase 3. It was not in the HCP Fact Sheet, originally. I did not see it there. Maybe I misspoke, but I read that thing many times and couldn’t find it there.

“So there was a lot of information that was not disclosed to the American People and that could be interpreted as intentionally misleading them with intention to harm.”
 
Last edited:
  • Like
Reactions: atlkvb

Our STN: BL 125742/0

BLA APPROVAL

BioNTech Manufacturing GmbH
August 23, 2021 Attention: Amit Patel
Pfizer Inc. 235 East 42nd Street New York, NY 10017

Dear Mr. Patel: Please refer to your Biologics License Application (BLA) submitted and received on May 18, 2021, under section 351(a) of the Public Health Service Act (PHS Act) for COVID-19 Vaccine, mRNA.

LICENSING
U.S. Food & Drug Administration 10903 New Hampshire Avenue Silver Spring, MD 20993 w ww.fda.gov We are issuing Department of Health and Human Services U.S. License No. 2229 to BioNTech Manufacturing GmbH, Mainz, Germany, under the provisions of section 351(a) of the PHS Act controlling the manufacture and sale of biological products. The license authorizes you to introduce or deliver for introduction into interstate commerce, those products for which your company has demonstrated compliance with establishment and product standards.

Under this license, you are authorized to manufacture the product, COVID-19 Vaccine, mRNA, which is indicated for active immunization to prevent coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in individuals 16 years of age and older.

The review of this product was associated with the following National Clinical Trial (NCT) numbers: NCT04368728 and NCT04380701.

MANUFACTURING LOCATIONS
Under this license, you are approved to manufacture COVID-19 V
 
 

9cc50f2a7a1299dbd885f9e1d83e5da4.jpg
 
DrZevZelenko
·
2h

In my medical opinion the Pfizer vaccine causes:

Blood clots

Heart inflammation

Miscarriages

Cancers

Autoimmune disease

Potential infertility

Potential ADE


Vladimir Zev Zelenko MD
 
  • Like
Reactions: atlkvb
ADVERTISEMENT
ADVERTISEMENT