Here’s what happened:
On March 3, the US Food and Drug Administration (FDA) lost a lawsuit, and the court required the FDA to complete the publication of the 1,32-page full review of the Pfizer new crown vaccine by this summer, and now the FDA has released the first batch of documents.
However, no form of interpretation or organization of the document was provided. A total of 150 documents are currently available for download on its website. However, when it comes to the process of this case, it has been a twist and turn.
Among the many documents, the most shocking is the report on the adverse reactions of the Pfizer vaccine, which is as many as 9 pages, and many netizens exploded in an instant!
More than 1000, adverse reactions are listed in the documents disclosed so far, many of which are seen for the first time, including:
THE DISEASES GIVEN BY PFIZER VACCINE:
Fasciitis, eye swelling, facial paralysis, alopecia areata, anaphylactic shock, pregnancy anaphylaxis syndrome, acute cardiomyopathy, acute respiratory failure, vasculitis at the injection site, epilepsy, thrombosis, arrhythmia, arthritis, asthma, bronchospasm, cardiac arrest, heart failure, chest discomfort, asphyxia, acute lupus erythematosus, acute encephalomyelitis, acute kidney injury, acute macular outer retinopathy, aplastic anemia, chronic autoimmune glomerulonephritis, chronic cutaneous lupus erythematosus, chronic spontaneous urticaria, Hemolytic anemia, colitis, dermatitis, diabetes, embolic cerebral infarction, endocrine disorders, neonatal myasthenia gravis, myelitis, non-infectious oophoritis, thyroiditis, ulcerative proctitis, ocular pruritus, genital herpes, glossopharyngeal nerve palsy, hemorrhagic vasculitis, cervicitis, lupus cystitis, lupus encephalitis, multiple sclerosis, etc.
Taking the FDA to court was the Transparency Public Health and Medical Professionals Organization (PHMPT), a nonprofit organization that first filed a lawsuit against the U.S. Food and Drug Administration (FDA) in the U.S. District Court for the Northern District of Texas last September. Questioned the FDA’s decision to withhold data related to Pfizer and BioNTech’s 9 coronavirus vaccine.
In November last year, the PHMPT organization asked the FDA to fully disclose the vaccine review data, but the FDA did not respond.
Subsequently, the PHMPT organization took the FDA to court. But the F.D.A. applied to a federal judge to disclose only 500 pages of relevant documents each month. In other words, it will take 32 years to disclose all 9,55 pages of information, by 2076!
PHMPT was outraged: by 2076, many of the people who manufactured, approved, and vaccinated would have left this world long ago.
The plaintiffs argued that the FDA violated U.S. federal law that “once a license is granted, data and information from the use of biological products during the licensing process can be publicly disclosed immediately,” contrary to the FDA’s commitment to “complete transparency” before and after the approval of the new crown vaccine.
Details connection: http://phmpt.org/wp-content/uploads/2021/11/5.3.6-postmarketing-experience.pdf
