Congressman Introduces Bill to Force FDA to Release Pfizer Documents Within 100 Days, Instead of 55 Years

[link to childrenshealthdefense.org (secure)]

According to the complaint:

“The medical and scientific community and the public have a substantial interest in reviewing the data and information underlying the FDA’s approval of the Pfizer Vaccine. Reviewing this information will settle the ongoing public debate regarding the adequacy of the FDA’s review process. Releasing this data should also confirm the FDA’s conclusion that the Pfizer Vaccine is safe and effective and, thus, increase confidence in the Pfizer Vaccine.

“The public’s need for this information is urgent given the fact that COVID-19 vaccines are being mandated to individuals across the country by federal, state and local governments as well as private businesses.”

In a Nov. 19 blog post, Siri wrote that the first 91 pages had been produced. However, some information was redacted, raising questions about what the FDA views as “confidential.”

Siri wrote:

“Pfizer explains, on page 6, that ‘Due to the large numbers of spontaneous adverse event reports received for the product, [Pfizer] has prioritized the processing of serious cases …’ and that Pfizer ‘has also taken a [sic] multiple actions to help alleviate the large increase of adverse event reports’ including ‘increasing the number of data entry and case processing colleagues’ and ‘has onboarded approximately [REDACTED] additional full-time employees (FTEs).’”