FDA seeks through the court, to delay for 75+ years the full production of Pfizer’s COVID-19 vaccine clinical trial safety data, which took them only 108 days to review and deem “safe and effective”. [1]
Now the CDC are refusing to produce deidentified adverse event reports (post-marketing safety data) that is actively collected in the CDC’s new v-safe database system, and used by both CDC and FDA to claim the vaccines are safe. [2, 3]
These vaccines are being forced onto the global population, the manufactures are fully exempt of any liability, and now the public health agencies are refusing to prove they are “safe”. The governments are now liable for injury from their “approved” vaccines. If adverse events prove to be far greater than their promoted safety, maybe that is why the transparency they promised in 2020 is no longer their desire?
Lawyer Aaron Siri sums this up as being “dystopian for the government to give pharmaceutical companies billions, mandate Americans to take their products, prohibit Americans from suing for harms, yet refuse to let Americans see the pre- and post-licensure safety data for these products.”
What happens in America, flows onto Australia, as our regulatory authorities work together, not to mention the vaccine manufactures are submitting the same data world wide.