If an outsider raises questions about contamination of COVID-19 vaccines or how closely the Food and Drug Administration monitors for severe adverse events, the agency considers it a boon to misinformation that lowers vaccine uptake and hence kills people.
If the FDA itself raises these issues, that’s a different story.
The agency turned over nearly 52,000 pages of documents from the “biologic product file of Pfizer’s COVID-19 vaccine for ages 16 and up” earlier this month, in the purportedly final batch required by court order in a Freedom of Information Act lawsuit by the Informed Consent Action Network.
ICAN also put the CDC on the defensive this week with its FOIA production that acknowledged the agency had no scientific research to back its public claim in January that people can safely get their COVID, flu and monkeypox vaccines “at the same time.” The FDA documents, some heavily redacted under the FOIA […]
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