The shady practices of the Food and Drug Administration (FDA) continue in collusion with the pharmaceutical industry making it all about selling drugs and vaccines at the expense of public health and safety. In the latest such story, FDA was caught removing from its website the document explaining why the agency approved Moderna’s COVID-19 vaccine.
The Epoch Times carried out the investigation into FDA’s explanation of the approval of Moderna vaccine. The paper noted that the FDA approved the Moderna vaccine on Jan. 31 without convening its expert vaccine advisory panel.
The FDA approved Moderna’s vaccine on Jan. 31 without convening its expert vaccine advisory panel, a growing trend for the agency.
And if that violation of standards wasn’t enough, FDA quickly removed the document “The Summary Basis for Regulatory Action” it had posted to explain why the Moderna shot was given full approval after The Epoch Times reached out to them with some questions.
Speculations at once rose among those in the loop over the possible causes of FDA’s removal of the document. One piece of info revealed in the document seems to directly show CDC’s analysis of the incidence of myocarditis (heart inflammation) following vaccination with the Moderna shot in young men.
The FDA meta-analysis examined data of four health care claims databases and estimated that, among males aged 18 to 25, the rate of myocarditis following Moderna’s primary series was 148 per million males vaccinated.
The CDC analysis had “estimated” a maximum of only 56 cases per million males after both Moderna doses. Roman Balmako of The Epoch Times summarized the story in a video report.
Mainstream media outlets, which have long been sold out to the pharmaceutical industry, observed a blanket silence on this story. Some conservative and independent sites reposted the story by The Epoch Times.