Biden Administration Pressured The FDA So They Ignored The Risks The NIH and the Biden Administration misled the public and exacerbated the effects of the COVID-19 pandemic through mandates and misinformation. Congressional oversight, including investigative work performed by the Select Subcommittee on the Coronavirus Pandemic, has already revealed how the NIH and the Biden Administration misled the public and exacerbated the effects of the COVID-19 pandemic through mandates and misinformation.40 This interim report reveals that where the Trump Administration organized a total government solution and generated vaccines under EUA, the Biden Administration politicized the administrative state to do things beyond the agencies’ legal authority that, in turn, undermined the federal efforts. The FDA succumbed to the Biden Administration's pressure to act beyond its authority, which may have long-term impacts on the agency's ability to confidently serve the American public. This poor policy by the Biden Administration reveals many significant problems related to accountability and good decision making in the administrative state that warrant legislative reform. Read the full interim staff report and appendix judiciary.house.gov judiciary.house.gov The transcribed interviews and internal FDA documents revealed that, despite evidence of harms from the EUA vaccine, the Biden Administration sought to fully approve the Pfizer vaccine through the Biologics Licensing Application (BLA) process. Under the leadership of then-Acting FDA Commissioner Dr. Janet Woodcock, a long-time FDA staffer who the Biden Administrative promoted to Acting Commissioner, and Dr. Peter Marks, head of the FDA’s Center for Biologics Evaluation and Research (CBER), the agency cut corners in its usually rigorous BLA process to brand the Pfizer EUA vaccine as the only fully licensed “safe and effective” COVID-19 vaccine on the market at the time.23 The BLA approval occurred despite the objections of the FDA’s experts in vaccine development who were concerned about risks for healthy young people caused by the Pfizer vaccine, particularly the risk of myocarditis.24 [That certain people here hand wave away and pretend doesnt exist] The decision for the FDA to rush the Pfizer BLA vaccine review process comported with pressure to mandate the vaccine. Dr. Marks testified to the Subcommittee that he was seeking to appease outsiders who wanted to have an approved vaccine that gave them “more confidence” in a vaccine, even though it was the exact same vaccine already on the market under the EUA.25 Dr. Marks also explained that the Biden Administration could not mandate any COVID-19 vaccine unless the FDA first approved a BLA, and in this case, the Pfizer BLA.26 Standing in the way were indications of EUA vaccine injuries in some patients, [they died] and approving the BLA by the deadline being demanded and in the face of these injuries would require lowering standards.27 To ensure a quicker approval, Acting Commissioner Woodcock and Dr. Marks removed the experts who voiced concerns during the BLA process.28 Acting Commission Woodcock and Dr. Marks proceeded, despite the concerns, and completed the approval to meet the deadline that the Biden White House had set.29 The Subcommittee’s oversight also revealed internal CDC steps taken to undermine efforts by members of Congress to clarify the CDC statements about the vaccine’s efficacy. Clarity by the CDC on the impact of the vaccine could have prevented injury.30 Instead, CDC documents reveal that the CDC engaged in conduct that undermined public confidence by actively censoring speech and disregarding attempts from Americans’ elected representatives in Congress to clarify the CDC’s representations about the vaccines.31 By late 2021, the FDA and Dr. Marks, and not the CDC, became advocates for the Pfizer vaccine—a role for the FDA that was unprecedented before the pandemic and outside the proper function of the FDA as authorized by Congress.32 judiciary.house.gov Which is why we wound up with so many people that died and were injured as a result of their faulty gene therapy they labeled a vax. See Vsafe results.
The truthers are the people trying to stop the antivax madness. It is the most ludicrous circular logic to suggest that a government intent on also doing this are acting in bad faith! The antivax movement has caused untold damage and continues to do so!
This doctor disagrees with you. Doctor: All cause mortality spiked after COVID vaccine rollout. https://rumble.com/v3zrcor-doctor-all-cause-mortality-spiked-after-covid-vaccine-rollout..html
