Top US Vaccine Official Claims Covid Vaccines Caused Child Deaths, Plans Regulatory Changes
TL/DR –
Vinay Prasad, America’s top vaccines official, made claims in a memo that at least 10 children died from Covid vaccination but did not provide evidence or details on the cases. Prasad’s statements, along with his plans to revamp vaccine regulation, have raised concerns among experts who fear the public’s trust in vaccines will be damaged and the number of preventable illnesses will rise. The memo diverges significantly from the regulatory agency’s history and it is considered highly unusual for such information to be shared without convening an advisory committee or publishing data in a public presentation or study.
U.S. Vaccine Official Announces Regulatory Changes Amidst Controversial Claims
America’s leading vaccine official recently pledged to overhaul vaccine regulation, based on an assertion that a minimum of 10 children died from Covid vaccination. However, he furnished no evidence to support this claim nor did he detail the proposed amendments.
Experts express concern that these unilateral decisions, made without consultation or data publication, could jeopardize public trust and lead to the withdrawal of vaccines such as the flu shot. They fear this will result in a hike in vaccine-preventable illnesses.
The reported child deaths were within an age group of seven to 16 from 2021 to 2024, recorded in the Vaccine Adverse Event Reporting System (VAERS), a crowdsourced database, as stated by Vinay Prasad, Chief Medical and Scientific Officer at the US FDA. However, Prasad failed to provide further details of the cases.
In a memo, Prasad expressed that Covid vaccines have caused child fatalities in America, challenging the efficacy of these vaccines. Infectious diseases physician Paul Offit criticized Prasad for making such sensational claims without substantiating them.
Covid vaccines have been administered to millions globally and are recognized as safe and effective. These new claims and the proposed approach deviate greatly from the regulatory agency’s track record.
It’s uncommon for top vaccine regulatory information to be disseminated via email to all staff without convening the Vaccines and Related Biological Products Advisory Committee (VRBPAC) or publicly publishing the data.
Prasad’s memo emphasized myocarditis (heart inflammation) as a potential cause of the child deaths but failed to establish a causative link between the vaccination and the condition. Autopsies, which are standard for unexpected child fatalities, would reveal any such damage.
Prasad’s memo also seemed to echo the concerns of anti-vaccine activists, hinting at the possible detrimental effects of multiple vaccinations, yet offering no substantial evidence.
As a consequence of these assertions, the FDA plans to modify its vaccine regulations, demanding randomized trials demonstrating clinical outcomes rather than just immune responses for most new products.
This new framework presents obstacles for all respiratory vaccines, especially updated flu and Covid vaccines, which are time-sensitive. The removal of these shots in the U.S. could cause more preventable deaths.
Offit expressed that undermining vaccine confidence is highly dangerous and irresponsible, especially considering that children are still being hospitalized and dying from the virus.
The resulting confusion complicates public understanding and trust in health agencies, making it harder for them to discern which recommendations to follow.
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