A newly released interim report from Senator Ron Johnson’s office claims top U.S. health officials in the Biden administration withheld critical information in early 2021 about potential heart-related side effects associated with mRNA COVID-19 vaccines. The 54-page report alleges that despite receiving multiple warnings about the risks—particularly cases of myocarditis and related conditions in young people—federal agencies delayed issuing formal alerts for several months.
According to the report, health officials at the Centers for Disease Control and Prevention (CDC) and Food and Drug Administration (FDA) were informed as early as February 2021 about international concerns, including an attempt by Israel’s Ministry of Health to raise alarm over roughly 40 myocarditis cases tied to the Pfizer vaccine. At that time, Israel’s vaccination campaign was further along than the U.S.’s, offering an early view of potential adverse effects.
In response to Israel’s outreach, FDA officials acknowledged limitations in existing data and asked for further information. However, despite growing domestic reports of heart inflammation—more than 158 cases by April—the agencies did not formally update the public until late June. The vaccine was nonetheless approved for adolescents in May.
By late May, internal deliberations began over whether to issue a Health Alert Network (HAN) message, which is typically used by the CDC to quickly notify clinicians and public health departments of emerging health threats. Some officials reportedly feared sounding “alarmist.” Others questioned whether the data truly warranted a full-scale warning. Ultimately, the HAN alert was shelved in favor of a more subdued website notice issued on May 28.
In the interim, internal talking points continued to describe the condition as rare and urged continued vaccination. The official FDA label for both the Pfizer and Moderna vaccines wasn’t updated to reflect the myocarditis risk until June 25.
The report, while critical, notes that many individuals who developed myocarditis, pericarditis, or myopericarditis after vaccination experienced a resolution of symptoms, a finding consistent with CDC data.
Senator Johnson, a frequent critic of the federal pandemic response, has argued that transparency was lacking during this period. “The full extent of the Biden administration’s failure to immediately warn the public about all COVID-19 vaccine adverse events must be completely exposed,” the report concludes.
Health officials involved in the decisions, including then-FDA commissioner Dr. Janet Woodcock and then-CDC director Dr. Rochelle Walensky, have not yet publicly responded to the findings in the interim report.
The release comes amid ongoing political scrutiny over pandemic-era decision-making and the future of public health communications in the wake of COVID-19. The Biden administration and health agencies have consistently maintained that the benefits of mRNA vaccines outweigh the risks, particularly during the height of the pandemic when COVID-19 posed a significant public health threat.
As investigations continue, Johnson’s subcommittee says it plans to further examine the internal communications and decision-making processes of the nation’s top health agencies.
Sebastian Valverde
August 19, 2023 at 2:39 pm
I do not believe the Russian Federation Government Statements.
They need to show up all the prove than their have.