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The Food and Drug Administration on Friday started to publicly report adverse events to drugs and some vaccines in real time, a change FDA Commissioner Dr. Marty Makary said promotes “radical transparency.”
The FDA Adverse Event Reporting System, known as FAERS, is what the FDA uses as its primary database for collecting adverse event reports related to medication errors, prescription drugs, and some vaccines — though the main database for vaccine adverse event reports is known as VAERS. The reports are collected from health care professionals, manufacturers, and consumers.
The FAERS public dashboard is available to access online.
“Adverse event reporting should be fast, seamless and transparent,” Makary said in a statement. “People who navigate the government’s clunky adverse event reporting websites should not have to wait months for that information to become public. We’re closing that waiting period and will continue to streamline the process from start to finish.”
Starting today, the FDA will disclose adverse events publicly in real time. #radicaltransparency https://t.co/WLN38ivs1m
— Dr. Marty Makary (@DrMakaryFDA) August 22, 2025
In a press release, the FDA, which is a branch of Health and Human Services (HHS), said the change “represents a significant step forward in modernizing the agency’s safety monitoring infrastructure and demonstrates our commitment to real-time protection of public health.”
“The shift is one of many steps in the FDA’s broader data modernization strategy to streamline all of its adverse event reporting systems and increase reporting frequency across all systems to identify safety signals faster,” the press release added.
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Robert F. Kennedy Jr., who leads HHS, has made a number of changes concerning therapeutics and vaccinations. Most notably, the secretary gutted the Advisory Committee for Immunization Practices, known as ACIP, back in June. The highly influential vaccine panel, Kennedy argued, was plagued with conflicts of interest before he took action.
New members on ACIP include Dr. Robert Malone, who worked on early research for mRNA vaccine technology and is a vocal critic of the mRNA COVID vaccines, as well as other medical experts who took dissenting positions from the medical establishment during the COVID pandemic.
On Monday, I took a major step towards restoring public trust in vaccines by reconstituting the Advisory Committee for Immunization Practices (ACIP). I retired the 17 current members of the committee. I’m now repopulating ACIP with the eight new members who will attend ACIP’s…
— Secretary Kennedy (@SecKennedy) June 11, 2025
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