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As Department of Health and Human Services (HHS) and FDA leadership continue to look for ways to boost transparency and ...
The FDA said it has begun publishing reports of adverse events concerning drugs on a daily basis, instead of quarterly, as it ...
The FDA has started reporting real-time data about adverse events through the FDA Adverse Event Reporting System, improving ...
The FDA now provides daily updates on adverse event reports for drugs and biologics via FAERS. Read more here.
The U.S. Food and Drug Administration has released more than 20 years of reports detailing adverse events involving medical devices, ending a program that allowed some manufacturers to keep safety ...
The issuance of an adverse event letter by a health care facility is highly significant. They are only issued where there is an injury to the patient, which the medical facility recognizes is due ...
Adverse reactions can still be reported, and data from v-safe is still available to the public, according to a spokesperson for the organization. CDC didn't remove VAERS from website ...
For decades, the Vaccine Adverse Event Reporting System, or VAERS, has been exploited by people opposed to vaccination. Here, we’ll explain how VAERS works and run through five misconceptions ...
An 11-hospital sample of about 2,800 admissions found 978 adverse events, about a third of which were judged to be serious or worse.
Almost one quarter of hospital patients in the U.S. experience an adverse event such as medication-related harm, a pressure injury or infection during their care, according to a new study.
The FDA announced it has commenced daily publication of adverse event data from the FDA Adverse Event Reporting System (FAERS ...
The U.S. Food and Drug Administration has started "real-time reporting of adverse event data," according to an annoucement ...
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