The Vaccine Adverse Event Reporting System (VAERS) was established to protect public health. Now it's being used against it.

Vaccine safety monitoring in the US is a multilayered process that combines passive and active functions, as well as expert ...

Shares of LENZ Therapeutics (LENZ) fell ~26% on Friday, a move TD Cowen attributed to investor worries over an adverse event reported on a federal database about the company’s newly launched eye ...

MANKATO — The number of adverse health events, considered “often preventable,” rose overall at south-central Minnesota health care providers during the latest reporting year. The Minnesota Department ...

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The National Quality Forum is aiming to modernize and standardize serious adverse event reporting via a new patient safety effort. Through the “Focus on HARM” initiative, NQF will update the criteria ...

To increase transparency, the agency is publishing data from the FDA Adverse Event Reporting System daily rather than quarterly. (HealthDay News) — The U.S. Food and Drug Administration is now ...

LENZ Therapeutics (LENZ) is aware of a recent adverse event report submitted to the U.S. Food and Drug Administration’s Adverse Event Reporting System database describing a retinal tear in a patient ...

Harm and the potential for harm from medical care is pervasive and well-documented. Much of the safety literature has historically focused on physical harm, but the Agency for Healthcare Research and ...

The FDA announced that adverse event data from the FAERS will now be published daily. HealthDay News — The US Food and Drug Administration is now providing real-time, daily publication updates on ...