RSM US LLP ("RSM") – the leading provider of assurance, tax and consulting services for the middle market – has implemented ...

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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 ...

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 ...

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 ...

Vaccine safety monitoring in the US is a multilayered process that combines passive and active functions, as well as expert analyses of specific safety questions. Side effects are passively reported ...

Fred Hutchinson Cancer Center-led investigators found that higher patient-reported fatigue before cancer treatment aligned ...

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 ...