Because codes for Patient Safety Indicators often do not map directly from ICD-9 to ICD-10, the transition to ICD-10 may cause the frequency of adverse events to be misreported, according to a recent ...

The Office of the National Coordinator for Health Information Technology, Agency for Healthcare Research and Quality and Food and Drug Administration have announced the winner of the Reporting Patient ...

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 ...

The U.S. Food and Drug Administration is now providing real-time, daily publication updates on adverse event data from its reporting system. In an effort to modernize and provide transparency on ...

In a regulatory filing, the company stated: “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 ...

Randomized, Placebo-Controlled, Phase III Trial of Sunitinib Plus Prednisone Versus Prednisone Alone in Progressive, Metastatic, Castration-Resistant Prostate Cancer A review of citations from PubMed, ...

Minnesota had 38 more medication errors, falls and other adverse health events between October 2022 and October 2023 at hospitals across the state than the previous year. Mayo Clinic saw 10 fewer ...

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 ...

Minnesota had 38 more medication errors, falls and other adverse health events between October 2022 and October 2023 at hospitals across the state than the previous year. Mayo Clinic saw 10 fewer ...