Dentists and hygienists are encouraged to report adverse drug and device reactions in the oral cavity of in their patients to improve the U.S. surveillance system and help protect patients' safety, ...
Twenty-three percent of patient deaths attributed to medical devices were classified as something other than patient deaths in the FDA’s adverse events database, a study published July 26 in JAMA ...
When the HSRO approves human-subjects research, the approval is based upon the information about how the research will be conducted and the risks and anticipated benefits to subjects that are known at ...
A recent study sheds light on issues surrounding the system's functionality, transparency, and responsiveness. The Vaccine Adverse Event Reporting System (VAERS), comanaged by the CDC and FDA, may not ...
Robert Moffit, Ph.D., is a senior research fellow in the Center for Health and Welfare Policy at The Heritage Foundation. This is the final piece in an eight-article series on “Restoring Trust in ...
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 ...
NEW YORK & LONDON--(BUSINESS WIRE)--Regulatory Datacorp (RDC) and the FinTech FinCrime Exchange (FFE) revealed the findings of a new report detailing the customer screening practices of FFE members in ...
ROCHESTER — Minnesota hospitals recorded 21 patient deaths and 178 serious injuries last year due to adverse health events, according to the Minnesota Department of Health. From Oct. 7, 2021 to Oct. 6 ...
ST PAUL, Minn. — A new report from the Minnesota Department of Health (MDH) says the number of adverse events and instances of patient harm jumped in 2021, a reflection of the challenges and increased ...
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