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 ...

The evaluation of drug safety in clinical trials is a critical element of the drug development process, ensuring that therapeutic benefits outweigh potential harms. Clinical trials, particularly in ...

A recent study published in the Journal of Attention Disorders provides new evidence that difficult childhood experiences may ...

The authors examined the association of diabetes with self-reported gaps in care coordination and self-reported preventable adverse events using data from a national sample of older adults. Objectives ...

In a study of outpatient sites, researchers found that 7% of patients experienced at least one adverse event and 1.9% of patients experienced at least one preventable adverse event. The most common ...

Patient safety events, which are adverse events that could have been prevented, are altogether common in outpatient settings and speak to the need for improving safety in these settings, according to ...

For decades, an unassuming government vaccine safety surveillance system has done its job, quickly flagging possible side effects and allowing scientists and regulators to investigate further. But for ...

Objective To identify the optimal dose and type of physical activity to improve functional capacity and reduce adverse events in acutely hospitalised older adults. Design Systematic review and ...

Please provide your email address to receive an email when new articles are posted on . The FDA Adverse Event Reporting System will now host daily publications, instead of quarterly. The agency’s goal ...