Tag: Clinical safety

According to the World Health Organization, around 1 in 10 patients are harmed in healthcare, with adverse events being a leading cause. This guide explores **what are examples of adverse events** and the critical importance of preventing them in all medical settings.

In clinical research, adverse events (AEs) are any undesirable experiences associated with a medical product or intervention. A standardized grading system, like the widely used Common Terminology Criteria for Adverse Events (CTCAE), is essential for accurately documenting the severity of these reactions and ensuring patient safety.

In medicine, an acronym can have multiple definitions, making context crucial for understanding. What is an AEB diagnosis can refer to several distinct health concepts, most prominently a heart rhythm disturbance or a clinical safety incident.