Adverse incident report 2025

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An adverse incident is an event or circumstance that might give rise to a claim, complaint or allegation against you. With claims-made protection, you are required to report an adverse incident to Medical Protection as soon as reasonably practicable after it occurs (or when you become aware that it has occurred).
The Four Types of Incident Reports Incident reports can be categorized into four main types: injury, illness, near miss, and property damage. Each type serves a specific purpose and provides valuable insights into different aspects of workplace safety.
Incident reporting in healthcare refers to collecting healthcare incident data with the goal to improve patient safety and care quality. Done well, it identifies safety hazards and guides the development of interventions to mitigate risks, thereby reducing harm.
An adverse event is a broader term defined by the WHO as a medical occurrence temporally associated with the use of a medicinal product, but not necessarily causally related. Regulatory agencies such as the Food and Drug Administration (FDA) define an adverse event (also referred to as an adverse experience) as any
[Narrator] Examples of adverse information that must be reported include your co-worker exhibiting paranoid behavior, your boss experiencing significant financial problems, or someone attempting to gain access to information outside of their need-to-know.
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The death of a patient. Brain or spinal damage to a patient. The performance of a surgical procedure on the wrong patient. A procedure to remove unplanned foreign objects remaining from a surgical procedure.

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