What is adverse event reporting?
Adverse event reporting is the process of documenting and analyzing negative effects or incidents related to medical treatments or interventions.
Why is it important?
It's crucial for patient safety, helps identify potential risks, and improves the overall quality of healthcare.
Who is responsible for reporting these events?
Healthcare professionals, manufacturers, and sometimes patients themselves are responsible for reporting adverse events.
How are these reports used?
Reports are analyzed to identify trends, improve safety protocols, and inform regulatory actions.
Can you give me an example of an adverse event?
Sure! An example would be a patient experiencing severe allergic reactions after receiving a medication.
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