What is the category of the adverse experience? |
What is the subcategory of the adverse experience? |
What is the adverse experience identifier? |
What is the adverse experience term? |
What is the adverse experience start date? |
Ongoing |
What was the adverse experience end date? |
What is the severity of the adverse experience? |
Was the experience serious? |
Did the adverse experience result in death? |
Was the adverse experience life threatening? |
Did the adverse experience result in initial or prolonged hospitalization for the
subject? |
Did the adverse experience result in disability or permanent damage? |
Was the adverse experience associated with a congenital anomaly or birth defect? |
Was the adverse experience a medically important event not covered by other "serious"
criteria? |
Was this adverse experience related to study product? |
What action was taken with study product? |
What other action was taken? |
What was the action taken with a device? |
What was the outcome of this adverse experience? |
Was this adverse experience related to a device? |
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Mild Moderate Severe |
No Yes |
No Yes |
Yes No |
No Yes |
No Yes |
No Yes |
No Yes |
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