ae | R Documentation |
Simulated adverse events for patients receiving two study agents.
ae
A data frame with 394 rows and 9 variables:
Patient ID
Adverse event detail, also known as lowest level term
Adverse event category, also known as system organ class
Common Terminology Criteria for Adverse Events (CTCAE) version 5
Adverse event verbatim text entered by clinical registered nurse, for "Other, specify"
Adverse event severity grade, scale from 1 to 5
Adverse event onset date
Attribution scale of adverse event to first study agent
Attribution scale of adverse event to second study agent
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