ae: Simulated adverse events for patients receiving two study...

aeR Documentation

Simulated adverse events for patients receiving two study agents.

Description

Simulated adverse events for patients receiving two study agents.

Usage

ae

Format

A data frame with 394 rows and 9 variables:

Subject

Patient ID

ae_detail

Adverse event detail, also known as lowest level term

ae_category

Adverse event category, also known as system organ class

CTCAE5_LLT_NM

Common Terminology Criteria for Adverse Events (CTCAE) version 5

AE_VERBATIM_TRM_TXT

Adverse event verbatim text entered by clinical registered nurse, for "Other, specify"

AE_SEV_GD

Adverse event severity grade, scale from 1 to 5

AE_ONSET_DT_INT

Adverse event onset date

CTC_AE_ATTR_SCALE

Attribution scale of adverse event to first study agent

CTC_AE_ATTR_SCALE_1

Attribution scale of adverse event to second study agent


BiostatsUHNplus documentation built on Sept. 10, 2025, 5:08 p.m.