df_adverse_events: Simulated Adverse Event Database
In gtreg: Regulatory Tables for Clinical Research
df_adverse_events R Documentation
Simulated Adverse Event Database
Description
A data set containing reported AEs from a trial.
Usage
df_adverse_events
Format
A data frame with 100 rows–one row per patient per AE
- patient_id
Patient ID
- trt
Treatment Group
- system_organ_class
System Organ Class
- adverse_event
Adverse Event
- grade
Grade
- drug_attribution
Drug Attribution
- any_complication
Any Grade Complication
- grade3_complication
Grade 3+ Complication
gtreg documentation built on April 4, 2025, midnight
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| df_adverse_events | R Documentation |
Simulated Adverse Event Database
Description
A data set containing reported AEs from a trial.
Usage
df_adverse_events
Format
A data frame with 100 rows–one row per patient per AE
- patient_id
Patient ID
- trt
Treatment Group
- system_organ_class
System Organ Class
- adverse_event
Adverse Event
- grade
Grade
- drug_attribution
Drug Attribution
- any_complication
Any Grade Complication
- grade3_complication
Grade 3+ Complication
R Package Documentation
Browse R Packages
We want your feedback!
Note that we can't provide technical support on individual packages. You should contact the package authors for that.
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