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#' Simulated adverse events for patients receiving two study agents.
#'
#' @format A data frame with 394 rows and 9 variables:
#' \describe{
#' \item{Subject}{Patient ID}
#' \item{ae_detail}{Adverse event detail, also known as lowest level term}
#' \item{ae_category}{Adverse event category, also known as system organ class}
#' \item{CTCAE5_LLT_NM}{Common Terminology Criteria for Adverse Events (CTCAE) version 5}
#' \item{AE_VERBATIM_TRM_TXT}{Adverse event verbatim text entered by clinical registered nurse, for "Other, specify"}
#' \item{AE_SEV_GD}{Adverse event severity grade, scale from 1 to 5}
#' \item{AE_ONSET_DT_INT}{Adverse event onset date}
#' \item{CTC_AE_ATTR_SCALE}{Attribution scale of adverse event to first study agent}
#' \item{CTC_AE_ATTR_SCALE_1}{Attribution scale of adverse event to second study agent}
#' }
"ae"
#' Simulated demography for patients.
#'
#' @format A data frame with 12 rows and 2 variables:
#' \describe{
#' \item{Subject}{Patient ID}
#' \item{GENDER_CODE}{Patient gender}
#' }
"demography"
#' Enrollment data
#'
#' Simulated enrollment for patients.
#'
#' @format A data frame with 12 rows and 3 variables:
#' \describe{
#' \item{Subject}{Patient ID}
#' \item{COHORT}{Study cohort for patient}
#' \item{ENROL_DATE_INT}{Enrollment date of patient to study}
#' }
"enrollment"
#' Simulated ineligibility for patients.
#'
#' @format A data frame with 11 rows and 2 variables:
#' \describe{
#' \item{Subject}{Patient ID}
#' \item{INELIGIBILITY_STATUS}{Recorded ineligibility status of patient to study}
#' }
"ineligibility"
#' Simulated study agent 1 for patients.
#'
#' @format A data frame with 12 rows and 2 variables:
#' \describe{
#' \item{Subject}{Patient ID}
#' \item{TX1_DATE_INT}{Study agent 1 start date of patient on study}
#' }
"drug1_admin"
#' Simulated study agent 2 for patients.
#'
#' @format A data frame with 12 rows and 2 variables:
#' \describe{
#' \item{Subject}{Patient ID}
#' \item{TX2_DATE_INT}{Study agent 2 start date of patient on study}
#' }
"drug2_admin"
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