adcm: adcm

adcmR Documentation

adcm

Description

Concomitant Medications Analysis

Usage

adcm

Format

A data frame with 95 columns:

STUDYID

Study Identifier

DOMAIN

Domain Abbreviation

USUBJID

Unique Subject Identifier

CMSEQ

Sequence Number

CMSPID

Sponsor-Defined Identifier

CMTRT

Reported Name of Drug, Med, or Therapy

CMDECOD

Standardized Medication Name

CMINDC

Indication

CMCLAS

Medication Class

CMDOSE

Dose per Administration

CMDOSU

Dose Units

CMDOSFRQ

Dosing Frequency per Interval

CMROUTE

Route of Administration

VISITNUM

Visit Number

VISIT

Visit Name

VISITDY

Planned Study Day of Visit

CMDTC

Date/Time of Collection

CMSTDTC

Start Date/Time of Medication

CMENDTC

End Date/Time of Medication

CMSTDY

Study Day of Start of Medication

CMENDY

Study Day of End of Medication

CMENRTPT

undocumented field

TRTSDT

Date of First Exposure to Treatment

TRTEDT

Date of Last Exposure to Treatment

DTHDT

Date of Death

EOSDT

End of Study Date

TRT01P

Planned Treatment for Period 01

TRT01A

Actual Treatment for Period 01

ASTDTM

Analysis Start Date/Time

ASTDTF

Analysis Start Date Imputation Flag

ASTTMF

Analysis Start Time Imputation Flag

AENDTM

Analysis End Date/Time

AENDTF

Analysis End Date Imputation Flag

AENTMF

Analysis End Time Imputation Flag

ASTDT

Analysis Start Date

AENDT

Analysis End Date

ASTDY

Analysis Start Relative Day

AENDY

Analysis End Relative Day

ADURN

Analysis Duration (N)

ADURU

Analysis Duration Units

ONTRTFL

On Treatment Record Flag

PREFL

Pre-treatment Flag

FUPFL

Follow-up Flag

ANL01FL

Analysis Flag 01

AOCCPFL

1st Occurrence of Preferred Term Flag

APHASE

Phase

APHASEN

Description of Phase N

TRTP

Planned Treatment

TRTA

Actual Treatment

SUBJID

Subject Identifier for the Study

RFSTDTC

Subject Reference Start Date/Time

RFENDTC

Subject Reference End Date/Time

RFXSTDTC

Date/Time of First Study Treatment

RFXENDTC

Date/Time of Last Study Treatment

RFICDTC

Date/Time of Informed Consent

RFPENDTC

Date/Time of End of Participation

DTHDTC

Date/Time of Death

DTHFL

Subject Death Flag

SITEID

Study Site Identifier

AGE

Age

AGEU

Age Units

SEX

Sex

RACE

Race

ETHNIC

Ethnicity

ARMCD

Planned Arm Code

ARM

Description of Planned Arm

ACTARMCD

Actual Arm Code

ACTARM

Description of Actual Arm

COUNTRY

Country

DMDTC

Date/Time of Collection

DMDY

Study Day of Collection

TRTSDTM

Datetime of First Exposure to Treatment

TRTSTMF

Time of First Exposure Imput. Flag

TRTEDTM

Datetime of Last Exposure to Treatment

TRTETMF

Treatment End Datetime Imput Flag

TRTDURD

Total Treatment Duration (Days)

SCRFDT

Screen Failure Date

EOSSTT

End of Study Status

FRVDT

Final Retrievel Visit Date

RANDDT

Date of Randomization

DTHDTF

undocumented field

DTHADY

Relative Day of Death

LDDTHELD

Elapsed Days from Last Dose to Death

DTHCAUS

undocumented field

DTHDOM

undocumented field

DTHCGR1

undocumented field

LSTALVDT

Date Last Known Alive

SAFFL

Safety Population Flag

RACEGR1

Pooled Race Group 1

AGEGR1

Pooled Age Group 1

REGION1

Geographic Region 1

LDDTHGR1

Last Dose to Death - Days Elapsed Grp 1

DTH30FL

Death Within 30 Days of Last Trt Flag

DTHA30FL

Death After 30 Days from Last Trt Flag

DTHB30FL

Death Within 30 Days of First Trt Flag

Source

Generated from admiral package (template ad_adcm.R).

References

None

Examples

data("adcm")

pharmaverseadam documentation built on Oct. 30, 2024, 9:26 a.m.