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Concomitant Medications Analysis

Usage

adcm

Format

A data frame with 95 columns:

STUDYID

Study Identifier

USUBJID

Unique Subject Identifier

SUBJID

Subject Identifier for the Study

SITEID

Study Site Identifier

COUNTRY

Country

DOMAIN

Domain Abbreviation

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

RFPENDTC

Date/Time of End of Participation

SCRFDT

Screen Failure Date

FRVDT

Final Retrieval Visit Date

DTHDTC

Date/Time of Death

DTHADY

Relative Day of Death

DTHFL

Subject Death Flag

LDDTHELD

Elapsed Days from Last Dose to Death

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

DTHDOM

Domain for Date of Death Collection

DTHB30FL

Death Within 30 Days of First Trt Flag

REGION1

Geographic Region 1

DMDTC

Date/Time of Collection

DMDY

Study Day of Collection

AGE

Age

AGEU

Age Units

AGEGR1

Pooled Age Group 1

SEX

Sex

RACE

Race

RACEGR1

Pooled Race Group 1

ETHNIC

Ethnicity

SAFFL

Safety Population Flag

ARM

Description of Planned Arm

ARMCD

Planned Arm Code

ACTARM

Description of Actual Arm

ACTARMCD

Actual Arm Code

TRTP

Planned Treatment

TRTA

Actual Treatment

TRT01P

Planned Treatment for Period 01

TRT01A

Actual Treatment for Period 01

TRTSDT

Date of First Exposure to Treatment

TRTSDTM

Datetime of First Exposure to Treatment

TRTSTMF

Time of First Exposure Imput. Flag

TRTEDT

Date of Last Exposure to Treatment

TRTEDTM

Datetime of Last Exposure to Treatment

TRTETMF

Treatment End Datetime Imput Flag

APHASE

Phase

APHASEN

Description of Phase N

EOSSTT

End of Study Status

EOSDT

End of Study Date

RFICDTC

Date/Time of Informed Consent

RANDDT

Date of Randomization

LSTALVDT

Date Last Known Alive

TRTDURD

Total Treatment Duration (Days)

DTHDT

Date of Death

DTHDTF

Date of Death Imputation Flag

DTHCAUS

Cause of Death

DTHCGR1

Cause of Death Reason 1

CMSEQ

Sequence Number

CMDECOD

Standardized Medication Name

CMTRT

Reported Name of Drug, Med, or Therapy

CMCLAS

Medication Class

CMSTDTC

Start Date/Time of Medication

ASTDT

Analysis Start Date

ASTDTM

Analysis Start Date/Time

ASTDTF

Analysis Start Date Imputation Flag

ASTTMF

Analysis Start Time Imputation Flag

CMENDTC

End Date/Time of Medication

AENDT

Analysis End Date

AENDTM

Analysis End Date/Time

AENDTF

Analysis End Date Imputation Flag

AENTMF

Analysis End Time Imputation Flag

ASTDY

Analysis Start Relative Day

CMSTDY

Study Day of Start of Medication

AENDY

Analysis End Relative Day

CMENDY

Study Day of End of Medication

ADURN

Analysis Duration (N)

ADURU

Analysis Duration Units

ANL01FL

Analysis Flag 01

ONTRTFL

On Treatment Record Flag

PREFL

Pre-treatment Flag

FUPFL

Follow-up Flag

AOCCPFL

1st Occurrence of Preferred Term Flag

CMINDC

Indication

CMDOSE

Dose per Administration

CMDOSU

Dose Units

CMDOSFRQ

Dosing Frequency per Interval

CMROUTE

Route of Administration

CMSPID

Sponsor-Defined Identifier

CMENRTPT

End Relative to Reference Time Point

VISITNUM

Visit Number

VISIT

Visit Name

VISITDY

Planned Study Day of Visit

CMDTC

Date/Time of Collection

Source

Generated from admiral package (template ad_adcm.R).

References

None

Examples

data("adcm")