adoe_ophtha {pharmaverseadam}

Dataset adoe_ophtha

Description

adoe_ophtha dataset

Usage

adoe_ophtha

Format

A data frame with 98 columns:

STUDYID

Study Identifier

DOMAIN

Domain Abbreviation

USUBJID

Unique Subject Identifier

OESEQ

Sequence Number

OECAT

Category for Ophthalmic Test or Exam

OESCAT

Subcategory for Ophthalmic Test or Exam

OEDTC

Date/Time of Collection

VISIT

Visit Name

VISITNUM

Visit Number

VISITDY

Planned Study Day of Visit

OESTRESN

Numeric Result/Finding in Standard Units

OESTRESC

Character Result/Finding in Std Format

OEORRES

Result or Finding in Original Units

OETEST

Name of Ophthalmic Test or Exam

OETESTCD

Short Name of Ophthalmic Test or Exam

OETSTDTL

Ophthalmic Test or Exam Detail

OELAT

Laterality

OELOC

Location Used for the Measurement

OEDY

Study Day of Visit/Collection/Exam

OEMETHOD

Method of Test or Examination

OEORRESU

Original Units

OESTRESU

Standard Units

OESTAT

Completion Status

OETPT

Planned Time Point Name

OETPTNUM

Planned Time Point Number

TRTSDT

Date of First Exposure to Treatment

TRTEDT

Date of Last Exposure to Treatment

TRT01A

Actual Treatment for Period 01

TRT01P

Planned Treatment for Period 01

STUDYEYE

Study Eye Location

AVAL

Analysis Value

AVALC

Analysis Value (C)

AVALU

Analysis Value Unit

DTYPE

Derivation Type

AFEYE

Affected Eye

PARAM

Parameter

PARAMCD

Parameter Code

ADT

Analysis Date

ADY

Analysis Relative Day

ATPTN

Analysis Timepoint (N)

ATPT

Analysis Timepoint

AVISIT

Analysis Visit

AVISITN

Analysis Visit (N)

BASETYPE

Baseline Type

ONTRTFL

On Treatment Record Flag

ABLFL

Baseline Record Flag

ANL01FL

Analysis Flag 01

ANL02FL

Analysis Flag 02

WORS01FL

Worst Post Baseline Obs

BASE

Baseline Value

BASEC

Baseline Value (C)

CHG

Change from Baseline

PCHG

Percent Change from Baseline

ASEQ

Analysis Sequence Number

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

Time of Last Exposure Imput. Flag

TRTDURD

Total Treatment Duration (Days)

SCRFDT

Screen Failure Date

EOSDT

End of Study Date

EOSSTT

End of Study Status

FRVDT

Final Retrievel Visit Date

RANDDT

Date of Randomization

DTHDT

Date of Death

DTHADY

Relative Day of Death

LDDTHELD

Elapsed Days from Last Dose to Death

LSTALVDT

Date Last Known Alive

AGEGR1

Pooled Age Group 1

SAFFL

Safety Population Flag

RACEGR1

Pooled Race 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 admiralophtha package (template ad_adoe.R).

References

None

Examples

data("adoe_ophtha")