Tabulation domain specifications in this section are organized by domain.
- SDTM Adverse Events (AE)
- SDTM Comments (CO)
- SDTM Concomitant/Prior Medications (CM)
- SDTM Demographics (DM)
- SDTM Device Identifiers (DI)
- SDTM Device-in-Use (DU)
- SDTM Device Properties (DO)
- SDTM Disposition (DS)
- SDTM ECG Test Results (EG)
- SDTM Exposure (EX)
- SDTM Exposure as Collected (EC)
- SDTM Findings About Events or Interventions (FA)
- SDTM Inclusion/Exclusion Criteria Not Met (IE)
- SDTM Laboratory Test Results (LB)
- SDTM Medical History (MH)
- SDTM Pharmacokinetics Concentrations (PC)
- SDTM Pharmacokinetics Parameters (PP)
- SDTM Product Accountability (DA)
- SDTM Protocol Deviations (DV)
- SDTM Questionnaires (QS)
- SDTM Related Records (RELREC)
- SDTM Respiratory System Findings (RE)
- SDTM Subject Characteristics (SC)
- SDTM Subject Elements (SE)
- SDTM Subject Visits (SV)
- SDTM Substance Use (SU)
- SDTM Supplemental Qualifiers (SUPP--)
- SDTM Tobacco Product Events and Malfunctions (EM)
- SDTM Trial Arms (TA)
- SDTM Trial Elements (TE)
- SDTM Trial Inclusion/Exclusion Criteria (TI)
- SDTM Trial Summary (TS)
- SDTM Trial Visits (TV)
- SDTM Vital Signs (VS)
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