Aggregate Data Presentation

Present verified outputs without changing their meaning. Do not calculate a clinical conclusion, select an analysis, or repair source discrepancies.

Mandatory table metadata

Every table should identify:

• artifact and analysis purpose;
• data cut and source-output version;
• analysis population/set;
• treatment/group labels;
• denominator for every group and row when it varies;
• whether a value is a subject count, event count, observation count, or estimate;
• units, time point/window, and summary statistic;
• missing, unknown, not assessed, suppressed, or not applicable values;
• coding dictionary/version/language where applicable;
• statistical method and multiplicity status only when copied from a verified output;
• provenance manifest and reviewer status.

Counts and denominators

• Show n/N (%), not a percentage alone, unless the governing output specifies another form.
• Require 0 <= n <= N and N > 0.
• Recalculate only for consistency checking; do not silently replace the reported percentage.
• State the rounding rule and tolerance.
• Do not add subgroup percentages when the subgroup denominator is unknown.
• Do not infer that denominators are randomized, treated, evaluable, or safety populations.
• Keep event counts distinct from subjects affected; event counts can exceed the number of subjects.
• Do not sum non-mutually-exclusive categories.

Dates and time

• Use ISO 8601 in structured manifests.
• Preserve source timezone and precision.
• Distinguish event date, collection date, database cut, report date, and verification date.
• Flag start-after-end and conflicting dates.
• Do not impute a missing day, month, timezone, or chronology.
• For de-identified case reports, use an authorized relative timeline; do not distort intervals.

Units and precision

• Preserve source units.
• Require a unit for every dimensional quantity.
• Use one verified unit per comparable series or expose the mismatch.
• Do not convert or normalize without an authorized traceable conversion rule.
• Preserve clinically meaningful precision; do not create extra significant digits.
• Identify SD, SE, CI, IQR, range, and denominator explicitly.

Missing and suppressed values

Keep these states distinct:

• missing;
• not_collected;
• not_assessed;
• unknown;
• not_applicable;
• suppressed_for_privacy;
• zero.

Never convert a blank to zero. State small-cell suppression rules and ensure totals or complementary cells do not reveal suppressed values.

Adverse-event tables

For term-level aggregate tables:

• state MedDRA version and language;
• state analysis set and denominator;
• state counting rule from the verified SAP/output;
• show subjects affected and event count separately;
• do not add p-values or causal labels;
• do not interpret between-group differences;
• preserve threshold rules exactly;
• have safety and statistical reviewers verify deduplication, hierarchy, and population.

Figures

No figure is mandatory. Create one only when requested, supported by verified aggregate data, allowed by the target guidance, and reviewable without external image generation.

A CONSORT flow diagram is part of CONSORT 2025 reporting, but every count and reason must come from verified trial outputs. A missing count remains missing; do not create a decorative or inferred diagram.

Deterministic consistency check

consistency_checker.py can inspect:

• ISO date and range ordering;
• unit-label consistency;
• n/N (%) arithmetic;
• component-total arithmetic.

It reports mismatches and review needs. It does not change the input, choose the correct source, or validate clinical/statistical meaning.