Settings
Definitions, rules and governance.
Every internal page calculates from one shared analytics layer. Current selection: Last 30 days. 6,265 valid records available in total.
Metric definitions
One calculation per metric, used everywhere.
Total tracked sessionsCount of valid session records in the selected window.Duplicate session IDs and malformed timestamps are excluded.
Unique tracked patientsCount of distinct anonymous patient references.Sessions are never counted as patients. References are never displayed.
Average reported effectivenessMean of patient-reported effectiveness ratings, on a 1–5 scale.Sessions with no rating are excluded. This is reported experience, not efficacy.
Side-effect rateShare of sessions recording at least one side effect.'None' is not counted as a side effect. Denominator is all valid sessions.
Typical durationMost frequently recorded duration band.Sessions with no recorded duration are excluded.
Continued tracking rateShare of patients who recorded another session within 30 days of their first recorded experience.Measures tracking behaviour only. It does not confirm medicine adherence or continued treatment.
Negative experience rateShare of sessions showing at least one observable negative indicator: effectiveness of 1–2, any side effect, duration rated too short or too long, or feeling-after below feeling-before.Each indicator is also reported separately. No hidden composite score is used.
Minimum sample rules
Below these thresholds, comparisons show Not enough data.
Product comparison10 sessions
Batch comparison10 sessions
Cultivar comparison10 sessions
Amount group10 sessions
Pattern callout / insight20 sessions
Trend period10 sessions
Data quality handling
Invalid observations are excluded, never repaired.
- Records without an identity, product reference or parseable timestamp are excluded.
- Duplicate session IDs are counted once.
- Missing effectiveness ratings are excluded from effectiveness averages only.
- Missing duration is excluded from duration and satisfaction views only.
- Missing or non-gram amounts are excluded from amount and dose/outcome views.
- “None” is recorded but never counted as a side effect.
- Batches without a reference record fall back to the product recorded on the session.
- Free-text notes are never read into aggregate reporting.
Coming soon
Access and governance
Team access, taxonomy management and retention policy for the internal platform.
- —Team access and roles
- —Product, cultivar and batch reference management
- —Effect and side-effect taxonomies
- —Data retention and governance
Part of the Ament intelligence platform.
This platform is an internal product, research and patient-experience intelligence layer. It is not intended to support clinical decisions.