Safety consent is your explicit agreement to let Unfair use safety signals, logs, and recommendation constraints to reduce risk.
Why it matters
Clear consent is the foundation for consistent guardrails and clearer escalation behavior.
Informed safety checklist
- what data is captured and retention assumptions
- how interaction checks are enabled
- what changes trigger stronger prompts
- how to pause consent and what features are suspended
What to review before enabling high-risk modes
- your medication and supplement overlap
- sleep-sensitive and bleeding-sensitive goals
- willingness to log timing and symptom detail
Withheld consent behavior
If data permission is reduced:
- some adaptation ranking and cross-checks pause
- recommendation depth may be reduced
- safety-first defaults remain active for critical triggers
Practical action step
Review consent options before onboarding and re-confirm any major change in supplement category or goal.
Uncertainty and limits
- Evidence is limited on how strongly consent-aware settings improve outcomes without complete context.
- Evidence is limited on behavior drift after partial consent changes.
Cross-site references
How this appears in Unfair
Safety consent controls what adaptation logic can run and what data depth is available for ranking confidence.
Clinical safety note
If consent is withdrawn, keep current stacks stable and seek clinician review for any required optimization pause.