Clinical Decision Support for ADHD Titration

Reach the right dose,
faster.

In-workflow module combining daily patient telemetry with CYP2D6 pharmacokinetic dosing references. Structure the titration journey. Surface the science. Let the clinician decide.

Titration Cockpit
Patient MRD-1001
Atomoxetine 40mg · Day 18 · WATCH
Dose Symptom Side-effect
Appetite suppression — 4 of 5 days
2 missed doses this week
Focus trend improving +1.4 pts
<60s
Daily patient check-in
4
Taps to submit
CYP2D6
PK dosing references
CPIC
Evidence-sourced guidance
How It Works

Structure the titration journey

Titrately bridges the gap between patient visits with structured telemetry and pharmacogenomic reference data.

Structured Between-Visit Capture

Four daily controls — symptom severity, side effects, sleep quality, medication adherence — in under 60 seconds. No dashboard to maintain, no engagement gamification.

Titration Timeline

Dose steps plotted against symptom trend, side-effect flags, and adherence. The prescriber sees a converging picture, not a raw data dump.

Triage-First Queue

Surfaces only patients who need attention — tolerability flags, adherence patterns, pending titration decisions — ranked by clinical urgency.

CYP2D6 PK Dosing References

When a PGx-relevant drug meets a known phenotype, Titrately surfaces the CPIC dosing reference card. Presents the science. Never prescribes.

Embeds in Your Workflow

Surfaces inside the host platform via SMART-on-FHIR/OAuth2. The prescriber never leaves their primary workflow. One integration per host.

Decision Log

Lightweight note + dose change recording. Logs to the outcomes dataset. The prescriber writes the actual Rx in their own EHR.

For Clinicians

Clarity between visits. Science at the point of care.

Standard ADHD titration relies on sparse, retrospective patient self-reports across weeks. Titrately replaces the blind spot with objective, between-visit telemetry alongside validated CYP2D6 reference guidelines.

  • Titration timeline with dose-vs-symptom convergence
  • Tolerability flags surfaced by clinical urgency
  • PK dosing reference cards with CPIC evidence sourcing
  • Triage queue across your entire panel
  • Sovereign clinical decision-making preserved
PK
CYP2D6 Poor Metabolizer
Atomoxetine · PK dosing reference

Reduced CYP2D6 activity leads to higher atomoxetine plasma exposure and slower clearance.

CPIC guidance: consider lower starting dose / slower titration and an extended interval before increasing; recheck tolerability before each step.
PK dosing reference only. Not a treatment recommendation. Clinical decision rests with the prescriber.
For Patients

Your daily titration partner.

Track your journey in under 30 seconds. Share exact symptoms with your doctor so they can support you with confidence. No streaks, no pressure. Missing a day is fine.

  • Four simple controls — one screen, under 60 seconds
  • Neurodiverse-safe interface with calm, low-excitation design
  • Non-punitive gaps — missing a day shows as a gap, not a failure
  • Check-ins stop automatically when your dose stabilizes
  • Your data goes directly to your prescriber
Quick check-in
How was today?
Focus today
😣 😕 😐 🙂 😁
Side effects
None Appetite Sleep Jittery
Took your meds?
On time Late Missed
The Regulatory Line

CDS, not SaMD. References, not recommendations.

Titrately stays on the non-device clinical decision support side of the FDA line by design.

01

Never Prescribe, Always Present

No output contains "Reduce dose to X" or "Change to Y." Only: dosing literature references for this phenotype.

02

Human-in-the-Loop

Every observation is framed as "telemetry ready for review" or "reference material for clinical judgment."

03

Attribute Sources

Every PK reference card links to the published CPIC guideline or PharmGKB annotation. The clinician can independently verify.

04

Boundary on Every Response

"PK dosing reference only. Not a treatment recommendation. Clinical decision rests with the prescriber." On every card, every time.

Structure the titration journey.

Titrately integrates directly into the clinical workflow, organizing frictionless daily symptom signals alongside established pharmacokinetic references.

Open Platform