ADR Intelligent Reporting System

A medication-safety platform that turns clinical instant messages and hospital-data triggers into reviewable ADR signals, report drafts, and traceable submission workflows.

Clinical problem

ADR evidence is often scattered across messages, laboratory abnormalities, medication orders, and patient narratives. Manual reporting is slow and easy to miss during routine clinical work.

Under-reporting Fragmented evidence Manual workload

What I built

A workflow for message monitoring, signal mining, patient self-report intake, report management, CHPS status synchronization, and rule-center configuration.

Signal queue Draft report CHPS sync

My role

I designed the clinical workflow, data logic, review states, and hybrid NLP pipeline that keeps AI assistance subordinate to pharmacist confirmation.

Clinical design Hybrid NLP Human review

Interface Preview

A de-identified English preview generated from the system’s actual front-end structure.

Medication safety

Message-to-ADR review desk

The interface brings together message monitoring, rule-triggered safety signals, LLM-assisted extraction, and pharmacist review before report submission.

  • Clinical IM content and structured triggers are converted into a pharmacist-readable candidate queue.
  • Suspected drug, reaction, timing, evidence, and report completeness can be drafted automatically.
  • Local review state and submitted-report status remain traceable after CHPS synchronization.
ADR Intelligent Reporting System
English interface preview of the ADR intelligent reporting system

AI and data workflow

The value of the system is not only extraction accuracy; it is the translation of noisy clinical traces into a governed pharmacist workflow.

Data inputs

Clinical messages, medication orders, laboratory abnormalities, rescue-medication triggers, patient self-reports, and reporting-system status are normalized into the same review surface.

Messages Orders Labs Reports

Hybrid NLP layer

Rules protect high-value safety signals, while LLM-assisted extraction completes narrative fields and structures candidate ADR evidence for human review.

Rules LLM extraction Confidence

Pharmacist checkpoint

The system supports triage and drafting, but causality assessment, completeness judgment, and final submission remain pharmacist-led.

Review Causality Submission

What this demonstrates

This platform shows implementation ability across clinical pharmacy, AI methods, and real hospital reporting constraints.

Research translation

The work is connected to a 2026 SSRN preprint on zero-friction ADR reporting from clinical instant messaging using hybrid NLP.

SSRN preprint Hybrid NLP Pharmacovigilance

Hospital integration

The system is designed around practical interfaces and review queues rather than isolated model outputs, making it closer to deployable clinical infrastructure.

Workflow Traceability Operations

Safety-first AI

Conservative retention rules preserve high-value signals such as rescue medication and hematologic toxicity flags, reducing the risk of silent misses.

Signal retention Medication safety Human oversight