1.5M
ER visits per year from adverse drug events
PHARMACOGENOMIC DECISION SUPPORT
Gene results already exist.No one sees them at prescribing.
PGx results, surfaced at order entry for pharmacist and prescriber review.
scroll
THE GAP
The science exists. The workflow does not.
Adverse drug events cause 1.5 million ER visits per year. Over 90% of patients carry at least one actionable pharmacogenetic variant — yet PGx results almost never reach the prescriber at the moment of ordering.
90%+
of patients carry an actionable PGx variant
34
genes with CPIC prescribing guidelines covering 164 drugs
HOW IT WORKS
Not another alert. A decision-ready PGx card.
Existing PGx results fire at the prescribing moment via CDS Hooks. Pharmacists and prescribers see gene results, renal function, and interactions in one patient-specific view.
Recall PGx results on file
Surface gene-drug interactions from existing lab data.
Generate a patient-specific risk card
Gene + renal + interactions + history in one view.
Deliver guidance at order entry
Alternative to review · Dose consideration · Proceed with monitoring.
TRACTION
Designed for real hospital workflows.
Structured around CPIC/FDA pharmacogenomic guidance · Designed for SMART on FHIR + CDS Hooks EHR workflows
Ten Fourteenth · jeremy26@illinois.edu