PGxPocket

PGxPocket is a clinician-focused pharmacogenomics (PGx) decision support app that turns a patient’s existing genetic test results into practical prescribing guidance. Users upload a PGx report PDF or connect via FHIR to pull structured genotype/phenotype data, then select a medication to see guideline-based recommendations (e.g., CPIC/DPWG), dosing considerations, and high-risk gene–drug interactions. It generates a short, printable note for the chart and a patient-friendly summary to reduce confusion and nonadherence. This is not a consumer genomics app; it’s built for real workflows in primary care, psychiatry, pain management, and cardiology where medication trial-and-error is common. The MVP focuses on a narrow set of high-impact medications (SSRIs, TCAs, clopidogrel, warfarin, codeine/tramadol) and expands only when evidence and demand justify it.