ReasonShield PGx
Your Genes. Your Medications. Personalized.
Pharmacogenomic interpretation that turns raw genetic data into actionable, guideline-backed medication recommendations — for patients and the clinicians treating them.
What You Get
Guideline-backed pharmacogenomic intelligence for every prescription decision.
Covers CYP2D6, CYP2C19, CYP2C9, DPYD, TPMT, SLCO1B1, HLA-A, HLA-B, and 13 more.
Drug-gene interactions and dosing guidance for 870+ commonly prescribed medications.
Recommendations follow CPIC, DPWG, and FDA pharmacogenomic guidelines.
Reports classify each gene as poor, intermediate, normal, rapid, or ultra-rapid metabolizer.
Accepts clinical VCF files plus 23andMe and Ancestry exports — meet patients where their data lives.
Encrypted storage and processing with provider portal access controls.
A Sample Report, At A Glance
Each gene is classified into a metabolizer phenotype, then mapped to dosing guidance for relevant medications. Clinicians see green for safe, amber for caution, red for avoid or alternative — no PhD in genomics required.
Bring Your Own Genetic Data
No need to redo a test. Upload what you already have.
Clinicians
Provider portal with patient-level reports and dosing guidance at point of care.
Patients
Plain-language insights into how your genes shape medication response.
Personalize Every Prescription
Upload your data or onboard your clinic to ReasonShield PGx today.