25+
The 25+ Medications Mehri Tried
Five generations of bipolar disorder. Over 10 years she tried 25+ medications. Pharmacogenomics testing at Mayo Clinic matched her to the right drug within weeks.
For Chronic Patients
3 years on the wrong dose — this can be avoided.
150+ pharmacogenomics rules covering blood pressure, cholesterol, blood thinner, and psychiatric medications. Import your data and get personalized medication guidance in 5 minutes.
150+ PGx rulesLocal analysis5 min resultsClinVar / PharmGKB sourced
The hidden cost of chronic medication
Trial-and-error is not the only path.
~50%
First-try psychiatric drug success rate
Only about half of patients respond to the first psychiatric medication tried. For CYP2D6 poor metabolizers, standard doses may be ineffective or cause severe side effects.
7+
Average number of medications for adults 65+
Polypharmacy interactions are severely underestimated. Warfarin + antibiotics, statin + fibrate — these combinations carry genomic risks that can be predicted.
Solution
Not a prescription. How your genes interact with your medications.
- 1Import existing data: supports WeGene / 23andMe / BGI txt and VCF formats — no re-sequencing needed
- 2150+ pharmacogenomics rules: covering CYP2D6, CYP2C19, CYP3A4, and other key metabolic enzymes
- 3Multi-drug interaction check: automatically scans for genomic conflicts when taking multiple medications
- 4Traceable evidence: every result linked to PharmGKB / CPIC clinical guidelines and PubMed literature
Clopidogrel (antiplatelet)
CYP2C19 — Poor metabolizers show 30-50% reduced efficacy, significantly increasing cardiovascular event risk
Warfarin (anticoagulant)
CYP2C9 / VKORC1 — Genotype determines 3-5x differences in starting dose
Statins (cholesterol)
SLCO1B1 — Specific variants increase myopathy risk 4-17x
SSRI antidepressants
CYP2D6 — Ultrarapid metabolizers may find them ineffective; poor metabolizers face higher side-effect risk
Real stories
Genomics is changing how medications are prescribed
M
Mehri Coulter
Mother of three
"Pharmacogenomics absolutely saved my life — and my kids' lives. Ten years, 25+ medications, horrific side effects including exploding head syndrome. Mayo Clinic's gene test changed my life within weeks."
K
Kristen Davis
Major depression patient
"The gene test showed I metabolize most antidepressants poorly. My doctor selected a gene-matched medication. Without this test, I might still be cycling through endless trial and error."
FAQ
Do I need to get re-tested?
Usually not. If you already have raw data from WeGene, 23andMe, or BGI, you can import it directly. The platform runs pharmacogenomics analysis based on the variant information already present in your file.
Can the results replace my doctor's prescription advice?
No. The platform provides scientific evidence about gene-drug metabolism relationships. Final medication decisions must be made by a physician based on your clinical situation. Use the results as a powerful reference for those conversations.
Which medications are covered by multi-drug interaction checking?
Currently 150+ commonly prescribed medications, including blood pressure, cholesterol, anticoagulant, diabetes, psychiatric, and antibiotic drugs. The rule engine updates continuously with new medications added regularly.
Is my data secure?
All analysis runs locally on your device. Raw files are never uploaded to the cloud. We hold SOC 2 Type II and ISO 27001 information security certifications.
Your genes already know which medications work best for you.
10,000+ users have imported their data and discovered critical medication insights. You could be next.