Pharmacogenomics (PGx) studies how genetic variations impact your response to drugs. By analyzing your genes, we predict how your body metabolizes medications — helping providers tailor prescriptions to minimize side effects and maximize effectiveness.
How PGx testing works
Sample collection
A simple at-home saliva sample or cheek swab — no needles, no lab visit.
Lab analysis
State-of-the-art laboratory analysis of your genetic data with maximum precision.
Comprehensive report
A detailed PGx report outlining your genetic profile and medication recommendations.
Consultation
We guide you and your provider through your personalized treatment options.
Why choose HFS PGx testing?
Personalized treatment
Medication recommendations based on your genetic profile — the most effective treatment for you specifically.
Minimize side effects
Reduce adverse reactions by using medications that are genetically compatible with your unique makeup.
Cost effective
Avoid the trial-and-error approach to medications and save money on healthcare expenses over time.
Safer management
Avoid medications that are genetically incompatible with your metabolism before problems arise.
Optimized dosing
Determine the ideal dosage for your medications, improving efficacy and reducing risk.
Non-invasive & safe
Safe, non-invasive testing performed by genetic professionals in accredited laboratories.