PGx test
One-time payment · No subscriptions
- Analysis of 50+ common medications
- Categories: psychiatry, cardiology, pain
- Downloadable digital PDF report
- Sample kit with shipping included
- Orientation consult (30 min)
- Valid for life

🧬 Precision medicine · Scientifically backed
Discover how your body metabolizes the medications that matter most. Avoid adverse effects, adjust dosing, and support medical decisions with your DNA.
What is pharmacogenetics?
Your DNA determines how your body processes medications. This test identifies variants in your genes to optimize drug efficacy and minimize risk.
Variants in enzymes such as CYP2D6, CYP2C19, or CYP2C9 affect how quickly your body processes hundreds of common medications.
Based on your genetic profile, your physician can choose the most effective medication and adjust dosing so you get maximum benefit without unnecessary risk.
Your genome does not change. The pharmacogenetic report you receive today is a health tool you can share with any doctor at any time in the future.
What does your pharmacogenetic test analyze?
The PGx pharmacogenetic test analyzes 425 markers covering more than 150 drugs (and combinations) across 15 medical specialties, including these clinical categories.
Who is the pharmacogenetic PGx test for?
Book a free 15-minute call with a clinical genomics specialist.
Book a free consultationNGx report · Sample preview
Your report identifies your metabolic phenotype by category and shows which medications are safe, which need dose adjustments, and which you should avoid.
Choose your pharmacogenetic test
Both plans include the home sampling kit and the full digital report.
One-time payment · No subscriptions
One-time payment · Broader clinical scope
You do not need to go to a lab. The whole process uses a buccal swab sent to your home.
Purchase online and receive your kit in 24–48 hrs with a prepaid return envelope included nationwide in Mexico.
Painless 2-minute cheek swab. Seal the kit and ship it to the lab using the included prepaid label.
In 10–14 days, access your full report by email and book your interpretation consultation with a specialist.
of adverse drug reactions are preventable with appropriate pharmacogenetic information.
million scientific publications support the clinical use of pharmacogenetics in precision medicine.
FDA-approved drugs include pharmacogenetic information on their official labeling.
of people have at least one relevant genetic variant that affects response to common medications.
🔬 NGx Pharmacogenetic Test — Validated by clinical pharmacogenomics. Targeted Genotyping — Agena/Sequenom MassARRAY (iPLEX Gold assay + mass spectrometry) with coverage of CPIC and PharmGKB class A and B variants.
I had spent three years without finding the right antidepressant. The pharmacogenetic test showed I am a slow CYP2D6 metabolizer. With that information my psychiatrist adjusted my medication and I finally responded to treatment.
As a cardiologist, I now order the test for my patients before prescribing clopidogrel or warfarin. The NGx report is clear, CPIC-based, and it completely changes how I make therapeutic decisions.
I had a terrible reaction to codeine prescribed after surgery. Later I learned I am an ultra-rapid metabolizer. I wish I had had this test sooner. Now I share it with every doctor I see.
The NGx pharmacogenomics team is available to answer your questions and help you choose the plan that best fits your clinical situation.
Understand how your DNA influences your medication response and why it matters before your next treatment.
Read articleDiscover how a pharmacogenetic test helps you choose the right medication and avoid side effects.
Read articleWhat a pharmacogenetic test analyzes and how to use the report with your doctor for safer decisions.
Read article