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What is pharmacogenomic (PGx) testing?

Pharmacogenomics is the study of how your genes affect your response to medications. A PGx test reads a small set of genes from a cheek swab and gives your prescriber information to help choose drugs and doses.

See a sample report
SampleCheek swab
How oftenOnce in a lifetime
Medications77 on the report
Results after lab receipt5–7 days
The basics

Why the same pill works differently for different people

Most medications are processed by enzymes in your liver. The genes that build those enzymes come in different versions. Some versions work faster, some slower, and some barely at all.

That's why one person does well on a standard dose while another gets side effects or no relief. PGx testing finds those differences before a prescription is written, instead of after weeks of trial and error.

Almost half of spontaneously reported adverse drug reactions may have identifiable causes, most likely explained by genetic variability.591–99% of patients in large U.S. programs carried at least one actionable variant.2,3

Too much drug

Slow processing can let a drug build up and cause side effects.

Too little effect

Fast processing can clear a drug before it has time to work.

Prodrugs that never switch on

Some drugs need an enzyme to become active. Without it, they don't work.

The right fit

With PGx results, the prescriber can pick a drug and dose that fits.

Metabolizer types

Where do you fall on the spectrum?

Each gene result places you in a category. Tap one to see what it means, using the CYP2C19 gene as an example.

Slower processingFaster processing

Simplified for education. Prescribing decisions use the full report and the patient's clinical picture.

Key genes

The genes behind most drug-gene interactions

Most drug-gene interactions run through the CYP450 enzymes in the liver. Genes like CYP2D6 have more than 100 known variant alleles.

CYP2D6

Antidepressants, antipsychotics, codeine, tramadol, metoprolol, tamoxifen

CYP2C19

Clopidogrel, SSRIs like citalopram and sertraline, proton pump inhibitors

CYP2C9

Warfarin, NSAIDs like celecoxib and meloxicam, phenytoin

VKORC1

Warfarin sensitivity, used with CYP2C9 to guide dosing

SLCO1B1

Statins, especially simvastatin, and the risk of muscle pain

CYP2B6

Efavirenz and some other medications

TPMT

Thiopurines used in autoimmune disease and some cancers

See them all

Search every medication on the AchieveDx PGx report.

Medication list
Who should consider it

Is PGx testing right for you?

Ask your provider or pharmacist if any of these sound familiar.

Side effects

Medications have caused nausea, fatigue, headaches, dizziness or other unwanted reactions.

Starting something new

Especially for mental health, pain, heart health or long-term therapy.

It isn't working

Your current medication isn't giving the relief or results you expected.

Several prescriptions

More medications means more chances for a drug-gene interaction.

The process

What happens after the swab

  1. Step 1

    Swab

    A quick cheek swab. No needles or blood draw.

  2. Step 2

    Coverage check

    Insurance is verified. Any cost is confirmed with you first.

  3. Step 3

    Lab analysis

    A CLIA-certified lab reads your genes in 5–7 days after it receives the sample.

  4. Step 4

    Review together

    Your provider or pharmacist explains the results and any changes.

Coverage for eligible patients

Medicare covers PGx testing when a clinician is considering or using a specific drug with an actionable gene-drug interaction and needs the result for that decision. Medicaid and commercial coverage vary by state and plan. We verify each patient's coverage before testing.

Medicare, when criteria are metMedicaid & Medi-Cal, varies by stateCommercial, varies by plan
About our PGx test
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Three quick steps. A program specialist follows up with a recommended workflow, materials and a go-live timeline.

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Step 1 of 3Your organization

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STEP 1We review your request

A specialist reads your answers before reaching out.

STEP 2A short discovery call

We learn your workflow, patient population and goals.

STEP 3Your program plan

Recommended workflow, kits and materials, and a go-live timeline.

Questions

Frequently asked

What is pharmacogenomic (PGx) testing?

A PGx test reads genes that control how your body activates and clears medications. Providers use the results to choose drugs and doses that are more likely to work and less likely to cause side effects.

How is the sample collected?

With a simple cheek swab. No needles or blood draw. It can be done in a pharmacy, physician office, hospital unit or at a resident's bedside.

How long do results take?

Typically 5–7 days after the lab receives the specimen. SNF programs receive results by encrypted email or fax within 5–10 business days.

Is it covered by insurance?

Medicare covers PGx testing when a clinician is considering or using a specific drug with an actionable gene-drug interaction and needs the result for that decision. Medicaid and commercial coverage vary by state and plan. We verify coverage first and confirm any cost with the patient in advance.

Does the test need to be repeated?

No. Your genes don't change, so one test can guide medication decisions for life.