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AchieveDx pharmacogenomic testing

One cheek swab shows how a patient's genetics affect their response to medications across cardiology, mental health, pain management and more.

See a sample report
SpecimenBuccal swab
Turnaround from lab receipt5–7 days
Medications77
Repeat testingTypically not needed
AchieveDx PGx sample collection kit box: One quick test. Lifelong personalized medication guidance.
The collection kit

One box, one swab, one lifetime of guidance

  • Swab and step-by-step instructions inside the box
  • Label with patient name, date of birth and collection date
  • Ship the day of collection, or refrigerate until it ships
  • Seal the specimen in the same box and ship it to the lab
Why AchieveDx PGx

The right medication, at the right dose, at the right time

A patient's genetic profile doesn't change. Their medication list does. One test gives prescribers drug-gene insight they can use for future prescriptions.

  1. 01

    Less trial and error

    Can help reduce failed medications and the risk of adverse drug reactions.

  2. 02

    Safer prescribing

    Flags drug-gene interactions and genetic risk for adverse reactions.

  3. 03

    Better-tolerated choices

    Helps prescribers choose therapies patients are more likely to tolerate.

  4. 04

    Readable reports

    Clear, color-coded results plus a pharmacist-written summary.

Clinical applications

Where PGx changes prescribing

Cardiology

Antiplatelets (clopidogrel)StatinsBeta-blockersWarfarin

Supports drug selection for antiplatelets and statins.

Mental health

SSRIs and SNRIsTricyclicsAntipsychoticsADHD medications

Supports antidepressant and antipsychotic selection.

Pain management

Opioids (codeine, tramadol)NSAIDsNeuropathic pain agents

Helps identify patients unlikely to benefit from codeine or tramadol.

Primary & complex care

PolypharmacyChronic diseaseGI, neurology, oncology

Supports prescribing decisions in polypharmacy.

Medications on the report

Every medication on the report

Browse the full list, filter by therapeutic area or search by generic or brand name. Select a medication to see how a result can guide prescribing.

Medication list from the AchieveDx PGx report. Whether a result changes therapy depends on the patient's genotype and full clinical picture. For information only, not medical advice.

When to test

Key moments in the patient's care

PGx testing fits at four points in a patient's treatment. Test once, and the results can inform future prescribing.

  1. Moment 1

    Therapy initiation

    Avoid trial and error from the start.

  2. Moment 2

    During treatment

    Address side effects, poor response or adherence problems.

  3. Moment 3

    Dose optimization

    Guide dosing, especially for narrow therapeutic index drugs.

  4. Moment 4

    Therapy failure

    Find genetic factors behind a poor response.

Establishing medical necessity

For Medicare (MolDX), document these in the order. A history of side effects, therapeutic failure or dose instability supports the record but isn't enough on its own. Testing isn't covered based on a diagnosis alone.

  • The specific drug being considered or currently used
  • That it has an actionable gene-drug interaction (CPIC level A/B or FDA labeling)
  • How the result will guide dosing or drug selection
  • That non-genetic factors were also considered
Guideline support

Built on established guidance

Recommendations on the AchieveDx report reference these guideline and labeling sources.

CPICClinical Pharmacogenetics Implementation Consortium

Evidence-based prescribing recommendations for actionable drug-gene pairs.14

FDAU.S. Food and Drug Administration

Pharmacogenomic information in the labeling of hundreds of medications.15

DPWGDutch Pharmacogenetics Working Group

Guidelines used to guide prescribing in the PREPARE trial.1,19

NICENational Institute for Health and Care Excellence (UK)

Recommends CYP2C19 testing to guide clopidogrel after ischaemic stroke or TIA.20

Organizations are listed as reference sources and do not endorse AchieveDx.

Evidence by specialty

Where the data is strongest

CPIC has published 29 guidelines covering more than 160 drugs and 35 genes (as of October 2025), and the FDA maintains a table of pharmacogenetic associations for drugs with labeling or evidence of gene-drug effects.14,16

Cardiology1 in 4+people of European or African ancestry, and more than half of East Asians, carry at least one CYP2C19 no-function allele10

Clopidogrel must be activated by CYP2C19, so carriers may get less antiplatelet effect and have a higher risk of cardiovascular events. A 2024 American Heart Association scientific statement concluded that the evidence to date supports CYP2C19 testing before oral P2Y12 inhibitors in ACS and PCI.

Lee CR, et al. Clin Pharmacol Ther, 2022 (CPIC); Pereira NL, et al. Circulation, 2024 (AHA)9

Psychiatry1.46×more likely to reach depression remission with PGx-guided care, across the 10 randomized trials in a 2022 meta-analysis13

About 13% of U.S. adults used an antidepressant in the past 30 days (2015–2018).11 In the VA's PRIME trial of 1,944 veterans, PGx-guided patients were prescribed fewer medications with predicted gene-drug interactions.12

Brown LC, et al. Clin Pharmacol Ther, 2022; Oslin DW, et al. JAMA, 2022

Pain managementFDAboxed warning: deaths in children given codeine, many of them CYP2D6 ultrarapid metabolizers

Ultrarapid metabolizers convert codeine to morphine too quickly, which can cause life-threatening breathing problems. Poor metabolizers get little pain relief.

Codeine FDA prescribing information17

Examples of FDA drug labeling

DrugGene / phenotypeFDA label guidance
ClopidogrelCYP2C19 poorBoxed warning Consider another P2Y12 inhibitor in CYP2C19 poor metabolizers.
CodeineCYP2D6 ultrarapidBoxed warning Life-threatening respiratory depression and death in children who received codeine, many of whom were ultrarapid metabolizers.
CitalopramCYP2C19 poorDose limit Maximum dose of 20 mg/day in CYP2C19 poor metabolizers.

Sources: FDA prescribing information for each drug; CPIC; FDA Table of Pharmacogenetic Associations.14,16,17

Figures come from published studies of PGx-guided care in other programs and populations. They are not results of AchieveDx's test. See references.

Build your testing program

Tell us about your organization.

Three quick steps. A program specialist follows up with a recommended workflow, materials and a go-live timeline.

Your program so farNothing yet

Your organization and the tests you pick will show here.

Prefer to talk now?
(618) 224-4383
info@achievedx.com
Step 1 of 3Your organization

What kind of organization are you?

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.