Psychiatric Medication Report

Pharmacogenomic analysis of antidepressants, ADHD medications, and mood stabilizers from your existing DNA data.

What This Report Does

The Psychiatric Medication Report analyzes your CYP2D6 results and CYP2C19 genotypes and maps them against CPIC clinical guidelines for psychiatric medications. These two genes metabolize the majority of commonly prescribed antidepressants, ADHD medications, and antipsychotics.

Your report identifies your metabolizer phenotype for each gene and flags specific medications where your genetics may affect drug metabolism, exposure, or side-effect risk. Results are organized by condition (depression & anxiety, ADHD) and include a clinician pocket summary you can share with your prescriber.

Medications Covered

The report covers psychiatric medications with CPIC-level evidence for CYP2D6 or CYP2C19 drug-gene interactions, including:

  • SSRIs: escitalopram (Lexapro), sertraline (Zoloft), citalopram (Celexa), paroxetine (Paxil), fluoxetine (Prozac), fluvoxamine (Luvox)
  • SNRIs: venlafaxine (Effexor)
  • Tricyclic antidepressants: amitriptyline, nortriptyline, clomipramine, imipramine, desipramine
  • ADHD medications: atomoxetine (Strattera)
  • Antipsychotics: clozapine (Clozaril), flupentixol (Fluanxol)

This list represents medications with current CPIC or DPWG guideline evidence. Coverage may expand as new guidelines are published. For a broader view of CYP2D6-metabolized antidepressants, see our CYP2D6 and antidepressants guide.

How It Works

  1. Upload your DNA data from 23andMe, AncestryDNA, MyHeritage, or FamilyTreeDNA.
  2. Your raw data is analyzed to extract CYP2D6 and CYP2C19 variants and assign star alleles, diplotypes, and metabolizer phenotypes.
  3. Results are mapped to CPIC guidelines for each psychiatric medication, identifying interactions where your genotype may affect drug metabolism.
  4. Your report is generated with a priority dashboard, condition-based groupings, decision table, and clinician pocket summary.

For details on the analysis pipeline, see our methodology page or read about how pharmacogenomic testing works.

See what the report looks like. Preview a complete Psychiatric Medication Report with sample findings for CYP2D6 and CYP2C19.

View sample report · Upload your DNA data

Who This Report Is For

  • People currently taking or considering antidepressants, ADHD medications, or antipsychotics who want to understand how their genetics may affect drug metabolism.
  • People who have experienced side effects or lack of response with psychiatric medications and want to explore whether pharmacogenomics could provide useful context for their prescriber.
  • Anyone with 23andMe, AncestryDNA, or other consumer DNA data who wants to extract pharmacogenomic insights from raw data they already have.

The Genes Behind the Report

The report focuses on two pharmacogenes with the strongest clinical evidence for psychiatric medication metabolism:

  • The CYP2D6 gene — Metabolizes approximately 25% of all prescribed medications, including many antidepressants (fluoxetine, paroxetine, venlafaxine, nortriptyline), antipsychotics (clozapine, flupentixol), and atomoxetine for ADHD.
  • The CYP2C19 gene — The primary metabolic pathway for escitalopram, sertraline, citalopram, and several tricyclic antidepressants including amitriptyline and clomipramine.

Your metabolizer status for each gene determines whether CPIC guidelines flag any psychiatric medications for potential dose adjustments or alternative therapy considerations.

What the Report Includes

  • Risk snapshot: Summary of significant and moderate findings across your psychiatric medication profile.
  • Condition-based groupings: Medications organized by depression & anxiety, ADHD, and other psychiatric indications.
  • Decision table: Each flagged medication with gene, guideline action, and CPIC evidence level.
  • Detailed gene findings: Your CYP2D6 and CYP2C19 diplotypes, activity scores, and phenotype classifications.
  • Clinician pocket summary: A one-page overview formatted for your healthcare provider.

Get your Psychiatric Medication Report. Upload your raw DNA data to see your CYP2D6 and CYP2C19 results mapped to antidepressants, ADHD meds, and antipsychotics.

Upload your data · View sample report · Compare testing options

Limitations

  • This report analyzes CYP2D6 and CYP2C19 only. Other genes and non-genetic factors also influence psychiatric medication response.
  • Consumer genotyping arrays cannot detect gene deletions or duplications, which affect some CYP2D6 phenotype classifications.
  • Pharmacogenomic results do not predict whether a medication will reduce your symptoms. They indicate how your genetics may affect drug metabolism.
  • This is not medical advice. All medication decisions should be made with your healthcare provider. See our full limitations page.

Learn More

Frequently Asked Questions

Which genes are included in the Psychiatric Medication Report?

The report analyzes CYP2D6 and CYP2C19 — the two pharmacogenes with the strongest clinical evidence for psychiatric medication metabolism. Together, these genes cover the majority of CPIC-guideline psychiatric drug-gene interactions.

What medications are covered?

The report covers SSRIs (escitalopram, citalopram, sertraline, paroxetine, fluoxetine, fluvoxamine), SNRIs (venlafaxine), tricyclic antidepressants, ADHD medications (atomoxetine), and antipsychotics (clozapine, flupentixol) — 18 medications with CPIC-level evidence.

Does the report diagnose psychiatric conditions?

No. The report does not diagnose depression, anxiety, ADHD, or any other condition. It analyzes how your genetics may affect the metabolism of psychiatric medications. Diagnosis and treatment decisions are made by your healthcare provider.

Will the report tell me which antidepressant works best for me?

No. Pharmacogenomics identifies how you metabolize specific drugs — not which drug is most effective for your condition. Your prescriber uses pharmacogenomic information alongside clinical factors to guide medication choices.

Can I use 23andMe or AncestryDNA data?

Yes. The report works with raw data from 23andMe, AncestryDNA, MyHeritage, and FamilyTreeDNA. Consumer arrays include many CYP2D6 and CYP2C19 star allele variants, though gene deletions and duplications cannot be detected from array data.

How is this different from GeneSight?

GeneSight requires a prescription, a new cheek swab, and uses a proprietary algorithm. DecodeMyBio uses DNA data you already have, maps results to published CPIC guidelines, and costs $59 with no prescription. See our detailed comparison.

Last reviewed: February 2026 · DecodeMyBio Editorial Team

Medical Disclaimer

DecodeMyBio provides informational pharmacogenomic reports only. This is not medical advice. Always consult your healthcare provider before making medication changes.