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Medication Check (PGx testing)

Explains how your DNA affects your body’s response to medications. It covers 50 drugs, offering guidance on whether you can follow standard precautions or should exercise extra caution. View sample report.
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Proven track record: 3+ million analyses delivered

Trusted by 200,000+ users & 2,000+ doctors

Proven track record: 3+ million analyses delivered

Demonstrates how gene variants affect drug metabolism
Covers over 50 medications
Insights based on CPIC and FDA guidelines
Dosing and side effect information

Product features

Note: To generate your personalized report, purchase a SelfDecode DNA kit. If you already have one, you’re ready to proceed.

 

Are you uncertain about how well standard dosages of certain drugs will work for you? Do you want to know whether you’re more prone to adverse effects from common pain relievers, anticoagulants, or antidepressants? The Medication Check (PGx testing) report provides clarity by analyzing your genetic variants and showing how they may influence your reaction to over 50 medications.

 

Understanding Your Genetic Response to Medications

Unlike a one-size-fits-all approach, this genetic test highlights if you might need a lower dose, an alternative drug, or simply more vigilant monitoring. Each gene-drug interaction is explained in an accessible format, so you’ll see at a glance whether you fall under “Standard Precautions” or “Use With Caution.” If the report flags a potential for adverse events, it indicates where adjustments may be warranted – information you can share with your doctor or pharmacist.

This report analyzes your genetic variants to predict how your body might respond to these 50 medications:

  1. Anesthesiology
      • Anesthetics: Volatile Anesthetics (Desflurane, Enflurane, Halothane, Isoflurane, Methoxyflurane, Sevoflurane)
      • Skeletal Muscle Relaxants: Succinylcholine
  • Cardiovascular
      • Antiplatelets & Anticoagulants: Acenocoumarol, Clopidogrel, Phenprocoumon, Warfarin
      • Statins: Atorvastatin, Fluvastatin, Lovastatin, Pitavastatin, Pravastatin, Rosuvastatin, Simvastatin
  • Gastrointestinal
      • Proton Pump Inhibitors: Dexlansoprazole, Lansoprazole, Omeprazole, Pantoprazole, Rabeprazole
  • Immunology, Rheumatology & Oncology
      • Antihyperuricemic & Antigout Agents: Allopurinol
      • Antimetabolites: Capecitabine, Fluorouracil, Mercaptopurine, Tegafur
      • Immunosuppressants: Azathioprine, Methotrexate, Siponimod, Tacrolimus
  • Infections
      • Antifungals: Voriconazole
      • Antivirals: Efavirenz, Nevirapine, Triple therapy (peginterferon alfa-2a/b & ribavirin)
  • Pain
      • NSAIDs: Celecoxib, Flurbiprofen, Ibuprofen, Lornoxicam, Meloxicam, Piroxicam, Tenoxicam
      • Opioids: Methadone
  • Psychotropic
    • Antidepressants: Amitriptyline, Bupropion, Citalopram, Clomipramine, Doxepin, Escitalopram, Imipramine, Sertraline, Trimipramine
    • Antiepileptics: Phenytoin
    • Antipsychotics: Quetiapine

 

Evidence-Based Insights

By consolidating guidelines from leading pharmacogenomics authorities, the report allows you to see where research-based consensus supports certain dosing adjustments. This evidence-based approach empowers you to collaborate with your healthcare team in tailoring treatments more precisely.

 

Reducing Uncertainty

Even if no major genetic red flags appear, the Drug Check (PGx Test) Report reduces guesswork. You’ll know your baseline risk for things like muscle pain from certain statins or reduced effectiveness of certain proton pump inhibitors (acid reducers), enhancing your confidence in treatment choices.

 

Important Note

This report is for informational purposes only. It does not replace professional medical advice, and you should always consult with a qualified healthcare provider before making medication decisions. Genetics is just one piece of the puzzle – factors like age, body weight, and other medications also play a role in how your body handles drugs.

WHY SELFDECODE?

Empowering Your Well-being Journey

This personalized health report is powered by SelfDecode's cutting-edge AI technology, designed to unlock a deeper understanding of your health potential. We're committed to providing you with the most accurate and actionable insights to guide your well-being journey.

Most Accurate
Polygenic Risk Scoring

We leverage cutting-edge algorithms and analyze a massive dataset of 2 million people to deliver the most precise assessment of your genetic health predispositions. Our advanced approach takes into account your ancestry - which is often overlooked by other methods - to provide you with the most accurate risk assessment. This ensures that the risk scores you receive are based on the latest scientific evidence and are truly personalized to your genetic makeup.

Cutting-Edge AI &
Machine Learning

We have invested 20 million dollars developing our AI and machine learning models. Our patent-pending technology provides you with the most personalized health insights and recommendations by taking into account your unique DNA, lifestyle, labs, symptoms, conditions and health goals. This empowers you to make informed decisions tailored to your specific needs.

Analyzes 200 Million Variants & Sophisticated Recommendation Engine

We go beyond the basics by analyzing a staggering 200 million genetic variants to provide the most comprehensive picture of your health potential. Our sophisticated recommendation engine leverages this deep analysis to provide personalized and actionable insights to optimize your well-being journey.

Built by Leading
Scientists & Engineers

A dedicated team of over 60 scientists and engineers is continuously innovating and developing our technology, ensuring it remains at the forefront of personalized health.

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  1. Sid

    Being diagnosed with cancer was overwhelming. This report’s analysis of my DPYD and UGT1A1 gene variants helped explain my heightened sensitivity to chemotherapy drugs. It enabled my oncology team to personalize treatment dosages to minimize side effects while maintaining efficacy. Having this genetic information was empowering and crucial during a tough time.

  2. Lauren

    As a parent, I want to ensure my kids’ future health. This pharmacogenomics report helped me understand how their genetic makeup influences medication responses, especially related to pain and allergy meds. The actionable advice on what to avoid and what works best is a relief. The educational graphics and gene summaries made it accessible even without a science background.

  3. Murat

    After struggling with side effects from standard anti epileptic drugs, this report identified variations in my CYP3A5 and ABCB1 genes that impact drug clearance. The recommendations helped my neurologist select better tolerated medications. The in depth yet plain language explanations truly empowered me to participate actively in managing my condition.

  4. Hayley

    I was concerned about adverse drug reactions due to family history. This Pharmacogenomics report provided comprehensive insights into my genes related to drug metabolism including VKORC1 and CYP4F2 affecting blood thinner sensitivity. The recommended monitoring plan is straightforward and gives me confidence in my treatment. The report balances technical detail with clear, supportive guidance perfectly.

  5. Angel

    Living with rheumatoid arthritis, I’ve had varied responses to medications. This report’s analysis of my TPMT gene variant clarified why I had reactions to certain immunosuppressants. Understanding these pharmacogenetic insights allowed my rheumatologist to adjust my therapy safely. The report’s detailed but accessible format is ideal for patients wanting to engage deeply with their health data.

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