Your DNA can play a role in how medications work for you and your body. PGx testing helps your provider understand how you may respond to certain medications, like GLP-1 therapies, so treatment decisions can be more personalized to you and your wellness.
PGx testing helps healthcare providers understand how your genetic makeup may influence your response to certain medications.
We analyze specific genetic markers that affect medication metabolism
Receive detailed results tailored to your genetic profile
Help your provider find the right medication, at the right dose
Simple. Informative. Personalized.
PGx testing can support safer, more effective treatment by helping identify how your body may respond to certain medications.
Identify medications that may work better based on how your body processes them.
Help reduce the risk of adverse drug reactions or poor medication tolerance.
Some patients may need different dosing depending on how quickly their body metabolizes medications.
Support more personalized prescribing decisions using genetic information alongside clinical judgment.
Especially useful for patients starting new therapies or those who have had limited success with multiple medications.
Pharmacogenomics is particularly relevant for mental health medications, as genetic variations can significantly impact how patients respond to antidepressants and antipsychotics.
Genetic differences can affect how quickly your body processes certain antidepressants, which may influence side effects, drug levels, or how well a medication works for you.
PGx testing may help providers make more informed decisions when prescribing, potentially reducing trial-and-error periods and improving treatment outcomes.
PGx testing may be useful for people who want a more personalized approach to medication therapy.
The process is simple and designed to fit into your care plan.
A simple sample is collected according to the testing process.
Your sample is analyzed to identify genetic markers related to medication response.
A comprehensive report is generated showing relevant drug-gene interaction information.
Your healthcare provider uses the results to guide personalized treatment decisions.
Explore examples of medication groups where PGx information may be clinically useful.
Examples: Sertraline, Citalopram, Escitalopram, Fluoxetine, Paroxetine, Venlafaxine, Duloxetine, Amitriptyline, Nortriptyline, Aripiprazole
Why PGx may matter: Genetic differences can affect how quickly your body processes certain antidepressants and antipsychotics, which may influence side effects, drug levels, or how well a medication works.
Examples: Codeine, Tramadol, Hydrocodone, Oxycodone, certain NSAID-related pathways depending on panel design
Why PGx may matter: Some pain medications need to be metabolized into active forms. Genetic differences may affect how well the medication works or the risk of side effects.
Examples: Clopidogrel, Warfarin, certain statin-related pathways depending on test panel
Why PGx may matter: Genetic variation may influence drug activation, effectiveness, or bleeding/clotting risk for some cardiovascular therapies.
Examples: Certain proton pump inhibitors and related GI medications
Why PGx may matter: Metabolism differences may affect medication levels and how well treatment works.
Examples: Selected neurologic or ADHD-related medications depending on panel content
Why PGx may matter: Genetic markers may help explain different responses, tolerability issues, or dosing considerations.
Final medication list should match the exact PGx panel and client-approved content.
PGx testing is available by order of a licensed healthcare provider.
PGx reports are designed to support clinically informed decision-making.
PGx results should always be interpreted by a qualified healthcare professional in the context of the patient's medical history, medications, and treatment goals.
Our testing process is built to support reliable and clinically meaningful results.
Ask your healthcare provider whether PGx testing may be appropriate for you.
