Pharmacogenomics Testing

Pharmacogenomics (often abbreviated PGx) is the study of how a person’s genes affect their response to medications. It combines pharmacology (the science of drugs) and genomics (the study of genes and their functions) to understand why certain medications work well for some people but not for others, or why some patients experience serious side effects while others do not.

1. People who take multiple medications (polypharmacy).

2. Those with a history of side effects or poor response to meds.

3. Patients starting antidepressants, pain meds, blood thinners, or cancer therapies — areas where PGx is especially valuable.

4. Anyone who wants a personalized approach to their healthcare.

1. Safer Medications - Your DNA can reveal if a drug might cause serious side effects for you. PGx testing helps your doctor choose safer options.

2. Faster Results - Skip the “trial-and-error” of finding the right prescription. Your genetics can guide your doctor toward medicines that are more likely to work the first time.

3. Personalized Dosing - Some people break down medicines too quickly, others too slowly. PGx shows how your body processes medications so you get the right dose.

4. One Test = Lifetime Value - Your genes don’t change. A single PGx test can give useful insights for your prescriptions for the rest of your life.

5. Peace of Mind - Knowing your medications are tailored to your DNA means fewer side effects, better outcomes, and more confidence in your treatment plan.