Pharmacogenomic (PGx) testing
Pharmacogenetic (PGx) testing analyzes how your unique genetic makeup influences the way you metabolize and respond to medications. Unlike traditional prescribing, PGx testing helps clinicians tailor drug choice and dosage to each individual, reducing adverse reactions and improving therapeutic effectiveness. By identifying key genetic variations that affect drug metabolism, transport, and receptor interaction, PGx testing supports safer, more precise treatment decisions across multiple therapeutic areas.
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Why PGx Testing Matters?
Reduce trial and error prescribing
By identifying poor, normal, or rapid drug metabolism and guiding precise medication selection.
Minimize adverse drug reactions (ADRs)
And improve safety by uncovering genetic risk factors that affect drug response.
Optimize therapeutic outcomes
across
across
Pain management, psychiatry, cardiology, gastroenterology, and complex polypharmacy regimens.
How PGx Testing Works?
Sample Collection:
Cheek swab or blood sample is taken.- Metabolism Classification: Determines if you are a poor, intermediate, normal, rapid, or ultra rapid metabolizer.
- Clinician Support:
Report helps doctors make personalized prescribing decisions.
DNA Extraction:
DNA is isolated from the collected sample.
DNA is isolated from the collected sample.
Drug Gene Insights: Identifies how your genes affect specific medications.
Optimized Therapy:
Supports safer, more effective medication plans.
Supports safer, more effective medication plans.
- Genetic Analysis:
Genes affecting drug metabolism, transport, and targets are tested. - Actionable Report:
Provides clear guidance on dosage or alternative drugs.
Reduced Side Effects:
Helps prevent adverse drug reactions.
Helps prevent adverse drug reactions.