Pharmacogenetic
(PGx) Testing
Genetic information should be essential when prescribing
Gain a better understanding of the patient’s unique genetic profile to reduce the painful process of trial and error and interaction risk.
270+
medications contain FDA warnings, dosage recommendations or drug-drug interaction guidance based on specific gene variants.9
95%
- Food and Drug Administration
Personalize medication plans with ease
Genomind’s pharmacogenetic testing makes it easy for you and your patient to access these critical treatment insights without compromising accuracy or depth of information.
Access comprehensive genetic insights of 24 genes to assess over 800 medications in our Precision Medicine Software: GenMedProâ„¢
Enjoy fast, easy and accurate processing – painless cheek swab collection and results in 3-5 days or less with a 99.9% laboratory accuracy
Seamlessly incorporate into your care model with flexible collection options – keep test kits on hand or send directly to patients
Offer payment options that work for your patients – HSA/FSA eligible, flexible payment plans, and patient assistance
How pharmacogenetic testing works
Ordering, tracking, and status updates related to your testing results can be easily accessed by logging on to our Precision Health Platform after you register with Genomind.
Customized report views to fit your approach to treatment
Pharmacodynamic
Gene Variation Report
Assess 15 pharmacodynamic (PD) gene results to understand how their genotype may affect tolerability and/or likelihood of responding to specific therapeutic options.
Pharmacokinetic
Gene Variation Report
Evaluate 9 pharmacokinetic (PK) gene results to understand how their genotype may affect drug metabolism and absorption of certain drugs.
Gene-Drug Interaction
Summary Report
Understand how your patient’s genetic profile interacts with commonly prescribed medications synthesizing both the PK and PD results for each drug. Understand how their genotype may influence biological response, drug absorption, metabolism, or blood-brain barrier penetration.
Diagnosis-Specific
Summary Report
All results are organized into one visually plotted view based on clinical diagnosis. When you’re running short on time – this may be the report view for you!
Test Methodology /
Literature Reference
Easily access descriptions of test methodology, more detailed information regarding the genetic variant tests (i.e. single-nucleotide polymorphisms), and literature references.
Patient Drug Metabolism Card
Built on the most up-to-date clinical evidence
As science evolves, so do we. Learn about the evidence the pharmacogenetic testing report was built on and our commitment to staying current.
PGx is the future of medicine. I use it to bring precision to my prescribing. Now, I can more accurately predict adverse drug events, even outside of my specialty. This process builds better relationships with patients and other providers.
Jennifer Reed, FNP-BC, PMHNP-BC
Private Practice Owner, Board Certified in Family Practice and Psychiatric Mental Health
