Pharmacogenomic (PGx) testing is moving from specialty clinics into everyday prescribing conversations. This page gives physicians, pharmacists, and nurse practitioners a clear picture of what our panel covers, how the process works for patients, and what a report looks like — plus a downloadable one-page kit you can print or share.
Many patients try two or three medications before finding one that works. PGx variants in metabolism and transport genes are one factor that can help explain those differences in response and tolerability.
Each report pairs the patient's genotypes with plain-language, medication-specific summaries referencing established clinical guideline evidence — built to be read in minutes, not hours.
Optional board-certified genetic counseling sessions mean patients come to your visit with informed questions, structured findings, and realistic expectations about what PGx does and doesn't tell them.
The NextGen PGx Complete PGx panel examines well-studied genes involved in drug metabolism, transport, and hypersensitivity risk. Below is a summary of coverage; the full panel and reporting details are included in the sample report.
Your patient orders online at nextgenpgx.com — no clinic paperwork, no insurance claims, no staff time.
A cheek-swab kit ships to their door with a prepaid return envelope and clear instructions.
The report lands in a secure, HIPAA-compliant patient portal, with medication-specific summaries the patient can share with you.
You review the findings with the patient alongside clinical factors. Optional genetic counseling is available before or after the visit.
Review a de-identified sample report, or browse our white papers on the clinical evidence.