
Bringing Pharmacogenomics into Primary Care
Pharmacogenomic testing is moving beyond specialty clinics. Here's how primary care providers can start using it to guide prescribing decisions.
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Pharmacogenomic testing is moving beyond specialty clinics. Here's how primary care providers can start using it to guide prescribing decisions.
Pharmacogenomic testing analyzes how a patient's genetics affect their metabolism of common medications, informing safer, more effective prescribing.
What was once ordered mainly by oncologists and psychiatrists is now finding a place in routine primary care visits, particularly ahead of long-term prescriptions.

A single panel, ordered once, can inform prescribing decisions across a patient's lifetime — not just the medication in front of you today.

Primary care providers are increasingly ordering pharmacogenomic panels ahead of starting patients on psychiatric or pain management medications, where metabolizer status has an outsized effect on both efficacy and side-effect risk.
Clear, actionable reporting is critical to making this testing usable in a busy primary care workflow — a report is only as good as how quickly a provider can translate it into a prescribing decision at the point of care.
Dr. Marcus Ide
MD, Clinical Genetics
Dr. Ide advises primary care networks on integrating genomic testing into everyday prescribing workflows.
More clinical perspectives and testing guidance from our medical and scientific teams.

