Your Tool for PGx Enhanced Care
Mitigate Adverse Drug Events
Effortless Integration Into Your Existing Workflow
We make it easy to personalize treatment and integrate with your EMR/EHR systems with 4 EASY STEPS!
1. CONSENT AND COLLECTION:
Patient consents, provider collects DNA via easy cheek swab.
3. ANALYSIS:
We analyze the DNA, checking for genetic variants that cause adverse medication responses.
2. PROCESSING:
Sample sent to our CLIA-certified lab for precise DNA extraction.
4. RESULTS:
PDF report is generated, accessible via EHR and our interactive portal.
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One Swab, Endless Insights
The journey doesn't end after the initial report. Through our portal, healthcare providers can regularly reference the data, using it to shape personalized care as the patient's needs evolve. Embracing new pharmacogenomics research, our expanding portal fuels an informed, personalized health journey.
What PGx Testing Can Tell Us
As a healthcare provider, understanding a patient's metabolism offers a wealth of knowledge that can enhance therapeutic efficacy and mitigate drug-related risks. Here's how:
Toxicity
A slow metabolizer may have excessive amounts of a drug build-up in their system, potentially resulting in adverse reactions.
Lack of Efficacy
A fast metabolizer may not absorb enough of a drug into their bloodstream to achieve a therapeutic effect.
Hypersensitivity
Normal drug amounts can trigger severe reactions in individuals who have hypersensitivity to certain medications.
Therapeutic Applications of PGx Testing
Understanding the metabolic pathways can aid in the personalized treatment and management of several conditions.
Below, we highlight some medical categories and corresponding drug classes where certain medications can be guided by PGx insights.