What This Test Measures
- Pharmacogenomic (PGx) analysis of how your genes impact drug metabolism
- Identifies potential adverse reactions or inefficacies across major medication classes
- Swab collection (buccal) for precise, noninvasive testing
Why It Matters
Medication responses are not one-size-fits-all. The GenomeRx Insight panel provides a comprehensive PGx analysis to help guide treatment decisions across multiple therapeutic areas — including pain management, mental health, cardiovascular, and more. With physician-guided interpretation, you can optimize therapy, reduce side effects, and ensure safer, more effective outcomes.
Collection Method
- Collect sample (instructions included in the test kit)
- Return in the prepaid envelope
- Access results securely in the Boomerang Kits App
- Track and monitor results over time
Genetic Insights for Personalized Medicine
Pharmacogenomic (PGx) analysis of how your genes impact drug metabolism and response
Discover how your unique DNA influences how your body processes medications. Gain a clear view of which treatments are most compatible with your genetic profile.
Identify Risks Before They Arise
Flags potential reduced efficacy, side effects, and dosing sensitivities across common medication classes
Avoid the trial-and-error process. Your report highlights potential risks so your provider can tailor medications safely and effectively.
Actionable Guidance for Care Decisions
Supports decision-making for mental health, pain, cardiovascular, and more
Receive a clear, physician-friendly report that guides evidence-based decisions for multiple health areas — from psychiatry to primary care.
Simple, Fast, and Non-Invasive
Non-invasive buccal swab; results typically 24–48 hours after lab receipt
Collect your sample at home in seconds — no needles, no blood. Track progress online and receive results within 2 days of lab processing.
Genetic Insights for Personalized Medicine
Pharmacogenomic (PGx) analysis of how your genes impact drug metabolism and response
Discover how your unique DNA influences how your body processes medications. Gain a clear view of which treatments are most compatible with your genetic profile.
Identify Risks Before They Arise
Flags potential reduced efficacy, side effects, and dosing sensitivities across common medication classes
Avoid the trial-and-error process. Your report highlights potential risks so your provider can tailor medications safely and effectively.
Actionable Guidance for Care Decisions
Supports decision-making for mental health, pain, cardiovascular, and more
Receive a clear, physician-friendly report that guides evidence-based decisions for multiple health areas — from psychiatry to primary care.
Simple, Fast, and Non-Invasive
Non-invasive buccal swab; results typically 24–48 hours after lab receipt
Collect your sample at home in seconds — no needles, no blood. Track progress online and receive results within 2 days of lab processing.
Frequently Asked Questions
What’s included, how to collect, when you’ll see results, and how to use them.
What does this panel measure?
A comprehensive pharmacogenomic (PGx) analysis examining how your genes affect drug metabolism and response across multiple therapeutic areas. It identifies potential inefficacies or adverse reactions to support safer, more effective treatment decisions.
How is this different from traditional testing?
GenomeRx Insight combines advanced genomic sequencing with CLIA-certified precision and secure digital delivery. It transforms complex pharmacogenomic data into actionable insights that empower collaboration between patients and clinicians—without clinic visits or hidden telehealth upsells.
Who benefits most from this panel?
Individuals taking multiple prescriptions, experiencing side effects, or seeking to personalize treatment strategies through precision medicine.
How do I collect the sample?
Simple at-home buccal (cheek) swab collection. Follow the insert or in-app guide; it takes only minutes. Place the swab in the provided transport tube, seal securely, and return it using the prepaid mailer.
How long until I see my results?
Typically within 24–48 hours after our laboratory receives your sample, you’ll receive a secure notification in the Boomerang Kits App.
Where do I view my results?
Your results are delivered digitally and securely in your Boomerang Kits App, accessible only to you through your personalized login.
Is my data private?
Your genomic data is encrypted, HIPAA-compliant, and never shared without your explicit consent. Boomerang Laboratories maintains the highest standards of data protection and privacy in compliance with all applicable U.S. privacy laws.
How should I use these results?
Review your GenomeRx Insight findings with your healthcare provider to optimize therapy and medication safety. Genetic results should always be interpreted within your overall medical context.
How do I return my sample?
Use the prepaid mailer included with your kit. Drop it at any postal location the same day you collect your sample to ensure prompt delivery.
What if my sample can’t be processed?
If your sample is insufficient or cannot be analyzed, you’ll be notified and sent a complimentary replacement kit at no cost.
Is this covered by insurance?
Boomerang Kits are consumer-initiated and not typically billed to insurance. HSA/FSA funds may apply depending on your plan.
What other panels complement this one?
Mental Health Genomic and ADHD Genomic Panels for a unified view of medication response and neurochemical balance.
Is this a diagnostic test?
No. This is a genomic screening intended for informational purposes. Genetic results reflect predispositions, not guarantees. Environmental and lifestyle factors also influence outcomes.