Educational • Informational • Non-Diagnostic

Tenacity+ Genomic Solutions is a CAP-accredited precision genomics organization focused on advancing pharmacogenomics (PGx)–based insights and clinical decision support. We help clinicians, researchers, and partners better understand how genetic variation may influence medication metabolism, response, and tolerability.

Our services are designed to support education, research, and informed clinical discussion—not to diagnose disease or direct medical treatment.y decision we make is shaped by a clear sense of purpose. Our journey has been anything but ordinary. Through every step, we've focused on staying true to our values and making space for thoughtful, lasting work.

What Tenacity+ Provides

Tenacity+ focuses on the development and delivery of high-quality genetic information and interpretive insights related to medication response.

Our work includes:

Targeted gene profiling related to drug metabolism and transport
Evidence-based interpretation grounded in peer-reviewed literature
Structured genomic insights to support education and clinical discussion
Support for research, innovation, and healthcare professional learning

All outputs are non-diagnostic and are not intended to replace clinical assessment or medical decision-making.

What Is Pharmacogenomics (PGx)?

Pharmacogenomics (PGx) is the study of how genetic differences can influence the way individuals process and respond to medications. Scientific evidence has shown that certain genetic variants may affect drug metabolism, transport, and sensitivity, contributing to variability in efficacy and adverse effects.

PGx insights can help support thoughtful, individualized medication discussions when used alongside clinical judgment and other patient-specific factors.

Who We Support

Tenacity+ collaborates with healthcare professionals and partners across multiple care areas where medication optimization and polypharmacy considerations are common, including:

Mental health and psychiatry
Primary care and internal medicine
Oncology and specialty care
Pain management
Chronic disease management

Our goal is to help stakeholders integrate genomic awareness into patient-centered conversations responsibly and compliantly.

Did you know

50%

According to the Psychiatric Clinics of North America, up to 50% of antidepressant prescriptions fail because the dose or drug is wrong for that person’s genes. Stop switching pills every few months — get the right medication from day one.

of prescriptions
fail

30-50%

Patients who use PGx testing need 30–50% fewer dose changes and experience 40% fewer adverse reactions, and support "less trial, fewer errors" by minimizing reactive changes.

fewer dose changes
with PGx

40%

According to a study by the National Institutes of Health, 4 out of 10 patients are on
a medication today that won’t work properly — or will cause extra side effects — because of their DNA. Find your perfect match on the first try.

of medications don´t
work properly

20%

According to the Mayo Clinic, 1 in 5 serious side effects and hospital visits from medications are
completely preventable with a PGx test. Skip the danger. Know before you take them.

of serious side effects
are preventable

Why PGx, and what can it do
for you and your health?

End the trial-and-error with your medications — once and for all.

Our simple DNA test using buccal swab collected at your convenience, reveals how your body processes hundreds of common medications, all in one report.

With our test, you will discover the following

Individualized evaluation:
Discover exactly which drugs work best for your genes, which are likely to cause side effects or fail, whether you need a higher, lower, or standard dose, and which medications you should avoid entirely.

Prescriptions that work:
No more months of switching pills, suffering side effects, or wondering if this one will finally be the right fit.

Medical support:
Your doctor gets clear, evidence-based guidance to prescribe the safest, most effective medication from day one.

PGx Testing kits

Your genes never change. That means one pharmacogenetic (PGx) test gives you a lifelong cheat-sheet for every prescription you’ll ever take, every dose adjustment, every new doctor, and every future health decision. It’s not a one-time result; it’s personalized medicine for life.

And because these gene variants are inherited, getting the whole family tested is one of the smartest things you can do. One simple test for parents, kids, and even grandparents can protect everyone from the same hidden risks (whether it’s your teenager starting antidepressants, Dad on blood thinners, or Grandma’s new pain medication). One family, one set of tests, a lifetime of safer, smarter healthcare for all of you.

Contact us for Family Pricing

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Pharmacogenetic Testing - DNA Testing -

Pharmacogenetic (PGx) testing is just a cheek-swab DNA test that analyzes the genes that control how your body metabolizes medicines.

How it works: You swab the inside of your cheek, send it back, and in a couple of weeks, we compare your DNA to over 200 common medications (painkillers, antidepressants, blood pressure meds, heart drugs, etc.).

What the results tell you (in plain English): You get one easy-to-read report that says, for each drug your doctor might prescribe:

Green / Perfect Fit → “This one should work great for you at the normal dose.”
Yellow / Use with Care → “You’ll probably need a lower or higher dose, or we’ll watch you closely.”
Red / Avoid → “Your body can’t process this safely — it could cause bad side effects or not work at all.”

What you can actually expect after testing

No more months of “let’s try this pill and see.”
Fewer scary side effects and wasted co-pays.
Your doctor finally knows the right drug and the right dose for you from the very first prescription.
Peace of mind that the next medication you take is the one your body was built for.

One test, one time — and you’re done guessing for the rest of your life. That’s it.