Pharmacogenomic (PGx) Panel
Also known as: Drug metabolism test · Pharmacogenetics test · Medication response DNA test
Genetic analysis of drug-metabolising enzymes to guide safer, more effective medication selection and dosing.
Reviewed by a certified medical doctor
This page and the corresponding laboratory report are overseen by an in-house clinician to ensure medical accuracy and patient safety.
- Reviewing doctorDr. Yusuf Abdullahi, MBBS, FMCPath
- Clinical titleConsultant Chemical Pathologist
- MDCN registrationMDCN/2010/52118
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Last clinical review
30 Jul 2026
Next review due 30 Jul 2027
“Two patients can respond very differently to the same drug. Pharmacogenomics helps explain why, and allows clinicians to personalise prescribing rather than rely on trial and error.”
Dr. Yusuf Abdullahi, MBBS, FMCPath
When is this test recommended?
Consider PGx testing if you:
- Have experienced adverse drug reactions or poor response to medication
- Take multiple long-term medications (polypharmacy)
- Are starting a medication with known pharmacogenomic guidance
- Have a family history of unusual drug responses
- Want a preemptive profile to guide future prescribing
How to prepare and how the sample is collected
- Specimen typeBuccal (cheek) swab or EDTA whole blood
- Turnaround14 business days
Patient preparation
No fasting required. Bring a current list of medications you are taking, including doses.
Collection methods
- Painless cheek (buccal) swab — quick, non-invasive and suitable for all ages.
- Venous blood draw — EDTA whole blood, taken by a certified phlebotomist.
- Discreet home collection kit — courier-dispatched nationwide with clear instructions.
How your sample is analysed
Targeted genotyping of key pharmacogenes (including CYP2D6, CYP2C19, CYP2C9, VKORC1, TPMT, DPYD and others) by multiplex PCR and targeted sequencing. Results are interpreted against established clinical guidelines and reported with actionable prescribing considerations.
Platforms & instrumentation
Multiplex PCR genotyping arrays and targeted next-generation sequencing panels with clinical annotation databases.
- Documented standard operating procedures for every assay.
- Internal reference controls run alongside patient samples.
- Participation in external proficiency testing programmes.
- Dual-verification of every result before release.
How you receive your results
Encrypted, password-protected PDF report
Your results are delivered securely as an encrypted, password-protected PDF to your registered email address and WhatsApp. The file is never sent unprotected. Results are issued as an encrypted, password-protected PDF with a clinician-facing interpretation summary. Counseling is available to explain implications.
Opening your report
- The PDF password follows a standard formula based on your personal details.
- Your counselor will confirm the exact password formula before release.
- Need help? Our team can re-issue or reset access on request.
Pre- and post-test counseling
Certified genetic counselors are available before and after your test to explain what the results mean, discuss implications for your family, and guide any next clinical steps.
Common questions about Pharmacogenomic (PGx) Panel
No. PGx results are decision-support information for your clinician. Never change medication without consulting your treating physician.
Yes. Your inherited pharmacogenomic profile does not change over your lifetime, so the result remains useful for future prescribing decisions.
Where to give your sample
Collection at Abuja, Lagos and Kaduna centres, or via home collection kit.