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Pharmacogenomics - how your genes affect 112+ medications.

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Wider screening than the NHS heel-prick, from a cheek swab.

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Medication Check

Find out how your body processes 112+ medications across 14 therapy areas - so you and your doctor can choose the right drug, at the right dose, first time.

Medication Check from £210

Genes analysed:

CYP2D6
CYP2C19
CYP2C9
CYP3A4
CYP3A5
SLCO1B1
VKORC1
DPYD
TPMT
+100 more medications
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PKD Genetic Panel from £930
112+

Medications

Screened across 14 therapy areas

14

Therapy areas

Mental health, pain, heart, cancer and more

~4 wks

Typical turnaround

GP-reviewed report

£210

One-off test

Valid for life - your DNA doesn't change

Table of contents

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Cancer
Breast Cancer
Book now £930

What is a pharmacogenomic test?

Pharmacogenomics looks at how your genes affect the way your body responds to medicines. Small differences in your drug-metabolising genes can mean a standard dose is too strong, too weak, or more likely to cause side effects for you. A one-off test reads those genes so prescribing can be tailored to you - not the average patient.

We analyse the genes that matter most for drug response: the cytochrome P450 enzymes (CYP2D6, CYP2C19, CYP2C9, CYP3A4/5), the drug transporter SLCO1B1, and drug targets such as VKORC1 for warfarin. Around 5–10% of people of European ancestry are CYP2D6 “poor metabolisers”, for example - your report places you in one of four clear categories (poor, intermediate, normal, or rapid/ultra-rapid).

What it covers - 112 medications, 14 therapy areas

Your report spans the medicines where genetics most affects safety and effectiveness:

  • Mental health - 25 drugs (SSRIs, SNRIs, tricyclics, antipsychotics)
  • Pain relief - 12 drugs (codeine, tramadol, oxycodone)
  • Heart - 9 drugs (warfarin, clopidogrel, carvedilol)
  • Cholesterol - 7 statins
  • Cancer - 11 drugs (tamoxifen, irinotecan, capecitabine)
  • Infection - 12 drugs (antiretrovirals, antivirals)
  • And more - digestive, immune, nervous system, diabetes, bone & joint, ADHD, chest

How it works

  1. Talk to a clinician - start with a free 30-minute consultation with a GP to confirm the test is right for you.
  2. Consent & collect - complete your online consent, then collect your sample at home with a simple cheek swab. No clinic visit, no fasting.
  3. Results & follow-up - your report is reviewed by a GP and shared securely, with a complimentary video appointment to talk it through if needed.

Why Jeen

  • Same lab and technology as major UK reseller programmes - analysed at Eurofins UK on Illumina pharmacogenomic arrays (CE-IVD, ISO 15189/17025/13485, CQC-registered).
  • No pre-test delay - your kit ships the day you order.
  • A lifetime-valid report - your genome doesn't change, so you can reuse it for any future prescription.
  • Independent and private - results are never shared with UK health insurers, and your sample is destroyed after your report is delivered.
  • No fasting, and no need to stop your current medication.

Disclaimer! The information provided in this article is for educational purposes only. It is not a substitute for professional medical advice. Always consult your doctor or a qualified healthcare provider for advice on medical conditions or treatments. Sources used: NCBI, UK Kindney Association, NHS.

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What do we test for?

Know your genes, protect your future. Over 5,000 diseases are linked to genetic mutations. Early insights through genetic testing can help with prevention, early detection and personalised healthcare decisions.

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Frequently Asked Questions

Do I need to stop my medication?

No. Take your prescribed medication exactly as your doctor recommended - your current prescriptions do not affect the result.

How long do results last?

Forever. Your DNA stays the same throughout your life, so the variants we report are stable - your report is valid for life.

Will my insurer get access to the results?

No. We do not share genetic-test results with UK health insurers; the test is independent and not insurer-tied.

What happens to my sample?

Your sample is destroyed after the analysis is complete and your report has been delivered.

Who can take the test?

UK residents aged 18 and over. It is not suitable if you have had a transplant or a blood transfusion within the last 4 weeks.

What is pharmacogenomic (PGx) testing?

Pharmacogenomics is the study of how your genes affect the way your body responds to medicines. A pharmacogenomic test reads the drug-metabolising genes that determine whether a standard dose is likely to be too strong, too weak or more likely to cause side effects for you - so your prescriber can choose the right medication and dose first time, rather than by trial and error.

Which medications does the test cover?

The test screens 112+ medications across 14 therapy areas, focusing on the drugs where genetics most affects safety and effectiveness. These include antidepressants and antipsychotics, painkillers such as codeine and tramadol, heart medicines such as warfarin and clopidogrel, statins and several cancer therapies. It reads the key genes for drug response, including CYP2D6, CYP2C19, CYP2C9, CYP3A4/5, SLCO1B1, VKORC1, DPYD and TPMT.

How much does the Medication Check test cost?

The pharmacogenomic test is a one-off £210, which covers your at-home cheek-swab kit, analysis of all 112+ medications, a GP-reviewed report and a complimentary GP video appointment if you need one. Because your DNA does not change, the report is valid for life - there is nothing more to pay for future prescriptions.

Will the test tell me exactly which medication to take?

No - and it is not meant to. The report tells you and your prescriber how you are likely to process particular medicines (for example, whether you are a poor, normal or rapid metaboliser), so they can use that alongside your medical history to choose the most suitable drug and dose. Any prescribing decision always rests with your doctor.

How do I take the test, and how long do results take?

You collect your sample at home with a simple cheek swab - no blood, no clinic visit and no fasting. Results are typically ready in about four weeks and are reviewed by a GP, who can arrange a video appointment to talk them through if needed.

Sources & references

The statistics and clinical claims on this page are supported by the following authoritative sources.

  • NCBI / PMC
  • NCBI

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