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PGx FOR NEUROLOGY MEDICATIONS
Stop guessing with neurological medications. This DNA test reveals how your body responds to treatments for epilepsy, cognitive decline, migraines, and more—for safer, smarter prescribing.
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PGx testing reveals how your genes influence your response to neurological medications - from antiepileptics to memory aids - supporting safer and more effective care.
Tailor drugs like phenytoin, donepezil, or clobazam to your DNA.
Lower risk of sedation, dizziness, or poor function.
Manage seizures, movement, or cognitive symptoms more precisely.
Confidence your treatment aligns with your biology.
Avoid delays caused by trial-and-error medication cycles.
The customer service is great. The team are very responsive and proactive with their customers. They always return calls if not immediately available. They listen to questions, desired options and work hard to apply good suggestions.
Their products and services are good and very helpful for my clinical practice.
I ordered the cardiovascular test as I had refused statins based on friends suffering side effects and wanted to assess whether I was statin intolerant. The stated turnaround time of up to 14 days was well met with a result within 6 days of taking the sample.
The test report, which is exceptionally well presented and clear, showed that had I gone blindly to the GP the NICE guideline 1st and 2nd line statin choices would have resulted in moderate side effects. I can now approach the GP with an informed choice that will hopefully result in reduced cholesterol.
Fast turnaround
Sensible pricing
Good communication
Excellent
I recently used AttoDiagnostics for pharmacogenomic testing and was really impressed with the entire experience. The recommendations were clear and practical, and I was able to forward the report to my doctor, who also found it very useful for ongoing treatment decisions. It’s rare to receive this level of depth and clarity in such a specialised area of healthcare. Highly recommend Atto Diagnostics to anyone looking for accurate genetic testing with thorough analysis and human-centred support.
Complimentary Experience
I used AttoDiagnostics for pharmacogenomic (PGx) testing and was impressed from start to finish. Communication was excellent; proactive updates, quick responses, and clear next steps at every stage. The results were easy to understand, with practical guidance that helped me have a more informed conversation with my clinician. No jargon, no pressure, just transparent, professional service. If you’re considering PGx testing to optimize medications, I highly recommend AttoDiagnostics for their clarity and customer care.
Great service. Fast delivery, results processed quickly and insights very helpful.
Great test, and really gave me peace of mind on what drugs I would be better suited to in the future. Purchased after a family health scare.
Very impressed by the speed of test results and the number of drugs listed that potentially may affect me. Relieved that non were likely to affect me which was reassuring but interestingly varying the dosage of some may be beneficial for me.
Complimentary Experience
Great service - quick delivery and turnaround of results. Report is very comprehensive and straightforward to interpret. Support team responsive and very helpful.
This test breaks drugs down into a 1, 2 or 3, based on your genetic profile. 1’s are great. Drugs in the 2 family need additional considerations. Avoid 3’s. Take this report?with you whenever you go to see your GP.
Complimentary Experience
Understand how your body metabolises neurological medications — including anticonvulsants, beta blockers, and cognitive enhancers — based on your unique genetic make-up.
See which neurology medications are most likely to work for you, based on your genes — reducing the risk of side effects and improving treatment success.
This section offers a detailed overview of neurological medications. Each is categorised as follows:
- Mild or no known gene-drug interaction: Safe to use as recommended.
- Moderate gene-drug interaction: May require dose adjustment or monitoring to avoid side effects.
- Severe gene-drug interaction: Increased risk of poor response or adverse effects — consider alternative medications suited to your genetic profile.
In-depth analysis of how your body processes neurological medications, supported by peer-reviewed science and clinical guidelines.
Pharmacogenomics (PGx) reveals how your genes affect your response to neurological medications like anticonvulsants, cognitive enhancers, and migraine preventatives. We make it simple.
Step 1
A quick cheek swab — painless and easy. Includes clear instructions and a pre-paid return envelope.
Step 2
Your sample is processed at our accredited UK lab. We analyse 120+ genetic markers to understand how your body processes key neurology drugs.
Step 3
Your tailored report helps you and your clinician choose the right medications - improving outcomes and reducing risks for conditions like epilepsy, Parkinson’s, migraines, and memory loss.
By taking the test, you provide your healthcare professional with an essential tool to ensure that your prescriptions are tailored to your unique genetics. As a result, your road to recovery can be shorter and more effective.
IMPORTANT: DO NOT MAKE ANY CHANGES TO YOUR CURRENT MEDICATION(S) WITHOUT CONSULTING YOUR HEALTHCARE PROVIDER FIRST.
While your genetics is important, other factors also contribute to how you respond to medications. The final choice of medication used will be based on your healthcare provider’s professional judgement and may be different to what is recommended in this report. The AttoPGx test does not determine your risk of any health problem or condition. It only evaluates select portions of your DNA that help predict how you may respond to the medications covered.
What is PGx testing for neurology?
Pharmacogenomic (PGx) testing analyses your DNA to understand how your body responds to certain medications. It helps healthcare professionals tailor treatments to your unique genetic profile, ensuring medications are effective and minimising side effects.
Who can benefit from PGx testing?
This test is particularly helpful for individuals who:
What medications are covered in the test?
The test includes insights into key neurological medications such as anti-epileptics, dopaminergic medications, pain management drugs, and more.
How does the test work?
Where is the test performed?
The test is processed in a UK laboratory using advanced platforms including ThermoFisher OpenArray technology and/or Illumina iScan system, ensuring precise results.
Is the test painful?
No, the test is completely non-invasive. It involves a simple cheek swab that you can complete at home in just a few minutes.
How accurate is PGx testing?
Our testing process uses state-of-the-art technology and analyses over 120 genetic markers to provide precise, clinically actionable insights. However, genetics is just one factor influencing medication response, and results should be used in consultation with a healthcare provider.
Do I need a doctor to interpret my PGx results?
While the report is designed to be user-friendly, we strongly recommend discussing your results with your healthcare provider. They can interpret the findings in the context of your overall health and treatment plan.
How does PGx testing help reduce side effects?
By analysing your genetic profile, PGx testing identifies medications that are more likely to work for you and those that might cause adverse reactions. This helps your healthcare provider to make more informed decisions, minimising the risk of side effects.
What happens if my genetic profile suggests my current medication isn’t suitable?
Your healthcare provider may use the report to adjust your treatment plan, such as changing the medication or dosage, to find a more effective and safer option.
Can I change my medications based on the report?
No. You should never adjust your medications without consulting your healthcare provider. The PGx test provides guidance for your healthcare practitioner, who will make the final treatment decisions.