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Featuring
PRECISE Pharmacogenomics
Unlock the power of genome-wide technology to personalize your medication like never before. With PRECISE Pharmacogenomics, discover how your genetic makeup influences your response to medications.
As a pre-emptive pharmacogenomics test, it provides clinically backed recommendations, empowering healthcare providers to prescribe safer, more effective treatments tailored just for you.
- Covers 1,000+ genes & 500+ commonly prescribed medications
- Supports 20+ therapeutic areas, including oncology (cancer), cardiology (heart health), neurology (brain health), pain management & more
- Clinically accredited & recommended for precision treatment
- Maximizes and optimizes medication effectiveness
What Is Pharmacogenomics (PGx)?
Pharmacogenomics, otherwise abbreviated as PGx, is the study of how your genes influence your response to medication. Just as everyone’s DNA is unique, so is the way we process medications or drugs.
By analyzing your genetic makeup, PGx helps predict which medications will be most effective, which may cause side effects, and what dosages suit you best — reducing trial and error for safer, more personalized treatments.
What's the difference?
Pre-emptive vs. Reactive Pharmacogenomics
| CHARACTERISTICS | PRE-EMPTIVE PHARMACOGENOMICS | REACTIVE PHARMACOGENOMICS |
|---|---|---|
|
TIMING |
Done before prescribing medication. |
Done after an adverse reaction or treatment failure. |
|
APPROACH |
PROACTIVE – helps doctors select the safest, most effective medication upfront, reducing side effects. |
REACTIVE – testing is only done in response to medication issues. |
|
EXAMPLE |
A patient scheduled for long-term medication (e.g., for high blood pressure) undergoes testing to ensure the best drug choice. |
A patient suffers severe side effects from a painkiller. Testing later reveals poor drug metabolism, prompting a prescription change. |
|
BENEFIT /LIMITATION |
BENEFIT: Reduces trial and error, enhances treatment success. |
LIMITATION: The patient experiences adverse (negative) effects before adjustments are made. |
Why Pharmacogenomics?
Unlocking Safer, More Effective Medications With Pharmacogenomics
Adverse drug reactions remain a major global concern, but pharmacogenomics offers a groundbreaking solution. By understanding how your genes influence drug response, we can reduce trial-and-error prescribing and improve treatment outcomes. Here’s why pharmacogenomics testing matters;
- Adverse Drug Reactions (ADRs) are the 6ᵗʰ leading cause of death worldwide ¹ ².
- 99.5% of individuals have at least 1 gene variant that affects drug response, requiring dosage adjustments ⁸.
- Pharmacogenomics accounts for ~80% of gene variability linked to drug safety and effectiveness ³.
- The FDA has issued pharmacogenomic-related warnings for drugs like Codeine Sulfate, Clopidogrel and Rasburicase ⁴ ⁵.
- About 70% of physicians adjust medications or dosages using pharmacogenomics testing to reduce ADRs ⁶.
- Pharmacogenomics testing has been proven to significantly reduce ADRs and medication side effects ⁷.
How does it benefit me?
Benefits Of Pharmacogenomics (PGx):
Enhancing Treatment Precision
By using pharmacogenomics, you can get safer, more effective, and cost-efficient treatments that are tailored to your unique genetic makeup.
7.6% Improvement
in medication adherence when PGx testing guides treatment ².
Cost savings on medication
by avoiding ineffective treatments and unnecessary prescriptions ³ ⁴.
Reduced trial-and-error prescribing
benefiting healthcare providers and mental health therapies ⁵.
How does it work?
How Pharmacogenomics Works
Your body processes medications through Absorption, Distribution, Metabolism, and Excretion (ADME). These steps determine how well a drug works and whether you might experience side effects.
Pharmacogenomics analyzes your DNA to see how fast or slow your body breaks down medications. Based on your genes, you may be;
Poor
Metabolizer
Your body processes the drug too slowly, increasing the risk of side effects.
Intermediate
Metabolizer
You process drugs slightly slower, so adjustments may be needed.
Normal
Metabolizer
You break down drugs at the expected rate, so standard doses usually work well.
Rapid or Ultra-Rapid Metabolizer
Your body breaks down the drug too quickly, making it less effective.
Knowing your metabolizer type helps doctors choose the right medication and dosage for you, reducing side effects and guesswork.
Why Choose PRECISE Pharmacogenomics?
⚠️ Only Clinically Accredited DNA test can be used by healthcare professionals to make important treatment decisions.
PRECISE PHARMACOGENOMICS (PGx)
Book An Appointment Today!
Personalize your medication, minimize side effects, and optimize treatment with
PRECISE Pharmacogenomics.
Real Stories, Real Impact
How PRECISE Pharmacogenomics Is Changing Lives
Click any of the following to find out more about how PRECISE Pharmacogenomics is making a difference.
Note: Please click on this image to view the case study details.
How to start?
How To Get Started With Your PRECISE Pharmacogenomics Test
Contact Precision Diagnostics or visit your nearest PRECISE Pharmacogenomics panel to obtain your test
Choose the collection method between a buccal swab (self-administered) or a blood draw (requires an appointment) at a designated facility.
Your sample is sent to the Precision Diagnostics' laboratory for processing.
Your results will be ready in 4 to 6 weeks. You'll receive an email and SMS notification once your report is available in our app, PreciseEHR.
Book your complimentary one-on-one consultation with a healthcare professional to review your results.
Get Your Test Kit
Contact Precision Diagnostics or visit your nearest PRECISE Pharmacogenomics panel to obtain your test.
Collect Your Sample
Choose the collection method between a buccal swab (self-administered) or a blood draw (requires an appointment) at a designated facility.
Lab Analysis
Your sample is sent to the Precision Diagnostics’ laboratory for processing.
Receive Your Report
Your results will be ready in 4 to 6 weeks. You’ll receive an email and SMS notification once your report is available in our app, PreciseEHR.
Consult with an Expert
Book your complimentary one-on-one consultation with a healthcare professional to review your results.
available now
Go Paperless With PreciseEHR
Take charge of your health with PreciseEHR, your secure electronic health record (EHR) platform. Access your Pharmacogenomics report, track your health data, and stay informed—all in one place.
- Comprehensive Reports — Get detailed, easy-to-interpret insights at your fingertips.
- Intuitive Interface — Navigate effortlessly for a smooth experience.
- Secure & Compliant — Keep your data protected with top-tier security.
- Real-time Updates — Stay informed with instant access to the latest reports.
- Easy Access — View your reports anytime, anywhere and accessible
one-to-one personalized consultation
PRECISE Pharmacogenomics
Doctor Panel
Get a personalized one-to-one consultation with our expert doctors to help you understand your pharmacogenomic report
Dr. Nada Syazana Zulkufli
MBBS (Monash), MRCPI (Ireland), MPATH (Chemical)(UM), AM (Mal)
Assoc. Prof. Dr. Hoo Fan Kee
MD (Mal), MRCP (UK), MRCPS (Glasgow)
Frequently Asked Questions
What is the difference between DNA testing and Pharmacogenomics?
DNA testing, or genetic testing, comes in many forms, including tests for ancestry, relationships, inherited diseases, cancer risks, and medical diagnoses. These tests analyze your genes, chromosomes, or proteins to detect genetic conditions, assess disease risk, or determine hereditary traits.
Pharmacogenomics (PGx), on the other hand, focuses specifically on how your genes affect your response to medications. It helps healthcare professionals personalize treatment plans, reduce the risk of adverse drug reactions (ADRs), optimize drug selection and dosage.
While genetic testing can help identify potential health risks, PRECISE Pharmacogenomics (PGx) ensures that your medications are tailored specifically for you—enhancing safety and treatment effectiveness.
Is PRECISE Pharmacogenomics reliable?
Yes. PRECISE Pharmacogenomics (PGx) provides comprehensive genome-wide coverage, analyzing nearly 100,000 ADME markers and over 1,000 genes, covering more than 500 commonly used medications, including:
- Painkillers
- Antibiotics
- Diabetes medications
- Heart disease treatments
- Cancer therapies
Awarded as “The First Clinical Recommended Genome-Wide Pharmacogenomics” by the Malaysia Book of Records, this DNA report is user-friendly. Only certified healthcare professionals are qualified to interpret the report to provide clinical recommendations, diagnoses, and treatment plans. Please note that this report does not replace a medical consultation with your doctor.
How accurate is PRECISE Pharmacogenomics?
PRECISE Pharmacogenomics (PGx) boasts an analytical accuracy of over 99%, making it one of the most precise and reliable pharmacogenomics test available. Our platform is backed by PRECISE Pharmacogenomics (PGx) boasts an analytical accuracy of over 99%, making it one of the most precise and reliable pharmacogenomics test available. Our platform is backed by CAP & ISO 15189 laboratory compliance for high accuracy and quality. standards.
Who should consider getting a PRECISE Pharmacogenomics test?
PRECISE Pharmacogenomics test is beneficial for both people who are currently taking medications (reactive testing) and those who want to be proactive and prepare before starting new medications (pre-emptive testing). It’s designed to find the right medication at the right dose for you. This test is especially recommended for:
- Individuals on long-term medications (e.g., hypertension, diabetes, mental health conditions).
- People taking multiple medications (e.g., for chronic or complex health issues).
- Those with a history of medications side effects and/or found treatment ineffective.
- Individuals who want to ensure their medications are both safe and effective.
- Anyone who is proactive and have their genetic-drugs information ready to guide future prescriptions, so doctors can choose the right medication from the start, even in emergencies, acting as “genomic insurance.”
Can children or elderly individuals take the PRECISE Pharmacogenomics test?
Yes! PRECISE Pharmacogenomics testing is suitable for all ages and can be especially beneficial for:
• Children – Helps identify potential drug responses early, ensuring safer and more effective treatments as they grow.
• Elderly individuals – Particularly useful in managing multiple medications, reducing the risk of medication side effects and ensuring medications are tailored for safer use.
Because your genetic blueprint remains the same for life, the PRECISE Pharmacogenomics test is a once-in-your-lifetime test that provides lifelong value. Your DNA results can guide safe and effective medication choices for the rest of your life.
Does my pharmacogenomics result change over time?
No. Your genetic blueprint does not change over time, meaning your pharmacogenomics results remain valid for life. However, as new medications and research emerge, updates may be available to enhance treatment recommendations.
PRECISE PHARMACOGENOMICS (PGx)
Book An Appointment Today!
Personalize your medication, minimize side effects, and optimize treatment with
PRECISE Pharmacogenomics.
References:
- Oster H, Chaves I. Effects of Healthy Lifestyles on Chronic Diseases: Diet, Sleep and Exercise. Nutrients. 2023 Oct 31;15(21):4627. doi: 10.3390/nu15214627. PMID: 37960280; PMCID: PMC10650398.
- Shang, X., Liu, J., Zhu, Z. et al.Healthy dietary patterns and the risk of individual chronic diseases in community-dwelling adults. Nat Commun 14, 6704 (2023). https://doi.org/10.1038/s41467-023-42523-9
- Bösch ES, Spörri J, Scherr J. Vitamin Metabolism and Its Dependency on Genetic Variations Among Healthy Adults: A Systematic Review for Precision Nutrition Strategies. Nutrients. 2025 Jan 10;17(2):242. doi: 10.3390/nu17020242. PMID: 39861372; PMCID: PMC11767394.
- Madeo G, Donato K, Micheletti C, Cristoni S, Miertus S, Miertus J, Veselenyiova D, Iaconelli A, Aquilanti B, Matera G, Connelly ST, Bertelli M. Nutrigenomics: SNPs Correlated to Lipid and Carbohydrate Metabolism. Clin Ter. 2023 Nov-Dec;174(Suppl 2(6)):200-208. doi: 10.7417/CT.2023.2488. PMID: 37994765.
- Laddu D, Hauser M. Addressing the Nutritional Phenotype Through Personalized Nutrition for Chronic Disease Prevention and Management. Prog Cardiovasc Dis. 2019 Jan-Feb;62(1):9-14. doi: 10.1016/j.pcad.2018.12.004. Epub 2018 Dec 13. PMID: 30553801.
- Karvela, M., Golden, C.T., Bell, N. et al.Assessment of the impact of a personalised nutrition intervention in impaired glucose regulation over 26 weeks: a randomised controlled trial. Sci Rep 14, 5428 (2024). https://doi.org/10.1038/s41598-024-55105-6