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.

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.

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.

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.”

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.

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.