The Mantara pharmacogenomics (PGx) DNA test helps personalise prescribing by looking at how your genes affect the way your body responds to medicines. Everyone processes medications differently, and much of this variation is driven by genetics. This test is designed to help your clinician choose the right medication and dose for you, reducing the risk of side effects and improving how well treatments work.
The test is simple and non-invasive. You provide a small saliva sample at home using an easy collection kit, which is then sent to the laboratory for analysis. Your DNA is examined for genetic variants known to influence how the body metabolises and responds to many commonly prescribed medicines. You receive a clear, personalised report that can be shared with your GP or specialist to guide current and future prescribing decisions.
The Mantara PGx test is a one-time test with long-term value, as your genetic information does not change. It covers over 70 commonly prescribed medications, including treatments for heart health, mental health, pain relief and blood thinning. The results are based on well-established clinical research and recognised pharmacogenomic guidelines, helping clinicians tailor treatment more precisely to you.
Many people experience unwanted side effects or limited benefit from medications because standard prescribing does not account for individual genetic differences. Pharmacogenomics helps explain why this happens and provides an evidence-based way to move away from trial-and-error prescribing. The Mantara PGx DNA test supports safer, more personalised care by giving you and your clinician better information from the outset, helping treatments work more effectively with fewer side effects.
PRODUCT INFO
Once in a lifetime test to personalise your medication
RETURN & REFUND POLICY
Non-refundable