A pharmacogenetics test analyses specific genes involved in how your body processes medications. The results can help predict whether certain medicines may work normally, less effectively, or cause an increased risk of side effects.

Your genes influence how quickly your body breaks down and processes medicines. Some people metabolise medications very quickly, while others process them more slowly, which can affect effectiveness, dosing, and the likelihood of side effects.

This test may be helpful for people who:

• Experience side effects from medication
  
• Feel their medication is not working as expected
  
• Use multiple medications
  
• Want proactive insight before starting treatment
  
• Have a history of unusual medication responses
  

It can also be valuable for doctors and pharmacists when choosing medication or adjusting dosage.

The test does not directly prescribe medication, but it can provide valuable information about how your body may respond to certain medicines. Your doctor or pharmacist can use this information to support treatment decisions.

No. The test analyses your DNA, which does not change based on current medication use. You can usually continue taking your medication as prescribed unless advised otherwise by your healthcare provider.

No. Your pharmacogenetic profile is lifelong and does not change over time. In most cases, this test only needs to be performed once.

Yes. The report is designed to be shared with healthcare professionals and may help support medication reviews, dosing decisions, and treatment discussions. Some pharmacies can also register pharmacogenetic results in your medication file.

No. A genetic variant does not automatically mean a medication is dangerous or unsuitable. In many cases, the information may simply help guide dosage adjustments or closer monitoring.

Yes. Many people choose pharmacogenetic testing proactively so they already have their genetic medication profile available if they need medication in the future.