FAQ

Q&A:

1. What is pharmacogenomics?

Pharmacogenomics is the study of how a person's genetic makeup affects their response to medications.

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2. How does pharmacogenomics work?

Pharmacogenomics works by analyzing a person's DNA to identify genetic variants that may affect their response to medications. By understanding a person's genetic makeup, healthcare providers can better predict which medications will be most effective and have the fewest side effects for that individual.

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3. What are the benefits of pharmacogenomics testing?

The benefits of pharmacogenomics testing include a more personalized approach to medication therapy, improved medication effectiveness, reduced medication costs, and a reduced risk of adverse drug reactions.

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4. Who can benefit from pharmacogenomics testing?

Anyone can benefit from pharmacogenomics testing, but it may be particularly helpful for individuals with a history of adverse drug reactions, those who require multiple medications, or those who have not responded well to previous medication therapies.

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5. What type of sample is needed for pharmacogenomics testing?

A sample for pharmacogenomics testing typically involves a swab of the inside of the cheek or a blood sample.

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6. Are pharmacogenomics tests covered by insurance?

Some insurance plans may cover the cost of pharmacogenomics testing, but coverage can vary depending on the specific plan and the reason for the testing.

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7. How do I interpret my pharmacogenomics test results?

Interpreting pharmacogenomics test results can be complex and may require the assistance of a healthcare provider or genetic counselor. We offer a free one-to-one test interpretation to every customer tested with us.

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8. What should I do with my pharmacogenomics test results?

Individuals should discuss their pharmacogenomics test results with a healthcare provider to determine how to best use the information to guide medication therapy. In some cases, changes to medication dosages or drug selection may be recommended based on the results.