Genetic testing for

Pharmacogenetics

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Pharmacogenetics

According to official data from the European Union, it is estimated that 5% of people admitted to A&E as a cause of adverse reaction to medication, causing 197.000 deaths annually.

Studying the genetic variability of an individual in response to certain medication is vital in order to determine which medication and which dosage should be prescribed in order to avoid adverse reactions or therapeutic failure. In this way, health professionals are able to prescribe medication in a secure and efficient way, avoiding therapeutic failure, minimising adverse reactions to medication and significantly reducing the cost to medical assistance.

At Reference Laboratory Genetics we have a wide range of tests specialised in pharmacogenetics, enabling us to offer the most appropriate test to each patient: from screening to diagnosis, including prevention and prognosis. What’s more we also offer therapeutic monitoring of medication to help individualise the therapy of each patient.

Our specialised pharmacogenetic tests include genes related with the metabolism of various medication:

Continually updated panels using HPO in order to include the most recent association published between phenotype and genotype.

Lower number of VOUS thanks to our database Reflab Database®, and main genetic variants and specific to illness databases.

The best turnaround times (< 30 days).

Pre and postanalysis support with our experts in clinical genetics.

Conclusive, transparent and customizable clinical reports.

Maximum diagnostic yield and clinical utility.

Download information

NGS Diagnostic Catalogue
Pharmacogenetics
NGS Diagnostic Catalogue

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    We have optimized all our processes to accept a wide range of samples, always adapting to each case.

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