Conexiant
Login
  • The Analytical Scientist
  • The Cannabis Scientist
  • The Medicine Maker
  • The Ophthalmologist
  • The Pathologist
  • The Traditional Scientist
The Pathologist
  • Explore Pathology

    Explore

    • Latest
    • Insights
    • Case Studies
    • Opinion & Personal Narratives
    • Research & Innovations
    • Product Profiles

    Featured Topics

    • Molecular Pathology
    • Infectious Disease
    • Digital Pathology

    Issues

    • Latest Issue
    • Archive
  • Subspecialties
    • Oncology
    • Histology
    • Cytology
    • Hematology
    • Endocrinology
    • Neurology
    • Microbiology & Immunology
    • Forensics
    • Pathologists' Assistants
  • Training & Education

    Career Development

    • Professional Development
    • Career Pathways
    • Workforce Trends

    Educational Resources

    • Guidelines & Recommendations
    • App Notes

    Events

    • Webinars
    • Live Events
  • Events
    • Live Events
    • Webinars
  • Profiles & Community

    People & Profiles

    • Power List
    • Voices in the Community
    • Authors & Contributors
  • Multimedia
    • Video
    • Podcasts
Subscribe
Subscribe

False

The Pathologist / Issues / 2025 / Apr / Pharmacogenomics and Adverse Drug Reactions
Omics Genetics and epigenetics Molecular Pathology Precision medicine Screening and monitoring

Pharmacogenomics and Adverse Drug Reactions

Genetic testing could prevent thousands of serious drug side effects, UK study finds

04/02/2025 News 2 min read

Share

A new analysis of six decades of adverse drug reaction (ADR) reports in the UK has revealed that up to 1 in 11 medication side effects could potentially be avoided by tailoring prescriptions to a patient’s genetic makeup. The findings, published in PLOS Medicine, highlight the value of pharmacogenomic testing and point to psychiatry as a key area for implementation.

Researchers from Queen Mary University of London examined more than 1.3 million ADRs reported through the UK's Yellow Card scheme, identifying over 115,000 (9 percent) linked to drugs known to interact with specific genetic variants. These are medications for which guidelines already exist recommending altered prescribing based on a patient’s genetic profile.

Notably, just three genes – CYP2C19, CYP2D6, and SLCO1B1 – accounted for 75 percent of the gene-associated reactions. These genes influence how the body processes drugs, including many commonly used psychiatric, cardiovascular, and pain medications.

Psychiatric medications alone accounted for nearly half (47 percent) of all potentially preventable ADRs. While most reactions were severe but non-fatal, some – such as cardiac arrhythmias – were fatal, although rare. Older patients were more likely to experience genetically linked ADRs, and these were more often reported by patients and carers than by industry. The study also found that psychiatric drugs were overrepresented in ADR reports compared with how often they are prescribed, suggesting a greater opportunity to improve safety through personalized prescribing.

The authors estimate that around 30 percent of these ADRs could have been avoided with the use of a pre-emptive genetic test, as shown in the European PREPARE trial. Coauthor Mark Caulfied said, “It is time for the National Health Service to consider adopting pre-emptive testing for known genes that interact with medications.”

The researchers argue that even a limited gene panel could have a major impact and help reduce healthcare costs, hospitalizations, and patient harm – particularly in psychiatry, where the need appears greatest.

As prescribing becomes more complex and polypharmacy increases with aging populations, the authors call for pilot programs to test real-world implementation of pharmacogenomics in UK healthcare. 

Newsletters

Receive the latest pathology news, personalities, education, and career development – weekly to your inbox.

Newsletter Signup Image

Explore More in Pathology

Dive deeper into the world of pathology. Explore the latest articles, case studies, expert insights, and groundbreaking research.

False

Advertisement

Recommended

False

Related Content

Turning Tides
Omics
Turning Tides

January 9, 2024

3 min read

A new study shows evidence for sustained human-to-human transmission of mpox since 2016

“Pop” Goes the Sensor
Omics
“Pop” Goes the Sensor

January 19, 2022

1 min read

A new device could help scientists identify signs of arrhythmia, heart attack, and cardiac fibrosis

Improving Risk Stratification
Omics
Improving Risk Stratification

February 3, 2022

1 min read

Two genes have been identified that may be linked to prostate cancer outcomes

The Ultimate Vision for Rare Disease
Omics
The Ultimate Vision for Rare Disease

February 28, 2022

1 min read

Genomics and computational pathology can take rare disease diagnostics to the next level

False

The Pathologist
Subscribe

About

  • About Us
  • Work at Conexiant Europe
  • Terms and Conditions
  • Privacy Policy
  • Advertise With Us
  • Contact Us

Copyright © 2025 Texere Publishing Limited (trading as Conexiant), with registered number 08113419 whose registered office is at Booths No. 1, Booths Park, Chelford Road, Knutsford, England, WA16 8GS.