Welcome

Please select one of the following links below to access information relevant to you

  • Great Britain Healthcare Professional

    Reporting adverse events and quality complaints

    This medicine is subject to additional monitoring. This will allow quick identification of new safety information. 

    Adverse events should be reported.

    Reporting forms and information can be found at https://yellowcard.mhra.gov.uk/

    Adverse events should also be reported to Bayer plc.

    If you want to report an adverse event or quality complaint, reports can be directed to: Tel: 01182063500 or Email: pvuk@bayer.com

    Further information is available on the "contact" tab at www.bayer.co.uk.

  • Patients who have been prescribed Kerendia▼(finerenone)

    Report possible side effects

    This medicine is subject to additional monitoring. This will allow quick identification of new safety information. 

    If you get any side effects, talk to your doctor, pharmacist or nurse. 

    This includes any possible side effects not listed in the package leaflet. You can also report side effects directly via the Yellow Card Scheme at https://yellowcard.mhra.gov.uk/ or search for MHRA Yellow Card in Google Play or Apple App Store. 

    You can also report side effects and quality complaints to Bayer plc. 

    Further information is available on the "contact" tab at www.bayer.co.uk.

    By reporting side effects you can help provide more information on the safety of this medicine.

This site has been produced and funded by Bayer

RP-KER-GB-0440 | September 2023