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PP-VER-GB-0036 | November 2022

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 www.mhra.gov.uk/yellowcard. 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: 0118 206 3500 or Email: pvuk@bayer.com

 

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

 

 

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  • Which patients are
    suitable for Verquvo?
  • How does Verquvo
    work?
  • How is Verquvo
    prescribed?
  • Verquvo
    data
  • Resources
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  • Conditions of Use
  • Imprint
  • Report a Side Effect
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  • Sitemap
  • Contact us
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  • Home
  • Which patients are
    suitable for Verquvo?
  • How does Verquvo
    work?
  • How is Verquvo
    prescribed?
  • Verquvo
    data
  • Resources
  • Privacy policy
  • Conditions of Use
  • Imprint
  • Report a Side Effect
  • Full Prescribing Information
  • Cookie Settings
  • Sitemap
  • Contact us

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This website contains information on Verquvo® (vericiguat) which is based on the Summary of Product Characteristics (SmPC). Intended for UK audience only.

  • PP-VER-GB-0028 November 2022
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