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This website is intended for UK and IRE healthcare professionals only

Adverse Event Reporting

For the United Kingdom:
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 Kyowa Kirin International UK NewCo Ltd, known as Grünenthal Meds on +44 (0)1896 664000, email PVUK@grunenthalmeds.com

For the Republic of Ireland:
Adverse Events should be reported.
Information about adverse event reporting can be found at www.hpra.ie.

Adverse Events should also be reported to Kyowa Kirin International UK NewCo Ltd, known as Grünenthal Meds on +44 (0)1896 664000, email PVUK@grunenthalmeds.com