THIS SITE IS INTENDED FOR UK AND IRELAND HEALTH PROFESSIONALS ONLY
CREATED BY LEO PHARMA

Report an adverse event

Reporting of Suspected Adverse Events

Adverse events should be reported.

UK reporting adverse events:

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

Adverse events should also be reported to Drug Safety at LEO Pharma.
Tel: +44 (0)1844 347333
e-mail: medical-info.uk@leo-pharma.com

IE reporting adverse events:

Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via HPRA Pharmacovigilance, Earlsfort Terrace, Dublin 2,
Tel: +353 1 6764971
Fax: +353 1 6762517
Website: www.hpra.ie
e-mail: medsafety@hpra.ie

Adverse events should also be reported to Drug Safety at LEO Pharma
Tel: +353 1 4908924
e-mail: medical-info.ie@leo-pharma.com