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Adverse Events

Adverse Events

UK: Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard. Adverse events should be reported to Women’s Health Division of Gedeon Richter (UK) Ltd on 0207 604 8806 or drugsafety.uk@gedeonrichter.eu

ROI: Adverse events should be reported to the HPRA Pharmacovigilance, Earlsfort Terrace, IRL – Dublin 2, Tel: +353 16764971, Website: www.hpra.ie, email: medsafety@hpra.ie. Adverse events should be reported to Women’s Health Division of Gedeon Richter (UK) Ltd on +44 207 604 8806 or drugsafety.uk@gedeonrichter.eu