HOW TO REPORT A PROBLEM WITH SIALANAR®
Proveca Ltd routinely monitors the safety of its medicines. This includes review of safety data from clinical studies and collection of reports and cases of adverse events for marketed products. The information contributes to the continuing safety surveillance of our products.
If you become aware of a patient who has experienced an adverse event, pregnancy, overdose or unexpected benefits with one of our products, we would be grateful if you would contact Proveca Ltd Medical Information on +44 0333 2001866 or email: email@example.com
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. More information can be found at:
HPRA – Pharmacovigilance: Earlsfort Terrace, IRL – Dublin 2
Tel: +353 1 6764971: Fax: +353 1 6762517: Website: www.hpra.ie: e-mail: firstname.lastname@example.org
If you have a problem with the quality of Sialanar® please contact Proveca Ltd Medical Information on +44 0333 2001866 or email: email@example.com
Created April 2020