How to report a problem with Proveca medicines
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.
Please see information below to report adverse events in the UK
Please see information below to report adverse events in the Republic of Ireland
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 about adverse event reporting can be found at:
If you have a problem with the quality of a Proveca medicine or its packaging please contact Proveca Ltd Medical Information on +44 (0)333 2001866 or email: firstname.lastname@example.org
Reviewed June 2023