Report a problem

How to report a problem with Proveca medicines

Side effects

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, lack of effect or unexpected benefits with one of our products, we would be grateful if you would contact Proveca Ltd Medical Information on +44 (0)333 2001866 or email:

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:

Flag of IrelandIreland

HPRA – Pharmacovigilance: Earlsfort Terrace, IRL – Dublin 2

Tel: +353 1 6764971
Fax: +353 1 6762517

Product quality

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:


Reviewed November 2021