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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.

Please see information below to report adverse events in the UK

Adverse events should be reported. Reporting forms and information can be found at: www.mhra.gov.uk/yellowcard.
Adverse events should also be reported to Proveca Limited.
Phone: 0333 200 1866 E-mail: medinfo@proveca.com

Please see information below to report adverse events in the Republic of Ireland

Adverse events should be reported. Reporting forms and information can be found at: www.hpra.ie.
Adverse events should also be reported to Proveca Limited.
Phone: +44 333 200 1866 E-mail: medinfo@proveca.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 about adverse event reporting can be found at:

Flag of the United KingdomUnited Kingdom

www.mhra.gov.uk/yellowcard.

Flag of IrelandIreland

HPRA – Pharmacovigilance: Earlsfort Terrace, IRL – Dublin 2

Tel: +353 1 6764971
Fax: +353 1 6762517
Website: www.hpra.ie
e-mail: medsafety@hpra.ie

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: medinfo@proveca.com

UK-NON-23-0020
Reviewed June 2023