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: email@example.com
More information about adverse event reporting can be found at www.mhra.gov.uk/yellowcard.
If you have a problem with the quality of Sialanar® or its packaging please contact Proveca Ltd Medical Information on +44 (0)333 2001866 or email: firstname.lastname@example.org
Created March 2020