Medical Information Enquiries
For all product and medical information queries or to report adverse events or product complaints please contact:
Actavis UK Limited
Adverse events* should be reported. Reporting forms and information can also be found at http://www.mhra.gov.uk/yellowcard
Adverse events should also be reported to Actavis on 01271 385257.
* Patient safety is Actavis UK Limited primary concern and we encourage healthcare professionals and members of the public to report any adverse event which may occur in relation to an Actavis UK Limited product. An adverse event includes reports of any side effect, product misuse, abuse or overdose, including inappropriate use by children or women who are pregnant or breast-feeding. It also includes reports of a product that was used for something other than the intended purpose or was ineffective, or was given with another medicine. Complaints relating to the product can also be reported.
For general enquiries please contact: