Adverse events should be reported to your local regulatory authority and Allergan office.
Adverse Event (AE): Any untoward medical occurrence in a patient administered an Allergan marketed product and which does not necessarily have to have a causal relationship with this treatment. An adverse event can be any unfavorable and unintended sign (including an abnormal laboratory finding, for example), symptom, or disease temporally associated with the use of an Allergan product, whether or not considered related to the Allergan product.
Allergan Pharmaceuticals (VISTABEL®)
Phone: +44. (0)1628 494456
When contacting us please include: product name; dose; anonymised patient details; information about the event and the reporter contact details. You may be contacted to provide further details.
Allergan Medical Devices (FILLERS and IMPLANTS)
Please follow this link to report an adverse event related to Allergan Medical Devices.
Once on the page you can use the drop down menu on the top right corner to select a different language.