Medicine safety

We are committed to the safety of our medicines in all cases, and maintain an active pharmacovigilance programme to help ensure this.

Through our robust commitment to pharmacovigilance, we ensure we remain focused on patients' safety. Our Pharmacovigilance Department manages a pharmacovigilance system for the collection, collation, and evaluation of adverse events and the implementation of effective corrective and preventive actions.

 

EU Medical Information Enquiries, Complaints and Adverse Events Reporting

For further information or to report adverse events in EU, please contact portugaleupharmacovigilance@hikma.com 

 

US Medical Information Enquiries, Complaints and Adverse Events Reporting

For further information or to report adverse events in the US, please contact us.hikma@primevigilance.com or call +1-877-845-0689 or 1-800-962-8364, or you can contact the FDA directly at 1-800-FDA-1088 or www.fda.gov/medwatch.

          

Rest of the World Medical Information Enquiries, Complaints and Adverse Events Reporting

For all other enquires or to report events which occurred outside the EU or the US please contact pharmacovigilance@hikma.com