Reporting adverse events
Adverse event and product complaint reports
Adverse event and product complaint reports
Adverse Events and any drug or medical device product quality complaints (including suspected defective medicines or medical device adverse incidents) should be reported. For the UK reporting forms and information can be found at www.mhra.gov.uk/yellowcard. For Ireland report to the Health Products Regulatory Authority (HPRA) using a Yellow Card obtained from the HPRA, via the online system (www.hpra.ie) or by telephone on +353 (0)1-6764971.
Pharmacovigilance Adverse Event reporting
If you have a drug safety concern or would like to report an adverse event.
Phone: 01635 206360
Email: [email protected]
For further information in relation to pharmacovigilance and adverse event reporting visit baxterhealthcare.co.uk/pharmacovigilance
Read the Pharmacovigilance Privacy Statement
Quality
Baxter’s Quality Team is responsible for reporting and monitoring all product related complaints and concerns.
Phone: 01635 704603
Email: [email protected]
For queries regarding Field Corrective Actions (safety corrections and product recalls):
Email: [email protected]
Other quality queries: [email protected]