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.
Adverse Events relating to Baxter products can also be reported direct to Baxter Pharmacovigilance on +44 (0)1635 206360, or by email to email@example.com Drug or medical device product quality complaints relating to Baxter products can be reported directly to Baxter Healthcare Ltd: In the UK +44 (0)1604 704603, or by email to UK_SHS_QA_Complaints@baxter.com. In Ireland on +353 (0)1 2065500 or by email to firstname.lastname@example.org.
Alternatively please report directly to your Baxter Representative, who will take the details and forward to the Baxter Country Quality Assurance Team.
Every day, millions of patients and caregivers rely on Baxter’s leading portfolio of critical, nutritional, renal, hospital and surgical care products and services. For more than 85 years, we’ve been operating at the critical intersection where innovations that save and sustain lives meet the healthcare providers that make it happen. Operating in the UK for over 60 years, Baxter is one of the largest suppliers to the NHS, producing more than 7,500 products and services.