An adverse event (or side effect) is any unwanted medical occurrence in a patient who has been given a pharmaceutical product. This can be any unfavourable and unintended sign, symptom or disease associated with the use of the product. Adverse events should be reported.
If you experience a side effect that causes you concern, please tell your healthcare professional immediately.
Patients and healthcare professionals should report adverse events to the Medicines and Healthcare Products Regulatory Authority (MHRA). Reporting forms and information can be found on the MHRA website.
To report an adverse event in a patient taking a Sandoz product in the UK, call +44 (0)845 601 1387 or email [email protected]. Alternatively, please complete the form below.