Report an adverse event

PATIENTS

Thank you for choosing to report a side effect.

If you get any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in the package leaflet. By reporting side effects, you can help provide more information on the safety of medicine.

In the UK, you can report side effects directly via the Yellow Card Scheme at www.mhra.gov.uk/yellowcard.

HCPs

In the UK, you can report side effects directly via the Yellow Card Scheme at www.mhra.gov.uk/yellowcard.

Outside of the UK, adverse events should be reported to your local Regulatory Authority in accordance with local requirements.

 

Mundipharma Research and certain companies within the Mundipharma global network of independent associated companies are required by law to collect certain minimum information relating to persons who have suffered an adverse event or potential adverse reaction to the company’s medicinal product in order to monitor the safety of its medicinal products. This includes reviewing safety data from clinical studies and collecting reports of adverse events.

If you are a patient or are aware of a patient who has experienced an adverse event, overdose or unexpected benefits with one of our products, please also contact Mundipharma Research by calling +44 (0) 1223 424 211 or by emailing [email protected]

All the information and personal data you share with us will be protected and kept confidential in line with our Data Privacy Policy and local regulations and guidance. Your information will be used for the purpose of drug safety surveillance and to enable us to deal with your enquiry appropriately. It may be shared with health authorities and other third parties who are also responsible for drug safety surveillance. If you are a patient, you can ask someone else (e.g. your GP) to send the report if you do not wish to give us your name. For more information about how we protect your personal data, please click here.