Report an Adverse Event

Thank you for choosing to report a side effect.

In accordance with applicable laws, Mundipharma routinely monitors the safety of all its medicines, including reviewing safety data from clinical studies and collecting reports of adverse events. This information contributes to the continuing safety surveillance of our products.

If you become aware of a patient in the UK who has experienced an adverse event, overdose or unexpected benefits with one of our products, including any possible side effects not listed in the package leaflet, you can report side effects directly via the Yellow Card Scheme at www.mhra.gov.uk/yellowcard. You can also contact Mundipharma by calling +44 (0) 1223 424 211 or by emailing drugsafetyUK@napp.co.uk. Mundipharma will only use your details to contact you about your adverse event report.

If you are a HCP outside of the UK, adverse events should be reported to your local Regulatory Authority or local responsible company, in accordance with local requirements.

Data privacy – Any information and personal data you share with us in relation to side effects 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 see our Privacy Notice.

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