This website is an information resource about Penthrox® intended for healthcare professionals only.
Patients who have been given Penthrox® can find the Patient Information Leaflet (PIL) here.
Report adverse events
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.
Mundipharma routinely monitors the safety of all its medicines, including 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 by calling +44 (0) 1223 424 211 or by emailing firstname.lastname@example.org. Mundipharma will only use your details to contact you about your adverse event report.
Mundipharma International Limited (“We”) are committed to protecting and respecting your privacy.
For the purpose of the Data Protection Act 1998 (the Act), the data controller is Mundipharma International Limited of Cambridge Science Park, Milton Road, Cambridge, CB4 0AB.
We may collect and process the following data about you: