Penthrox® Europe
Penthrox® Europe

This website is an information resource intended for healthcare professionals only.

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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 eudrugsafety@mundipharma-rd.eu. Mundipharma will only use your details to contact you about your adverse event report.

Penthrox is a registered trademark of Medical Developments International Limited and is used under licence. The Mundipharma network of independent associated companies has exclusive rights in 40 European countries, but excluding the UK and Ireland.

Copyright © 2018 Mundipharma International Limited. All rights reserved.

Mundipharma

Report an adverse event

Healthcare Professionals

Adverse events should be reported to your local Regulatory Authority in accordance with local requirements.

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 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 eudrugsafety@mundipharma-rd.eu. Mundipharma will only use your details to contact you about your adverse event report.