This app is intended for adult patients who have been prescribed Perampanel Eisai (perampanel) tablets in the UK
myCompi
What is it about?
This app is intended for adult patients who have been prescribed Perampanel Eisai (perampanel) tablets in the UK. This app has been initiated and funded by Eisai Pharmaceuticals Ltd. This app is easy to set up and provides adult patients in the UK with useful information on how to get started on their treatment. It also allows patients to set their own reminders for appointments with their doctor and for when to take their medication. The app contains resources, frequently asked questions, video content and key information about the medication the adult patient has been prescribed. In order to access the app, the adult patient will have been provided with an access code from their healthcare professional. The data collected in this application is stored locally in this device.
App Store Description
This app is intended for adult patients who have been prescribed Perampanel Eisai (perampanel) tablets in the UK. This app has been initiated and funded by Eisai Pharmaceuticals Ltd. This app is easy to set up and provides adult patients in the UK with useful information on how to get started on their treatment. It also allows patients to set their own reminders for appointments with their doctor and for when to take their medication. The app contains resources, frequently asked questions, video content and key information about the medication the adult patient has been prescribed. In order to access the app, the adult patient will have been provided with an access code from their healthcare professional. The data collected in this application is stored locally in this device.
Reporting of side effects
If you experience any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects not listed in the package leaflet. You can also report side effects directly via the Yellow Card Scheme at https://yellowcard.mhra.gov.uk/. By reporting side effects, you can help provide more information on the safety of this medicine.
UK-FYC-25-00007 March 2025
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