This promotional material is intended for UK Healthcare Professionals (HCPs) experienced in the diagnosis and management of Parkinson’s disease only. Adverse event reporting can be found below
Some patients may not be suitable for PRODUODOPA. You are strongly advised to read the Prescribing Information (PI), and Summary of Product Characteristics (SmPC) which can be found via the links above, to evaluate patient suitability for PRODUODOPA.
These promotional events are intended for UK healthcare professionals experienced in the diagnosis and management of advanced Parkinson's disease only.
They have been organised and funded by AbbVie, including payment of speaker honoraria, and will contain information about Produodopa®.
Welcome to the exPloreD events page where you can register for the events of your choice.
Please click on the event you would like to register for and you will be taken to the specific registration page. You can register for more than one event.
Promotional Training Meetings 2025
AbbVie invites you to register for these promotional training meetings, where you will be guided through initiating Produodopa® using Vyafuser pump for appropriate patients.
In-Person 2-Day Promotional Masterclass
AbbVie invites you to register for this educational promotional masterclass, where you will have the opportunity to learn more about the role of Produodopa® in clinical practice for advanced Parkinson's Disease. The sessions will cover topics such as patient identification, on-going management and service considerations with a panel of experts and interactive workshops.
Please refer to the PRODUODOPA SmPC for further information on adverse events, contraindications and special warnings and precautions for use.
References
- PRODUODOPA (foslevodopa/foscarbidopa solution for infusion) Summary of Product Characteristics.
By clicking the link above you will leave the AbbVie Pro website and be taken to the eMC PI portal website
Adverse events should be reported. Reporting forms and information can be found at yellowcard.mhra.gov.uk.
Adverse events should also be reported to AbbVie on GBPV@abbvie.com
UK-PRODD-250064. Date of preparation: March 2025.