Living with Parkinson’s

Hi I have had a Vylex Produadopa pump since September 2024 just after they were approved by NICE in the UK. It transformed my life from being housebound and in pain and gave me my life back by controlling my symptoms and giving me hour and hours of On time. The pump is challenging to manage on a daily basis I won’t lie, but the effect it had on managing my symptoms was like a miracle, so worth it. The Produadopa vials had always contained a pink solution until in December I was delivered a white coloured Produadopa. The leaflet says it can have vary in colour, this was not a variation it was a totally different colour. I used them and immediately had a return of symptoms and pooling and burning at canular site. AbbVie insisted there is no difference in effectiveness between colours, for me there definitely is. I found out there are 3 colours: Pink: White: Dark Amber all totally different in colour and for me anything but Pink does not control my symptoms. I have just had a delivery and now there is a 4th colour, these are Yellow. My condition has gone from being independent and happy to housebound, symptomatic and miserable again. My opinion about a difference in effectiveness is ignored. I know by my bodies physical reaction the colours are different.

Has anyone else had a similar experience with receiving different coloured Produadopa and noticed a difference in effectiveness?

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Good question - sorry I don’t have the answer but I can’t believe there’s no reason for the different colours!

You might like to ask the question over on Health Unlocked - Cure Parkinson’s Trust site. I know that they have a lot of active users of this device over there!

Best rgds

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Hi @Jan_Fuller, welcome to the community. Thank you so much for sharing your experience - it sounds like it’s been a real journey, and we’re so glad the pump initially made such a positive difference for you.

I’m really sorry to hear how things have changed more recently - that sounds incredibly frustrating and upsetting, especially when you know your own body so well. You’re absolutely right to raise this.

It would be really important to speak to your Parkinson’s specialist or nurse about what you’re experiencing, as well as your pharmacist or the medication provider, so they can look into this further with you.

Hopefully others here will also share their experiences, but you’re not alone in this. If it would help to talk things through, our free and confidential helpline is here for you too: 0808 800 0303. :blue_heart:

Parkinson’s UK Moderation Team

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