Unauthorised medicines on sale in Ireland - U-Dream Full Night and U-Dream Lite marketed as herbal sleep aid products

News Category: Regulatory news

Date: 10/01/2020

Consumers urged to seek medical advice on stopping use

The HPRA is advising the public that U-Dream Full Night and U-Dream Lite, marketed as herbal sleep aid products, have been found to contain an undeclared substance that is similar to zopiclone, a prescription only medicine. It is known that zopiclone can cause drowsiness, dizziness and abnormal sleep behaviours. The HPRA is advising anyone who purchased and is currently taking either product to consult with their doctor immediately. Anyone who may have recently stopped taking the product and who has health concerns, should also seek medical advice.

U Dream product image

Although these products are not authorised for sale in Ireland, the HPRA has become aware that packs of U-Dream Full Night and U-Dream Lite have been sold to consumers in Ireland from retail outlets, including health stores. It is also possible that some consumers may have purchased either of these products online. As part of an ongoing investigation, the HPRA is identifying these stores and any online outlets to ensure that packs are removed from sale.

The HPRA states that U-Dream Full Night and U-Dream Lite could cause adverse reactions, including if stopped abruptly. Therefore, it is recommended that anyone taking either product should consult with their doctor immediately. Anyone taking either of these products is also advised not to drive, operate machinery or perform other activities requiring mental alertness until they have safely stopped taking this product following consultation with their doctor.

For those who have purchased either of the products, it is advised that they return it to the store from which it was purchased, or, in the case of an online purchase, contact the website.

The HPRA’s investigation is ongoing and updates will be published as necessary. The testing of these products was carried out in Canada and the United States and the products have been recalled from those markets.

If you have experienced an adverse reaction as a result of taking either of these products, a report can be made to the HPRA. Contact details and online and downloadable report forms are available at www.hpra.ie/report

Any other information on the availability of the product in Ireland should be reported to the HPRA on 01 676 4971 or reportacase@hpra.ie 



Weber Shandwick PR:      (01) 679 8600       

Siobhan Molloy / Vicky Jago:      (086) 817 5066 / 087 636 9724 

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