Foetal Valproate Spectrum Disorder
The question
To ask the Secretary of State for Health and Social Care, if he will make an assessment of the potential merits of implementing a national redress scheme for (a) mothers and (b) children living with fetal valproate syndrome.
Answered by Ashley Dalton
The Government is carefully considering the valuable work done by the Patient Safety Commissioner and the resulting Hughes Report, which set out options for redress for those harmed by valproate and pelvic mesh. We will be providing an update to the Patient Safety Commissioner’s report at the earliest opportunity. Although the Hughes Report and its recommendations only cover patients harmed in England, the Government recognises that any response will likely have implications for Northern Ireland and is engaging with the Minister for Health in the Northern Ireland Executive on the Hughes Report.
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