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tocofersolan (Vedrop®)

 

Following non-submission

AWMSG advice

Status: Not endorsed (Statement of Advice)

In the absence of a submission from the holder of the marketing authorisation, tocofersolan (Vedrop®) cannot be endorsed for use within NHS Wales for the treatment of vitamin E deficiency due to digestive malabsorption in paediatric patients suffering from congenital chronic cholestasis or hereditary chronic cholestasis, from birth (in term newborns) to 16 or 18 years of age, depending on the region.

 Statement of Advice (SOA): tocofersolan (Vedrop) 1180 (PDF, 43Kb)

Medicine details

Medicine name tocofersolan (Vedrop®)
Formulation 50 mg/ml oral solution
Reference number 1180
Indication

For the treatment of vitamin E deficiency due to digestive malabsorption in paediatric patients suffering from congenital chronic cholestasis or hereditary chronic cholestasis, from birth (in term newborns) to 16 or 18 years of age, depending on the region.

Company Orphan Europe (UK) Ltd
BNF chapter Nutrition & blood
Assessment type Non-submission
Status Not endorsed (Statement of Advice)
AWMSG meeting date 13/10/2011
Ratification by Welsh Government 11/10/2011
Date of issue 13/10/2011
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