ATTENTION:
The European Medicines Agency (EMEA) has come to the decision that the risks of Raptiva (Efalizumab) outweigh its benefits and that the marketing authorisation for this medicine should be suspended in the EU. Therefore the British Association of Dermatologists have decided to remove the Efalizumab Patient Information Leaflet. For more information, please visit the EMEA website for their press release:
www.emea.europa.eu/humandocs/PDFs/EPAR/raptiva/2085709en.pdf
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