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- W1997184549 abstract "In February 2009, the European Medicines Agency's (EMEA) Committee for Medicinal Products for Human Use (CHMP) had recommended the suspension of efalizumab's (Raptiva) marketing authorization, because its benefits in the treatment of psoriasis were modest, while there was a risk of serious side effects in patients receiving the medicine, including the occurrence of progressive multifocal leukoencephalopathy (PML). The guideline group has changed the guideline accordingly." @default.
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- W1997184549 date "2009-12-23" @default.
- W1997184549 modified "2023-10-17" @default.
- W1997184549 title "S3-Leitlinie zur Therapie der Psoriasis vulgaris - Update: „Übersicht der Therapieoptionen” und „Efalizumab”" @default.
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- W1997184549 doi "https://doi.org/10.1111/j.1610-0387.2009.07312_supp.x" @default.
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