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In our case series we relied primarily on postmarketing safety reports that are voluntarily submitted to the US Food and Drug Administration's Adverse Event Reporting System database.

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Veröffentlicht in:Journal of allergy and clinical immunology 2008-03, Vol.121 (3), p.786
Hauptverfasser: Limb, Susan L, Lee, Charles E, Starke, Peter R, Chowdhury, Badrul A
Format: Artikel
Sprache:eng
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Zusammenfassung:In our case series we relied primarily on postmarketing safety reports that are voluntarily submitted to the US Food and Drug Administration's Adverse Event Reporting System database.
ISSN:0091-6749
1097-6825
DOI:10.1016/j.jaci.2007.12.1187