Safety considerations selecting antiseizure medications for the treatment of individuals with Dravet syndrome

Author:

Nabbout Rima12ORCID,Chemaly N12,Chiron C13ORCID,Kuchenbuch M.12ORCID

Affiliation:

1. Reference Centre for Rare Epilepsies, Department of Pediatric Neurology, Necker Enfants Malades University Hospital, Université De Paris, Paris, France

2. Institut National De La Santé Et De La Recherche Médicale (INSERM), UMR 1163, Institut Imagine, Université De Paris, Paris, France

3. INSERM U1141, Paris, France & Neurospin, CEA, Gif/Yvette, France

Publisher

Informa UK Limited

Subject

Pharmacology (medical),General Medicine

Reference132 articles.

1. Orphan medicinal products in Europe and United States to cover needs of patients with rare diseases: an increased common effort is to be foreseen

2. The European Commission. Communication from the commission—guideline on aspects of the application of article 8(2) of regulation (EC) No 141/2000: review of the period of market exclusivity of orphan medicinal products [Internet]. 2008 [cited 2021 Feb 19. Available from: https://eur-lex.europa.eu/LexUriServ/LexUriServ.do?uri=OJ:C:2008:242:0008:0011:EN:PDF.

3. US Food and Drug Administration. Developing products for rare diseases [internet]. off. comm. 2017 [cited 2021 Feb 19]. p. 8–9. Available from: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2018/206709Orig1s000%2C207223Orig1s000MedR.pdf.

4. The core Dravet syndrome phenotype

5. ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology

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