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Diacomit: Difference between revisions
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In December 2001 the European Medicines Agency (EMA) granted stiripentol orphan drug status (designation number EU/3/01/071) for the treatment of severe myoclonic epilepsy of infancy (Dravet's syndrome). On 4 January 2007, the EMA granted the drug a marketing authorisation that is valid throughout the European Union | In December 2001 the European Medicines Agency (EMA) granted stiripentol orphan drug status (designation number EU/3/01/071) for the treatment of severe myoclonic epilepsy of infancy (Dravet's syndrome). On 4 January 2007, the EMA granted the drug a marketing authorisation that is valid throughout the European Union | ||
[[Dravet's | [[Dravet's syndrome]] | ||
does not exist data for combined therapy both valproic acid or cloabazam<ref>Aras et al 2015</ref> | does not exist data for combined therapy both valproic acid or cloabazam<ref>Aras et al 2015</ref> | ||
==ATC== | ==ATC== |
Revision as of 19:06, 31 March 2016
Diacomit contains 250 mg stiripentol[1]
In December 2001 the European Medicines Agency (EMA) granted stiripentol orphan drug status (designation number EU/3/01/071) for the treatment of severe myoclonic epilepsy of infancy (Dravet's syndrome). On 4 January 2007, the EMA granted the drug a marketing authorisation that is valid throughout the European Union
Dravet's syndrome
does not exist data for combined therapy both valproic acid or cloabazam[2]