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Diacomit contains 250 mg stiripentol
Diacomit <sup>®</sup>contains 250 mg [[stiripentol]]<ref>http://www.ema.europa.eu/docs/es_ES/document_library/EPAR_-_Product_Information/human/000664/WC500036518.pdf</ref><ref>A new type of anticonvulsant, stiripentol. Pharmacological profile and neurochemical study. Arzneimittelforschung. 1984; 34(2):199-204.</ref>


Dravet Syndrome does not exist data
<ref>[http://onlinelibrary.wiley.com/doi/10.1111/j.1528-1167.2006.00497.x/pdf Stiripentol, a Putative Antiepileptic Drug, Enhances the Duration of Opening of GABA<sub>A</sub>-Receptor Channels]</ref>
<gallery>File:(±)-Stiripentol Structural Formulae V.1.svg.png</gallery>
 
 
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%27s_syndrome|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 [[clobazam]]<ref>[http://www.epilepsybehavior.com/article/S1525-5050(14)00698-2/pdf Aras et al 2015]</ref>
 
==ATC==
 
http://www.whocc.no/atc_ddd_index/?code=N03AX17
 
{{refs}}
 
[[Category:GABAA_receptor_positive_allosteric_modulator]]

Revision as of 21:53, 26 February 2019

Diacomit ®contains 250 mg stiripentol[1][2]

[3]


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 clobazam[4]

ATC

http://www.whocc.no/atc_ddd_index/?code=N03AX17

References

References: