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| ftk = valproinezuur
| ATC = N03AG01
| administration metabolization = OralValproic acid is principally metabolized by CYP2C9, rectal| ctox = 150000| ctox_ref = <ref name="ftktox">{{ftktox}}</ref>| cth = | halflife = 10CYP2C19, CYP2A6 and UDP-glucuronosyltransferases. Valproic acid is an inhibitor of the enzymes CYP2C9, epoxide-hydroxylase and UDP-15| halflife_ref = glucuronosyltransferases.<ref name="ftk">{{FTK|valproinezuur}}</ref>| metabolites = 1| metabolites_ref = <ref name="ftk" />
<includeonly>
| isswitch = 1
</includeonly>
}}