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{{Drug
| name = valproic Valproic acid
| group = anticonvulsant
| wikipedia = valproic_acid
| medscape = 8885
| ftk = valproinezuur
| ATC = N03AG01
| metabolization = * Valproic acid is principally metabolized by CYP2C9, CYP2C19, CYP2A6 and UDP-glucuronosyltransferases. Valproic acid is an inhibitor of the enzymes CYP2C9, epoxide-hydroxylase and UDP-glucuronosyltransferases.| metabolization_ref = <ref name="ftk">{{FTK|valproinezuur}}</ref>| administration = O,R| ctox = 150000| ctox_ref = <ref name="ftktox">{{ftktox}}</ref>| cth = 50000-100000| halflife = 10-15| halflife_ref = <ref name="ftk">{{FTK|valproinezuur}}</ref>| bioavailability = 100| bioavailability_ref = <ref name="informatorium">{{KNMP|valproaat}}</ref>
| <includeonly> isswitch = 1</includeonly>
}}
