Drug interaction classified as: synergy
Source: DDInter
Antiepileptic
Also known as Tiagabine hydrochloride monohydrate
Tiagabine selectively inhibits the GABA transporter GAT-1, which is responsible for reuptake of synaptically released GABA back into neurons and glia. By blocking GAT-1, tiagabine prolongs the presence of GABA in the synaptic cleft, enhancing GABAergic inhibitory neurotransmission. This mechanism is distinct from other GABAergic anticonvulsants: benzodiazepines enhance GABA receptor sensitivity, barbiturates prolong channel opening, and vigabatrin inhibits GABA catabolism — only tiagabine specifically targets GABA reuptake.
Drug interaction classified as: synergy
Source: DDInter
Clinical effect not specified
Source: DDInter
Clinical effect not specified
Source: DDInter
Tiagabine's half-life is shortened by 2 to 3 hours.
Source: DDInter
8 additional low-confidence interactions hidden — those rows lack a documented mechanism or management plan in our sources.
Continue into a citation-backed clinical answer with the drug context already attached.
Sources: KD Tripathi 7e, Goodman & Gilman 14e, Katzung·Verified: 2026-05-10 · House clinical team