This is a pilot trial of a single loading dose of vigabatrin in post-anoxic status epilepticus.
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Primary Pharmacologic Outcome - Absorption
Timeframe: 3h
Primary Feasibility Outcome - Enrollment and Drug Delivery
Timeframe: 48 hours
Primary Feasibility Outcome - Visual Screening (Goldmann Perimetry)
Timeframe: 6 months
Primary Feasibility Outcome - Participants With Visual Screening for Taurine Levels
Timeframe: 0h, 72h and 168h following vigabatrin administration