Drug data last refreshed 2d ago
SABRIL (vigabatrin) is an oral anti-epileptic agent approved by the FDA in August 2009 and marketed by Lundbeck. It is indicated for the treatment of seizure disorders, functioning as a unique mechanism anti-epileptic drug. Vigabatrin irreversibly inhibits GABA transaminase, increasing GABA concentrations in the central nervous system. The product represents a specialized therapy within the anti-epileptic drug class, typically reserved for specific seizure types due to its safety profile.
Anti-epileptic Agent
Indication data is being enriched from DailyMed and FDA labeling. Check back soon for approved therapeutic uses.
An Open-Label, Single and Multiple Oral Dose Pharmacokinetic Study of Vigabatrin in Infants With Infantile Spasms
Vigabatrin for the Treatment of Cocaine Dependency
A Study of the Structure and Function of the Retina in Adult Patients With Refractory Complex Partial Seizures Treated With Vigabatrin (Sabril®)
Sabril for Complex Partial Seizures in Adult Tolerability Study (TS) Patients
Sabril Patient Registry
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The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.
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Upgrade to Pro — $25/moCurrently zero open positions are linked to this product in available job databases. As SABRIL approaches loss of exclusivity, career opportunities may contract, with remaining roles likely focused on specialty/neurology sales representatives and medical science liaisons serving neurologists. Success in this product space requires deep expertise in epilepsy management, knowledge of restricted seizure indications, and ability to work within a contracting commercial footprint.