Drug Monograph

Vigabatrin (Sabril)

vigabatrin — irreversible GABA-transaminase inhibitor (γ-vinyl-GABA)

GABA-Transaminase Inhibitor · Oral · REMS Required
Pharmacokinetic Profile
Half-Life
5–8 h (plasma); but duration of effect >> half-life due to irreversible enzyme inhibition
Metabolism
Minimal hepatic; mild CYP2C9 inducer; excreted ~70% unchanged renally
Protein Binding
None (0%)
Bioavailability
~100% (essentially complete oral absorption)
Volume of Distribution
~0.8 L/kg
Black Box Warning
Permanent bilateral concentric visual field constriction (≥30% of adults)
Clinical Information
Drug Class
Irreversible GABA-Transaminase Inhibitor
Available Doses
Tablets: 500 mg; Oral solution: 500 mg packets (reconstituted to 50 mg/mL)
Route
Oral only
Renal Adjustment
Yes: mild −25%, moderate −50%, severe −75%
Hepatic Adjustment
Not studied; minimal hepatic metabolism expected to have limited impact
Pregnancy
Animal data: fetal harm (cleft palate); use only if benefits outweigh risks
Lactation
Excreted in breast milk; breastfeeding not recommended
Schedule / Legal Status
Not a controlled substance; REMS restricted distribution
Generic Available
Yes (Vigafyde and generics)
Rx

Indications

IndicationApproved PopulationTherapy TypeStatus
Refractory complex partial seizures (CPS)≥2 years of ageAdjunctive therapy (not first-line)FDA Approved
Infantile spasms (IS)1 month to 2 years of ageMonotherapyFDA Approved

Vigabatrin occupies a unique position among antiseizure medications as an irreversible enzyme inhibitor with a mechanism fundamentally different from all other ASMs. Its two FDA-approved indications reflect very different clinical scenarios. For refractory complex partial seizures, vigabatrin is strictly a last-resort adjunctive agent reserved for patients who have failed multiple alternatives, because the risk of permanent vision loss precludes its use as an early-line therapy. For infantile spasms, vigabatrin has a more prominent role and is considered one of three first-line options alongside ACTH and oral corticosteroids, particularly in patients with tuberous sclerosis complex (TSC) where response rates are especially high. Due to the risk of permanent vision loss, vigabatrin is available only through the Vigabatrin REMS Program, requiring certified prescribers and pharmacies, patient enrollment, and mandatory periodic vision monitoring.

Off-Label Uses

Succinic semialdehyde dehydrogenase (SSADH) deficiency: Vigabatrin is used in this rare inborn error of GABA metabolism to lower accumulating GHB levels by inhibiting GABA-transaminase. Evidence quality: Low (case series; orphan disease).

Tuberous sclerosis complex (TSC) — seizure types beyond infantile spasms: Some evidence supports vigabatrin for focal seizures in TSC patients of various ages, given the particularly high response rate in this population. Evidence quality: Moderate.

Dose

Dosing

Dosing by Clinical Scenario

Clinical ScenarioStarting DoseMaintenance DoseMaximum DoseNotes
Refractory CPS — adults (≥17 years)1,000 mg/day (500 mg BID)3,000 mg/day (1,500 mg BID)3,000 mg/day (6,000 mg/day has no additional benefit)Increase by 500 mg/day weekly; taper by 1,000 mg/day weekly when discontinuing
Withdraw if no substantial benefit within 3 months
Refractory CPS — pediatric 10–15 kg350 mg/day1,050 mg/day1,050 mg/dayAll pediatric doses given as 2 divided doses; increase weekly
>60 kg: use adult dosing
Refractory CPS — pediatric >15–20 kg450 mg/day1,300 mg/day1,300 mg/dayTaper by one-third every week for 3 weeks when discontinuing
Refractory CPS — pediatric >20–25 kg500 mg/day1,500 mg/day1,500 mg/dayTaper by one-third every week for 3 weeks when discontinuing
Refractory CPS — pediatric >25–60 kg500 mg/day2,000 mg/day2,000 mg/dayTaper by one-third every week for 3 weeks when discontinuing
Infantile spasms — 1 month to 2 years50 mg/kg/day (25 mg/kg BID)Titrate by 25–50 mg/kg/day every 3 days150 mg/kg/day (75 mg/kg BID)Monotherapy; use oral solution reconstituted to 50 mg/mL; withdraw if no substantial benefit within 2–4 weeks
Taper by 25–50 mg/kg every 3–4 days when discontinuing
Renal impairment — adults and ≥2 yearsMild (CrCl >50–80): decrease dose 25% | Moderate (CrCl >30–50): decrease 50% | Severe (CrCl >10–30): decrease 75%Primarily renally eliminated; no data on dose adjustment in infants with renal impairment
Use the Lowest Dose for the Shortest Duration

The risk of permanent vision loss increases with cumulative dose and duration of exposure, and there is no dose or exposure known to be free of risk. The FDA PI mandates using the lowest dosage and shortest exposure consistent with clinical objectives. In refractory CPS, vigabatrin must be withdrawn if no substantial benefit is observed within 3 months. In infantile spasms, treatment should be withdrawn within 2–4 weeks if no response is seen. Patient response and continued need for treatment must be periodically reassessed throughout therapy.

Clinical Pearl: Plasma Level Monitoring Is Not Helpful

Unlike most ASMs, monitoring vigabatrin plasma concentrations does not guide dosing. This is because vigabatrin is an irreversible enzyme inhibitor — its antiseizure effect depends on the rate of new GABA-transaminase synthesis (requiring several days) rather than on the instantaneous drug concentration. The plasma half-life of 5–8 hours dramatically understates the duration of pharmacological effect, which persists for days after the drug has been eliminated. Dose adjustments should be based on clinical response, not plasma levels.

PK

Pharmacology

Mechanism of Action

Vigabatrin is a structural analogue of GABA that functions as an irreversible, mechanism-based inhibitor of GABA-transaminase (GABA-T), the enzyme responsible for the catabolism of the inhibitory neurotransmitter GABA. By permanently inactivating GABA-T, vigabatrin causes a sustained increase in synaptic and extrasynaptic GABA concentrations throughout the brain. The drug is supplied as a racemic mixture, but only the S(+)-enantiomer is pharmacologically active. Because the enzyme inhibition is irreversible, the pharmacological effect persists until new GABA-T enzyme is synthesized, a process that takes several days. This means the antiseizure duration of effect dramatically outlasts the drug's presence in plasma, making the plasma half-life a poor guide to dosing or efficacy. The resulting elevation of inhibitory GABAergic tone is effective across a broad range of seizure types but is particularly potent against infantile spasms, especially in the context of tuberous sclerosis complex.

ADME Profile

ParameterValueClinical Implication
AbsorptionEssentially complete oral absorption (~100%); Tmax 1–2 h (adults), ~2.5 h (infants); food decreases Cmax by 33% but does not alter AUC; linear pharmacokinetics from 0.5–4 gMay be given with or without food; food does not affect total drug exposure. Both tablet and oral solution formulations are bioequivalent
DistributionVd ~0.8 L/kg; no plasma protein binding (0%); enters CSF (CSF levels ~10% of plasma at 6 h post-dose)Zero protein binding means no protein-displacement drug interactions and no binding-related PK variability in hypoalbuminemic patients. Wide tissue distribution
MetabolismNot significantly metabolized; mild inducer of CYP2C9; no active metabolitesMinimal hepatic metabolism explains the lack of CYP-mediated drug interactions. CYP2C9 induction likely accounts for 16–20% decrease in phenytoin levels seen with co-administration
EliminationPlasma t½ 5–8 h (adults), ~5.7 h (infants); ~70% excreted unchanged in urine; renal clearance is the primary elimination pathway; hemodialysis reduces plasma levels by 40–60%; linear kinetics; little accumulation with repeated dosingShort plasma half-life is clinically misleading — pharmacological effect persists for days due to irreversible GABA-T inhibition. Dose reduction essential in renal impairment. Plasma level monitoring is not useful for guiding therapy
SE

Side Effects

The adverse effect profile of vigabatrin is dominated by the risk of permanent, irreversible visual field loss — an effect so significant that it carries an FDA Black Box Warning and mandates a REMS program for distribution. Beyond vision loss, the controlled trial data in adults show somnolence (24% vs 10% placebo), fatigue (28% vs 15%), dizziness, and weight gain as the most common treatment-emergent effects. In pediatric CPS patients, weight gain is the predominant adverse effect (47% gained ≥7% body weight vs 19% placebo).

≥10% Very Common
Adverse EffectIncidenceClinical Note
Fatigue28% vs 15% placebo (adult CPS)Most commonly reported adverse effect; dose-related; advise against driving or operating machinery until familiar with effects
Somnolence24% vs 10% placebo (adult CPS)Dose-related; may be additive with other CNS depressants; less prominent in pediatric CPS trials (6% vs 5%)
Weight gain (≥7% of baseline)17% vs 8% placebo (adults); 47% vs 19% (pediatric CPS)Not related to edema; mean weight gain 3.5 kg vs 1.6 kg (placebo) in adults; long-term effects unknown; monitor weight at each visit
1–10% Common
Adverse EffectIncidenceClinical Note
Blurred vision≥5% over placebo (adult CPS)Most common visual symptom reported; distinct from the visual field constriction in the Black Box Warning; may or may not indicate retinal damage
Dizziness≥5% over placebo (adult CPS)Dose-related CNS effect
Abnormal coordination / tremor≥5% over placebo (adult CPS)Cerebellar/motor effects; assess gait at visits
Anemia6% vs 2% placebo (adults)Mean hemoglobin decrease ~3% vs 0% placebo; monitor for symptoms; rarely clinically significant
Peripheral edema2% vs 1% placebo (adults)Not associated with cardiovascular deterioration or hepatic/renal dysfunction
Peripheral neuropathy4.2% (pooled); 1.4% vs 0% placebo (controlled)Numbness/tingling in toes or feet, decreased vibration sense; reversibility not established
Serious Serious Adverse Effects
Adverse EffectEstimated FrequencyTypical OnsetRequired Action
Permanent bilateral concentric visual field constriction (BLACK BOX)≥30% of adults; poorly characterized in childrenUnpredictable: weeks to years after initiationBaseline vision assessment within 4 weeks; every 3 months during therapy; 3–6 months after discontinuation. Perimetry recommended in cooperative patients; ERG/OCT as adjuncts. Irreversible once detected. Consider discontinuation if vision loss documented. REMS mandatory
Decreased visual acuity (central retinal damage)Occurs in some cases in addition to visual field lossVariableCentral retina can also be damaged; visual acuity testing should be part of monitoring; irreversible
MRI abnormalities in infants (T2 signal changes)22% of vigabatrin-treated infants vs 4% other therapiesDuring treatment (infants with IS)Symmetric T2 signal in thalamus, basal ganglia, brainstem, cerebellum; generally resolves with discontinuation; clinical significance of long-term sequelae unknown
Intramyelinic edema (neurotoxicity)Observed in animal studies at therapeutic doses; reported in postmortem infant examinationsDuring treatmentVacuolation in brain white matter seen in rats, mice, dogs, possibly monkeys; no established no-effect dose in rodents or dogs; MRI monitoring in infants recommended
Suicidal behavior and ideationAED class effect (RR 1.8 vs placebo)As early as 1 weekAED class warning; monitor for depression, mood changes, suicidal ideation at each visit
Discontinuation Withdrawal Considerations
Adults (CPS)
Taper by 1,000 mg/day weekly
Do not stop abruptly. Gradual withdrawal is required to avoid rebound seizures. In controlled trials, the taper schedule decreased daily dose by 1,000 mg/day on a weekly basis until discontinued.
Infants (IS)
Taper by 25–50 mg/kg every 3–4 days
Mandatory withdrawal if no response. Discontinue if no substantial benefit within 2–4 weeks (IS) or 3 months (CPS). Every additional day of exposure increases cumulative vision loss risk.
Vision Loss: The Defining Safety Concern

Vigabatrin causes permanent bilateral concentric visual field constriction in 30% or more of adult patients. Severe cases manifest as tunnel vision to within 10 degrees of fixation, which can be functionally disabling. The onset is unpredictable — from weeks to years — and symptoms are unlikely to be recognized before loss is severe. Vision loss is irreversible once detected, and may worsen even after drug discontinuation. The mechanism is attributed to retinal toxicity via taurine depletion. This risk fundamentally defines vigabatrin's clinical positioning: it should only be used when benefits clearly outweigh this serious risk, and the lowest dose for the shortest possible duration must always be employed.

Int

Drug Interactions

Vigabatrin has a remarkably clean drug interaction profile compared to older enzyme-inducing ASMs. It undergoes minimal hepatic metabolism, has zero protein binding, and does not induce or inhibit most CYP enzymes. The primary interaction of clinical relevance is a modest reduction in phenytoin levels, likely mediated by mild CYP2C9 induction. The FDA PI also notes that vigabatrin decreases amino acid transaminase (AST and ALT) laboratory values as a pharmacodynamic effect of GABA-T inhibition, which can mask detection of hepatic injury from other causes.

Moderate Phenytoin
MechanismVigabatrin induces CYP2C9, which metabolizes phenytoin
EffectPhenytoin plasma levels decreased by 16–20% on average
ManagementDose adjustment of phenytoin not routinely required; consider if clinically indicated based on seizure control and phenytoin levels
FDA PI
Minor Phenobarbital / Primidone
MechanismNot fully elucidated; likely related to metabolism effects
EffectPhenobarbital concentrations reduced by 8–16% on average
ManagementGenerally not clinically significant; monitor levels if seizure control worsens
FDA PI
Minor Sodium Valproate
MechanismNot fully elucidated
EffectValproate plasma concentrations reduced by ~8% on average
ManagementNot clinically relevant in most cases
FDA PI
Moderate AST/ALT Laboratory Test Interference
MechanismGABA-T inhibition also suppresses amino acid transaminase activity, lowering AST and ALT
EffectDecreased AST/ALT values may mask detection of hepatic injury from other causes
ManagementBe aware that normal transaminases in a vigabatrin-treated patient may not exclude hepatic pathology; consider alternative markers (GGT, bilirubin, INR) if liver disease suspected
FDA PI
Minor Clonazepam
MechanismVigabatrin increased clonazepam Cmax by 30% and decreased Tmax by 45% in one PK study
EffectPotentially enhanced sedation with clonazepam
ManagementMonitor for enhanced sedation; clonazepam had no effect on vigabatrin concentrations
FDA PI
Minor Oral Contraceptives
MechanismNo significant interaction expected (vigabatrin does not induce CYP3A4)
EffectVigabatrin is unlikely to affect the efficacy of steroid oral contraceptives
ManagementNo contraceptive adjustment needed — an advantage over enzyme-inducing ASMs
FDA PI
Mon

Monitoring

  • Vision Assessment Baseline (within 4 weeks of start); every 3 months during therapy; 3–6 months after discontinuation
    Routine
    MANDATORY per REMS. Perimetry (preferably automated threshold visual field testing) in cooperative patients. Consider ERG, OCT, or other methods for patients who cannot undergo perimetry. Includes infants where vision assessment should be individualized (visual acuity and visual field when possible). Vision loss may occur or worsen precipitously between assessments. Even with frequent monitoring, some patients will develop severe vision loss.
  • MRI (Infants Only) As clinically indicated during treatment in infants with IS
    Trigger-based
    Abnormal T2 signal changes in thalamus, basal ganglia, brainstem, and cerebellum reported in 22% of vigabatrin-treated infants. Generally resolve with discontinuation. Not required for adults as there is no evidence vigabatrin causes MRI changes in this population.
  • Complete Blood Count Periodically during therapy
    Routine
    Anemia occurs in 6% vs 2% placebo. Mean hemoglobin decrease ~3%. Monitor for symptoms of anemia (fatigue, pallor, dyspnea).
  • Body Weight Each visit
    Routine
    Weight gain ≥7% in 17% adults, 47% pediatric CPS patients. Monitor nutritional counseling and metabolic parameters.
  • Mood and Suicidality Every visit, ongoing
    Routine
    AED class warning for suicidal behavior and ideation. Monitor for depression, unusual mood/behavioral changes.
  • Peripheral Neuropathy Assessment Periodically; if symptoms develop
    Trigger-based
    Numbness, tingling in toes/feet, decreased vibration/position sense, progressive loss of ankle reflexes. Occurred in 4.2% of patients in pooled studies. Reversibility not established.
  • Renal Function Baseline and periodically
    Routine
    Vigabatrin is primarily renally eliminated. Dose reduction required in renal impairment (mild −25%, moderate −50%, severe −75%). Monitor CrCl, especially in elderly patients or those with changing renal function.
  • Treatment Response Assessment CPS: within 3 months of initiation; IS: within 2–4 weeks
    Routine
    Mandatory per FDA PI. Withdraw vigabatrin if no substantial clinical benefit by these timepoints. Patient response and continued need for treatment must be periodically reassessed. Every additional day of unnecessary exposure increases cumulative vision loss risk.
CI

Contraindications & Cautions

Absolute Contraindications

  • None listed in the FDA PI — the FDA label states no absolute contraindications. However, the extensive warnings and REMS program effectively restrict use to situations where benefits clearly outweigh the risk of permanent vision loss.

Relative Contraindications (Specialist Input Recommended)

  • Pre-existing visual field defects or other irreversible vision loss — the interaction of existing vision damage with vigabatrin-induced damage is likely adverse and not well characterized; benefits must clearly outweigh risks
  • Concurrent use of other drugs with serious ophthalmic effects (retinopathy, glaucoma) — additive vision risk; avoid unless benefits clearly outweigh risks
  • Severe renal impairment (CrCl 10–30 mL/min) — 75% dose reduction required; drug accumulation risk
  • Pregnancy — animal data show fetal harm (cleft palate in rabbits at doses near therapeutic range); use only if potential benefits justify potential risks

Use with Caution

  • Nursing mothers — vigabatrin is excreted in human breast milk; breastfeeding is not recommended
  • Elderly patients — delayed absorption, increased peak concentration, and prolonged half-life due to decreased renal clearance; start with reduced doses
  • History of depression or psychiatric illness — AED class warning; rare psychosis reported, more common in adults than children
  • Patients at risk of generalized tonic-clonic seizures — vigabatrin approved only for focal (CPS) and IS; not for primary generalized epilepsy
FDA Boxed Warning Permanent Vision Loss

SABRIL can cause permanent bilateral concentric visual field constriction, including tunnel vision that can result in disability. In some cases, SABRIL also can damage the central retina and may decrease visual acuity. The onset of vision loss is unpredictable, and can occur within weeks of starting treatment or at any time during or after treatment. The risk increases with increasing dose and cumulative exposure, but there is no dose or exposure known to be free of risk. Vision loss due to SABRIL is not reversible. Because of this risk, SABRIL is available only through the Vigabatrin REMS Program.

FDA Class-Wide Regulatory Warning Suicidal Behavior and Ideation — All Antiepileptic Drugs

Antiepileptic drugs, including SABRIL, increase the risk of suicidal thoughts or behavior. Pooled analysis of 199 placebo-controlled trials of 11 AEDs showed approximately twice the risk (adjusted RR 1.8; 95% CI: 1.2–2.7) in AED-treated patients compared to placebo. Monitor all patients for emergence or worsening of depression, suicidal thoughts, or unusual changes in behavior.

Pt

Patient Counselling

Purpose of Therapy

Vigabatrin is a seizure medication that works by increasing the levels of a natural calming chemical (GABA) in the brain. It is used for two specific conditions: infantile spasms in babies (1 month to 2 years) and hard-to-treat focal seizures in patients 2 years and older who have not responded to other seizure medicines. Because vigabatrin carries a risk of permanent vision changes, it is only prescribed when the benefits are expected to outweigh this serious risk.

How to Take

Vigabatrin can be taken with or without food. Tablets should be taken twice daily. For infants and young children, the powder packets must be dissolved in cold or room-temperature water (10 mL per packet) to create a liquid solution (50 mg/mL), which is then measured with an oral syringe. Each dose must be prepared fresh and any unused solution discarded. Do not stop this medication suddenly — your doctor will gradually reduce the dose over several weeks.

Vision Changes (Most Important Concern)
Tell patient Vigabatrin can cause permanent vision loss, including loss of side (peripheral) vision. This can happen at any time during treatment and may not be noticeable until it is severe. You will need regular eye exams — at the start of treatment, every 3 months during treatment, and for 3–6 months after stopping. Even with regular eye exams, vision loss may not be detected early. The risk increases the longer you take this medication.
Call prescriber Immediately if you notice any change in vision, including blurred vision, difficulty seeing to the side, or bumping into objects. Also report any difficulty with night vision or sensitivity to light.
Drowsiness and Fatigue
Tell patient Drowsiness and tiredness are common side effects (affecting up to 1 in 4 adults). Do not drive, operate machinery, or perform activities requiring alertness until you know how vigabatrin affects you. Avoid alcohol and other sedating medications while taking this drug.
Call prescriber If excessive drowsiness interferes with daily functioning or if you feel unsteady or have difficulty with coordination.
Weight Gain
Tell patient Weight gain is a common side effect, particularly in children. Maintain a healthy diet and regular physical activity while on this medication. Report significant changes in appetite or weight to your doctor.
Call prescriber If you experience rapid or excessive weight gain, or if swelling develops in the legs, ankles, or feet.
Numbness or Tingling (Peripheral Neuropathy)
Tell patient Some patients develop numbness, tingling, or reduced sensation in the toes and feet. Report these symptoms to your doctor, as they may indicate nerve damage that could require a change in treatment.
Call prescriber If you notice new numbness or tingling in your feet or toes, difficulty feeling the ground when walking, or progressive loss of sensation in your lower legs.
Ref

Sources

Regulatory (PI / SmPC)
  1. SABRIL (vigabatrin) Tablets and Oral Solution. Full Prescribing Information. NDA 020427/S-025, 022006/S-026. Lundbeck Inc. Revised October 2021. FDA Label Primary US prescribing information for vigabatrin (Sabril), including the Black Box Warning for vision loss, REMS requirements, weight-based pediatric dosing tables, and complete adverse reactions data from controlled trials.
  2. VIGAFYDE (vigabatrin) Oral Solution. Full Prescribing Information. NDA 217684. Revised 2024. FDA Label Prescribing information for the Vigafyde formulation, providing additional pharmacokinetic data including infant Tmax (~2.5 hours) and food effect data.
Key Clinical Trials
  1. Elterman RD, Shields WD, Mansfield KA, Nakagawa J; US Infantile Spasms Vigabatrin Study Group. Randomized trial of vigabatrin in patients with infantile spasms. Neurology. 2001;57(8):1416–1421. doi:10.1212/WNL.57.8.1416 Pivotal US randomized trial demonstrating vigabatrin efficacy for infantile spasms, supporting FDA approval.
  2. French JA, Mosier M, Walker S, Sommerville K, Sussman N; Vigabatrin Protocol 024 Investigative Cohort. A double-blind, placebo-controlled study of vigabatrin three g/day in patients with uncontrolled complex partial seizures. Neurology. 1996;46(1):54–61. doi:10.1212/WNL.46.1.54 Key placebo-controlled trial establishing vigabatrin 3 g/day efficacy for refractory CPS in adults.
  3. Chiron C, Dumas C, Jambaque I, Mumford J, Dulac O. Randomized trial comparing vigabatrin and hydrocortisone in infantile spasms due to tuberous sclerosis. Epilepsy Res. 1997;26(2):389–395. doi:10.1016/S0920-1211(96)01006-6 Landmark study demonstrating vigabatrin superiority over hydrocortisone for infantile spasms in tuberous sclerosis complex (TSC), with high response rates in this population.
Guidelines
  1. Go CY, Mackay MT, Weiss SK, et al; Child Neurology Society. Evidence-based guideline update: medical treatment of infantile spasms. Neurology. 2012;78(24):1974–1980. doi:10.1212/WNL.0b013e318259e2cf AAN/CNS guideline establishing vigabatrin as a Level B treatment for infantile spasms (possibly effective) and Level C for TSC-related spasms.
  2. Glauser T, Ben-Menachem E, Bourgeois B, et al. Updated ILAE evidence review of antiepileptic drug efficacy and effectiveness as initial monotherapy for epileptic seizures and syndromes. Epilepsia. 2013;54(3):551–563. doi:10.1111/epi.12074 ILAE evidence review of ASM efficacy; vigabatrin assessed for infantile spasms and refractory focal epilepsy.
Mechanistic / Basic Science
  1. Jung MJ, Lippert B, Metcalf BW, Böhlen P, Schechter PJ. γ-Vinyl GABA (4-amino-hex-5-enoic acid), a new selective irreversible inhibitor of GABA-T: effects on brain GABA metabolism in mice. J Neurochem. 1977;29(5):797–802. doi:10.1111/j.1471-4159.1977.tb10721.x Original description of vigabatrin (γ-vinyl GABA) as a selective irreversible inhibitor of GABA-transaminase, establishing its mechanism of action.
  2. Duboc A, Hanoteau N, Simonutti M, et al. Vigabatrin, the GABA-transaminase inhibitor, damages cone photoreceptors in rats. Ann Neurol. 2004;55(5):695–705. doi:10.1002/ana.20081 Key study demonstrating the retinal toxicity mechanism of vigabatrin, showing cone photoreceptor damage and taurine depletion as the likely basis for visual field loss.
  3. Vigabatrin. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024. StatPearls Comprehensive clinical pharmacology reference covering mechanism of action, dosing, pharmacokinetics, vision loss risk, and monitoring requirements.
Pharmacokinetics / Special Populations
  1. Rey E, Pons G, Olive G. Vigabatrin: clinical pharmacokinetics. Clin Pharmacokinet. 1992;23(4):267–278. doi:10.2165/00003088-199223040-00003 Definitive pharmacokinetic review establishing vigabatrin PK parameters: Vd ~0.8 L/kg, zero protein binding, half-life 5.3–7.4 hours, ~70% renal excretion unchanged, and linear dose-proportional kinetics.
  2. Krauss G, Faught E, Foroozan R, et al. Sabril registry 5-year results: characteristics of adult patients treated with vigabatrin. Epilepsy Behav. 2016;56:15–19. doi:10.1016/j.yebeh.2015.12.025 Sabril post-marketing registry providing long-term safety data on vision monitoring and visual field outcomes in adult patients treated with vigabatrin.