Levetiracetam Oral side effects: what 77,009 FDA adverse event reports show
Drug class
Not stated in label
Who reports
77,009 reports · 89% serious · 7,088 with death outcome · 54% female
Used for
Levetiracetam is indicated for the treatment of partial-onset seizures in patients 1 month of age and older ( 1.1 ) Levetiracetam is indicated for adjunctive therapy for the treatment of: Myoclonic seizures in patients 12 years of age and older with ju.
What it is
Levetiracetam is an antiepileptic drug available as 500 mg (white), 750 mg (white) and 1000 mg (white) tablets for oral administration.
Boxed warning
None in the current label
Causality screen of the 40 strongest signals
What the badges mean
- Labeled adverse reaction The exact term appears in the label's warnings or adverse-reactions sections: a known, expected effect. The FAERS signal confirms the label rather than discovering anything.
- Labeled (related wording) The label describes this effect under different wording (e.g. 'neutropenia' for 'neutrophil count decreased'). Treated as known.
- Likely indication confounding The term appears in the label's indications: reports probably describe the disease being treated (or its progression), not a drug effect. Classic confounding by indication.
- Reporting / coding artifact An administrative, monitoring or exposure term (product issue, off-label use, 'test normal', overdose...). Not a biological reaction; a high PRR here reflects how reports are coded.
- Lab value / disease marker A laboratory result, investigation or disease-activity marker (antibody positive, CRP abnormal, swollen joint count) not described in the label. These usually mirror the monitored disease or testing protocol rather than a drug effect; not screened further.
- Not in label — unassessed Not found in the label text, not an artifact pattern. This is a genuine candidate for a formal causality assessment (Bradford Hill / WHO-UMC); it has NOT had one here.
Strongest disproportionality signals
Flagged terms (PRR ≥ 2, χ² ≥ 4, n ≥ 10), ranked by PRR; infinite PRRs (no comparator reports) excluded. The EBGM column is a second, shrinkage-based estimate (MGPS) with its 5th percentile EB05 and the BCPNN IC025; a pair flagged by PRR alone is marked PRR-only and should be read as fragile. The strata column recomputes the PRR on serious reports only (and, for the 300 most-reported drugs, adjusted for age band), and flags pairs whose reports are unusually skewed by sex or come mostly from consumers. Each row also shows the PRR against the other drugs of the same FDA class, which removes most confounding by the condition being treated, and a calibrated p-value: on validation, known non-causes average an ROR of about 2, so significance is judged against that empirical null (✓ = p < 0.05 after calibration). 1,253 further terms are in the interactive explorer. Reaction links open the term's cross-drug page.
| Reaction | Reports | PRR 95% CI · ROR · χ²/p | EBGM EB05 · IC025 | Label screen | Serious-only & strata | Trial cross-check |
|---|---|---|---|---|---|---|
| New onset refractory status epilepticus | 56 | 305.9 208.5–448.8ROR 306.1 · calibrated p 4e-11 ✓ | 136.7 EB05 109.2 · IC025 +5.5 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=56 · 100% clinician | not reported in cached trials |
| Tuberous sclerosis complex | 49 | 242.9 165.0–357.5ROR 243.0 · calibrated p 3e-10 ✓ | 121.8 EB05 95.8 · IC025 +5.3 3/3 methods agree | Not in label — unassessed | serious n=49 · 100% clinician | not reported in cached trials |
| Postictal psychosis | 71 | 231.7 168.7–318.4ROR 232.0 · calibrated p 3e-10 ✓ | 120.7 EB05 98.9 · IC025 +5.7 3/3 methods agree | Not in label — unassessed | serious n=71 · ♀ 0% (drug 54%) · 100% clinician | not reported in cached trials |
| Multiple-drug resistance | 1,282 | 193.6 180.3–208.0ROR 196.9 · calibrated p 5e-10 ✓ | 112.6 EB05 107.5 · IC025 +6.7 3/3 methods agree | Reporting / coding artifact | serious n=955 · 94% clinician | not reported in cached trials |
| Epileptic encephalopathy | 90 | 188.2 143.7–246.4ROR 188.4 · calibrated p 1e-9 ✓ | 108.4 EB05 90.9 · IC025 +5.8 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=89 | not reported in cached trials |
| Psychogenic seizure | 259 | 106.3 92.1–122.8ROR 106.7 · calibrated p 8e-8 ✓ | 76.0 EB05 68.5 · IC025 +5.9 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=248 · 100% clinician | not reported in cached trials |
| Change in seizure presentation | 175 | 99.0 83.3–117.8ROR 99.2 · calibrated p 1e-7 ✓ | 72.0 EB05 63.5 · IC025 +5.7 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=172 | not reported in cached trials |
| Focal dyscognitive seizures | 300 | 97.0 85.0–110.6ROR 97.3 · calibrated p 2e-7 ✓ | 71.1 EB05 64.6 · IC025 +5.8 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=297 | not reported in cached trials |
| Partial seizures with secondary generalisation | 122 | 95.8 77.9–117.7ROR 95.9 · calibrated p 2e-7 ✓ | 70.0 EB05 60.2 · IC025 +5.5 3/3 methods agree | Labeled (related wording) related wording | serious n=122 · 93% clinician | not reported in cached trials |
| Anticoagulation drug level abnormal | 39 | 94.9 65.9–136.7ROR 94.9 · calibrated p 4e-7 ✓ | 68.1 EB05 52.0 · IC025 +4.7 3/3 methods agree | Lab value / disease marker | serious n=39 · ♀ 0% (drug 54%) · 100% clinician | not reported in cached trials |
| Sudden unexplained death in epilepsy | 135 | 90.6 74.5–110.1ROR 90.7 · calibrated p 3e-7 ✓ | 67.3 EB05 58.3 · IC025 +5.5 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=135 · 100% clinician | not reported in cached trials |
| Myoclonic epilepsy | 302 | 70.2 61.8–79.6ROR 70.4 · calibrated p 2e-6 ✓ | 55.6 EB05 50.5 · IC025 +5.5 3/3 methods agree | Likely indication confounding term in indications; also in warnings | serious n=302 | not reported in cached trials |
| Postictal paralysis | 47 | 65.5 47.6–90.1ROR 65.6 · calibrated p 4e-6 ✓ | 51.8 EB05 40.5 · IC025 +4.6 3/3 methods agree | Not in label — unassessed | serious n=47 · 100% clinician | NCT01960075: 1/150 (0.7%) on Levetiracetam Oral |
| Status epilepticus | 2,084 | 61.4 58.6–64.4ROR 63.1 · calibrated p 3e-6 ✓ | 50.1 EB05 48.3 · IC025 +5.6 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 32.6 · 91% clinician | NCT00537238: 2/255 (0.8%) on Levetiracetam Oral (serious AE) |
| Partial seizures | 927 | 59.6 55.5–64.0ROR 60.3 · calibrated p 4e-6 ✓ | 48.9 EB05 46.3 · IC025 +5.5 3/3 methods agree | Labeled adverse reaction exact term | serious n=919 | NCT00537238: 1/255 (0.4%) on Levetiracetam Oral (serious AE) |
| Anticonvulsant drug level above therapeutic | 110 | 55.1 44.9–67.7ROR 55.2 · calibrated p 9e-6 ✓ | 45.5 EB05 38.8 · IC025 +4.9 3/3 methods agree | Lab value / disease marker | serious n=108 · 100% clinician | not reported in cached trials |
| Seizure cluster | 132 | 53.4 44.3–64.3ROR 53.5 · calibrated p 1e-5 ✓ | 44.4 EB05 38.4 · IC025 +5.0 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=127 | not reported in cached trials |
| Atonic seizures | 119 | 47.7 39.2–57.9ROR 47.8 · calibrated p 2e-5 ✓ | 40.4 EB05 34.6 · IC025 +4.8 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=117 | not reported in cached trials |
| Simple partial seizures | 120 | 46.8 38.6–56.8ROR 46.9 · calibrated p 2e-5 ✓ | 39.8 EB05 34.1 · IC025 +4.8 3/3 methods agree | Labeled (related wording) related wording | serious n=117 | not reported in cached trials |
| Temporal lobe epilepsy | 63 | 45.3 34.7–59.2ROR 45.4 · calibrated p 3e-5 ✓ | 38.5 EB05 31.2 · IC025 +4.5 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=64 | not reported in cached trials |
| Intensive care unit acquired weakness | 54 | 44.7 33.5–59.7ROR 44.8 · calibrated p 4e-5 ✓ | 38.0 EB05 30.2 · IC025 +4.4 3/3 methods agree | Not in label — unassessed | serious n=54 · ♀ 31% (drug 54%) · 100% clinician | not reported in cached trials |
| Infantile spasms | 99 | 43.7 35.3–54.0ROR 43.7 · calibrated p 4e-5 ✓ | 37.4 EB05 31.6 · IC025 +4.7 3/3 methods agree | Not in label — unassessed | serious n=98 | not reported in cached trials |
| Deja vu | 37 | 42.7 30.2–60.4ROR 42.7 · calibrated p 6e-5 ✓ | 36.3 EB05 27.5 · IC025 +4.1 3/3 methods agree | Not in label — unassessed | serious n=34 | not reported in cached trials |
| Vagal nerve stimulator implantation | 39 | 41.1 29.3–57.6ROR 41.1 · calibrated p 7e-5 ✓ | 35.2 EB05 26.9 · IC025 +4.1 3/3 methods agree | Not in label — unassessed | serious n=37 · 100% consumer | not reported in cached trials |
| Petit mal epilepsy | 655 | 40.2 37.0–43.6ROR 40.5 · calibrated p 5e-5 ✓ | 35.0 EB05 32.8 · IC025 +5.0 3/3 methods agree | Labeled (related wording) related wording | serious n=650 | not reported in cached trials |
| Tonic convulsion | 177 | 39.2 33.5–45.9ROR 39.3 · calibrated p 6e-5 ✓ | 34.2 EB05 30.2 · IC025 +4.7 3/3 methods agree | Not in label — unassessed | serious n=174 | not reported in cached trials |
| Propofol infusion syndrome | 88 | 38.7 30.9–48.4ROR 38.7 · calibrated p 8e-5 ✓ | 33.7 EB05 28.2 · IC025 +4.5 3/3 methods agree | Not in label — unassessed | serious n=88 · 100% clinician | not reported in cached trials |
| Generalised tonic-clonic seizure | 2,032 | 38.5 36.8–40.3ROR 39.5 · calibrated p 6e-5 ✓ | 33.8 EB05 32.6 · IC025 +5.0 3/3 methods agree | Likely indication confounding term in indications; also in warnings | serious PRR 22.2 | not reported in cached trials |
| Anticonvulsant drug level decreased | 173 | 37.5 32.0–43.9ROR 37.5 · calibrated p 8e-5 ✓ | 32.9 EB05 29.0 · IC025 +4.7 3/3 methods agree | Lab value / disease marker | serious n=165 | not reported in cached trials |
| Toxic optic neuropathy | 49 | 34.9 25.9–47.0ROR 34.9 · calibrated p 2e-4 ✓ | 30.6 EB05 24.1 · IC025 +4.1 3/3 methods agree | Not in label — unassessed | serious n=49 · ♀ 0% (drug 54%) · 100% clinician | not reported in cached trials |
| Anticonvulsant drug level below therapeutic | 84 | 33.7 26.8–42.2ROR 33.7 · calibrated p 2e-4 ✓ | 29.8 EB05 24.8 · IC025 +4.3 3/3 methods agree | Lab value / disease marker | serious n=80 | not reported in cached trials |
| Brain malformation | 39 | 33.1 23.8–46.2ROR 33.2 · calibrated p 2e-4 ✓ | 29.2 EB05 22.3 · IC025 +3.9 3/3 methods agree | Not in label — unassessed | serious n=39 · ♀ 0% (drug 54%) · 100% clinician | not reported in cached trials |
| Developmental hip dysplasia | 90 | 32.9 26.4–40.9ROR 32.9 · calibrated p 2e-4 ✓ | 29.2 EB05 24.5 · IC025 +4.3 3/3 methods agree | Not in label — unassessed | serious n=90 · 100% clinician | not reported in cached trials |
| Trisomy 18 | 40 | 31.6 22.8–43.8ROR 31.6 · calibrated p 3e-4 ✓ | 28.0 EB05 21.5 · IC025 +3.9 3/3 methods agree | Not in label — unassessed | serious n=40 · 100% clinician | not reported in cached trials |
| Aura | 187 | 30.4 26.1–35.3ROR 30.4 · calibrated p 3e-4 ✓ | 27.3 EB05 24.2 · IC025 +4.4 3/3 methods agree | Not in label — unassessed | serious n=155 | not reported in cached trials |
| Necrosis ischaemic | 45 | 29.2 21.5–39.8ROR 29.2 · calibrated p 4e-4 ✓ | 26.2 EB05 20.4 · IC025 +3.9 3/3 methods agree | Not in label — unassessed | serious n=45 · ♀ 100% (drug 54%) | not reported in cached trials |
| Anticonvulsant drug level increased | 158 | 29.2 24.8–34.4ROR 29.3 · calibrated p 3e-4 ✓ | 26.4 EB05 23.1 · IC025 +4.3 3/3 methods agree | Lab value / disease marker | serious n=153 · 95% clinician | not reported in cached trials |
| Hyperammonaemic encephalopathy | 163 | 28.6 24.3–33.5ROR 28.6 · calibrated p 4e-4 ✓ | 25.8 EB05 22.7 · IC025 +4.3 3/3 methods agree | Not in label — unassessed | serious n=163 · 100% clinician | not reported in cached trials |
| Encephalitis autoimmune | 119 | 27.5 22.8–33.2ROR 27.6 · calibrated p 5e-4 ✓ | 25.0 EB05 21.4 · IC025 +4.2 3/3 methods agree | Not in label — unassessed | serious n=119 · 100% clinician | not reported in cached trials |
| Epilepsy | 2,782 | 27.2 26.2–28.3ROR 28.2 · calibrated p 4e-4 ✓ | 24.8 EB05 24.0 · IC025 +4.6 3/3 methods agree | Likely indication confounding term in indications; also in warnings | serious PRR 16.1 | NCT00537238: 2/255 (0.8%) on Levetiracetam Oral (serious AE) |
Trial evidence (ClinicalTrials.gov)
✓ Trial adverse-event data found on ClinicalTrials.gov
Largest completed trials with posted results that list Levetiracetam Oral as a study intervention. The right-hand column of the signal table shows whether each FAERS term was also recorded in these trials, with a real denominator (4 of 40 signal terms matched).
- NCT00537238 — Pregabalin Versus Levetiracetam In Partial Seizures (N=509, PHASE3; 62 AE terms posted; arms: Pregabalin; Levetiracetam)
- NCT01960075 — Established Status Epilepticus Treatment Trial (N=478, PHASE3; 96 AE terms posted; arms: Fosphenytoin (FOS); Valproic Acid; Levetiracetam)
Caveats: trial populations, doses and follow-up differ from the reporting population; AE terms are sponsor-coded and matched here by wording; absence from a trial list means the term was not reported above the sponsor's frequency threshold, not that it cannot occur.
Most frequently reported reactions
By raw co-report count, regardless of disproportionality. Common terms here are often the illness itself or generic outcomes.
| Reaction | Reports | PRR 95% CI · ROR · χ²/p | EBGM EB05 · IC025 | Label screen | Serious-only & strata | Trial cross-check |
|---|---|---|---|---|---|---|
| Drug ineffective (drug did not work) | 9,024 | 1.9 1.8–1.9ROR 2.0 · calibrated p 0.937 | 1.9 EB05 1.8 · IC025 +0.9 | Reporting / coding artifact | serious PRR 3.1 | not reported in cached trials |
| Seizure | 8,856 | 22.7 22.2–23.2ROR 25.5 · calibrated p 6e-4 ✓ | 21.0 EB05 20.6 · IC025 +4.4 3/3 methods agree | Likely indication confounding term in indications; also in warnings | serious PRR 13.9 | NCT00537238: 1/255 (0.4%) on Levetiracetam Oral (serious AE) |
| Off label use (used outside approved label) | 6,474 | 2.0 2.0–2.1ROR 2.1 · calibrated p 0.985 | 2.0 EB05 2.0 · IC025 +1.0 | Reporting / coding artifact | serious PRR 2.1 | not reported in cached trials |
| Maternal exposure during pregnancy | 3,114 | 9.9 9.6–10.3ROR 10.3 · calibrated p 0.029 ✓ | 9.6 EB05 9.3 · IC025 +3.2 3/3 methods agree | Reporting / coding artifact | serious PRR 7.7 · ♀ 94% (drug 54%) | not reported in cached trials |
| Epilepsy | 2,782 | 27.2 26.2–28.3ROR 28.2 · calibrated p 4e-4 ✓ | 24.8 EB05 24.0 · IC025 +4.6 3/3 methods agree | Likely indication confounding term in indications; also in warnings | serious PRR 16.1 | NCT00537238: 2/255 (0.8%) on Levetiracetam Oral (serious AE) |
| Foetal exposure during pregnancy | 2,537 | 8.7 8.4–9.1ROR 9.0 · calibrated p 0.046 ✓ | 8.5 EB05 8.2 · IC025 +3.0 3/3 methods agree | Reporting / coding artifact | serious PRR 5.6 · 91% clinician | not reported in cached trials |
| Drug interaction | 2,485 | 4.3 4.2–4.5ROR 4.4 · calibrated p 0.307 | 4.3 EB05 4.1 · IC025 +2.0 3/3 methods agree | Reporting / coding artifact | serious PRR 3.0 · 91% clinician | not reported in cached trials |
| Fatigue (tiredness) | 2,457 | 0.9 0.8–0.9ROR 0.9 · calibrated p 0.216 | 0.9 EB05 0.8 · IC025 -0.3 PRR-only: not supported by EBGM or IC | Labeled adverse reaction exact term | serious PRR 0.8 | not reported in cached trials |
| Condition aggravated | 2,291 | 2.1 2.0–2.2ROR 2.1 · calibrated p 0.999 | 2.1 EB05 2.0 · IC025 +1.0 | Reporting / coding artifact | serious PRR 1.9 | not reported in cached trials |
| Somnolence (drowsiness) | 2,091 | 2.9 2.7–3.0ROR 2.9 · calibrated p 0.659 | 2.8 EB05 2.7 · IC025 +1.4 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 2.8 | NCT00537238: 76/255 (29.8%) on Levetiracetam Oral |
| Status epilepticus | 2,084 | 61.4 58.6–64.4ROR 63.1 · calibrated p 3e-6 ✓ | 50.1 EB05 48.3 · IC025 +5.6 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 32.6 · 91% clinician | NCT00537238: 2/255 (0.8%) on Levetiracetam Oral (serious AE) |
| Generalised tonic-clonic seizure | 2,032 | 38.5 36.8–40.3ROR 39.5 · calibrated p 6e-5 ✓ | 33.8 EB05 32.6 · IC025 +5.0 3/3 methods agree | Likely indication confounding term in indications; also in warnings | serious PRR 22.2 | not reported in cached trials |
| Toxicity to various agents | 1,865 | 3.0 2.9–3.2ROR 3.1 · calibrated p 0.595 | 3.0 EB05 2.9 · IC025 +1.5 3/3 methods agree | Not in label — unassessed | serious PRR 2.0 · 97% clinician | not reported in cached trials |
| Fall | 1,841 | 1.5 1.4–1.6ROR 1.5 · calibrated p 0.657 | 1.5 EB05 1.5 · IC025 +0.5 | Labeled adverse reaction exact term | serious PRR 1.1 | NCT00537238: 1/255 (0.4%) on Levetiracetam Oral (serious AE) |
| Dizziness | 1,746 | 1.0 0.9–1.0ROR 1.0 · calibrated p 0.277 | 1.0 EB05 0.9 · IC025 -0.1 PRR-only: not supported by EBGM or IC | Labeled adverse reaction exact term | serious PRR 0.9 | NCT00537238: 1/254 (0.4%) on Levetiracetam Oral (serious AE) |
Unlabeled candidate signals
These flagged terms were not found in the FDA label text and do not match an artifact pattern. They are the pairs that would merit a structured assessment (temporality, dose-response, biological plausibility, consistency across databases, trial or cohort evidence). The screen has not done that; string-matching misses label wording, and a strong PRR can still be stimulated reporting, co-medication, or the disease itself.
- Tuberous sclerosis complex — n=49, PRR 242.9
- Postictal psychosis — n=71, PRR 231.7
- Postictal paralysis — n=47, PRR 65.5 (also seen in trial arm)
- Intensive care unit acquired weakness — n=54, PRR 44.7
- Infantile spasms — n=99, PRR 43.7
- Deja vu — n=37, PRR 42.7
- Vagal nerve stimulator implantation — n=39, PRR 41.1
- Tonic convulsion — n=177, PRR 39.2
- Propofol infusion syndrome — n=88, PRR 38.7
- Toxic optic neuropathy — n=49, PRR 34.9
✓ A hand-written Bradford Hill causality assessment exists for this drug: Minoxidil (oral) ↔ Pericardial effusion.
Want to assess one of these properly? The runbook describes the Bradford Hill / trial-evidence workflow used on the assessment page, and handoff_top1000_signals.csv lists the strongest unassessed pairs across all drugs.
Common questions
What are the most reported side effects of Levetiracetam Oral?
In FDA FAERS, the most frequently co-reported reaction terms for Levetiracetam Oral are seizure, epilepsy, fatigue, somnolence, status epilepticus, generalised tonic-clonic seizure. These are report counts, not rates: FAERS has no denominator, reporting is voluntary and uneven, and a term can be reported because of the illness being treated rather than the drug.
Does Levetiracetam Oral have an FDA boxed warning?
No. The FDA label retrieved for Levetiracetam Oral has no boxed warning; see the label's Warnings and Precautions for the recognised risks.
Do FAERS signals prove that Levetiracetam Oral causes these side effects?
No. A disproportionality signal (PRR, ROR) means a reaction is reported more often with this drug than with others in the database. That can reflect a real effect, but also the disease being treated, stimulated reporting after news or litigation, co-medications, or how reports are coded. Causality needs temporality, dose-response, biological plausibility, consistency across data sources and, ideally, trial or cohort evidence. This page screens each term against the FDA label and ClinicalTrials.gov results; it does not establish causation.
Sources & methods
- FDA label via openFDA (set ID 08e1bfea-7f3f-42d9-823d-f75080e664ff, effective 20251112; matched on
openfda.generic_name.exact:"LEVETIRACETAM") - Bayesian shrinkage measures computed offline over all 1,317,300 cached pairs: BCPNN information component (IC, with Norén closed-form IC025) and MGPS empirical-Bayes geometric mean (EBGM, EB05) with a two-component gamma prior fitted by maximum marginal likelihood (α₁=0.57, β₁=0.02, α₂=1.42, β₂=0.70, w=0.17); unstratified
- FAERS pair statistics from the OpenPV build of 2026-09-14 (openFDA
count=aggregation, fieldpatient.drug.openfda.generic_name.exact, 1,293 reaction terms, min 3 co-reports); PRR/ROR with 95% CI, chi-square with Yates correction - Serious-only and stratified counts (serious:1, patient.patientsex, primarysource.qualification) from openFDA count queries; serious-only PRR uses the drug serious report total and the term global serious total (N_serious=11,882,979); strata shown only when n ≥ 20
- Seriousness and sex counts from openFDA
count=serious,patient.patientsex,seriousnessdeath - ClinicalTrials.gov API v2 (query
LEVETIRACETAM, results-bearing studies sorted by enrollment)
Page generated 2026-10-14. Label and PubChem text are retrieved automatically and may lag the current label; always check the current prescribing information. OpenPV is a beta research tool of the Open Source Medicine Foundation.