Oxcarbazepine side effects: what 31,339 FDA adverse event reports show
Who reports
31,339 reports · 76% serious · 2,175 with death outcome · 59% female
Used for
Oxcarbazepine tablets are indicated for use as monotherapy or adjunctive therapy in the treatment of partial-onset seizures in adults and as monotherapy in the treatment of partial-onset seizures in pediatric patients aged 4 years and above, and as adjunctive therapy in pediatric patients aged 2 years and above with partial-onset seizures.
What it is
Oxcarbazepine is an AED available as 150 mg, 300 mg, and 600 mg film-coated tablets for oral administration. Oxcarbazepine is 10,11-Dihydro-10-oxo-5 H -dibenz[b, f ]azepine-5-carboxamide, and its structural formula is: Oxcarbazepine is a white to faintly orange crystalline powder.
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). 1,183 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 |
|---|---|---|---|---|---|---|
| Mitochondrial dna mutation | 33 | 405.7 262.3–627.5ROR 406.1 · calibrated p 5e-12 ✓ | 217.4 EB05 162.0 · IC025 +5.1 3/3 methods agree vs other Anti-epileptic Agents: PRR 12.4 (7.8–19.7) | Not in label — unassessed | serious n=33 · ♀ 100% (drug 59%) · 100% clinician | not reported in cached trials |
| Simple partial seizures | 232 | 258.4 221.9–300.8ROR 260.2 · calibrated p 5e-11 ✓ | 181.6 EB05 162.8 · IC025 +6.8 3/3 methods agree vs other Anti-epileptic Agents: PRR 25.3 (20.5–31.3) | Labeled (related wording) related wording | serious n=43 | not reported in cached trials |
| Focal dyscognitive seizures | 311 | 243.3 213.6–277.2ROR 245.7 · calibrated p 7e-11 ✓ | 174.6 EB05 159.0 · IC025 +6.9 3/3 methods agree vs other Anti-epileptic Agents: PRR 7.8 (6.8–9.0) | Likely indication confounding shares a disease stem with the indications wording | serious n=84 | not reported in cached trials |
| Partial seizures with secondary generalisation | 106 | 189.8 152.9–235.7ROR 190.4 · calibrated p 9e-10 ✓ | 142.9 EB05 121.5 · IC025 +6.1 3/3 methods agree vs other Anti-epileptic Agents: PRR 5.5 (4.4–6.8) | Labeled (related wording) related wording | serious n=31 · 100% clinician | not reported in cached trials |
| Csf oligoclonal band present | 20 | 126.6 78.4–204.5ROR 126.7 · calibrated p 9e-8 ✓ | 96.3 EB05 65.9 · IC025 +4.1 3/3 methods agree vs other Anti-epileptic Agents: PRR 8.4 (4.8–14.5) | Lab value / disease marker | serious n=20 | not reported in cached trials |
| Epileptic encephalopathy | 25 | 82.8 54.6–125.6ROR 82.9 · calibrated p 1e-6 ✓ | 69.7 EB05 49.6 · IC025 +4.3 3/3 methods agree vs other Anti-epileptic Agents: PRR 5.2 (3.3–8.2) | Not in label — unassessed | serious n=25 | not reported in cached trials |
| Multiple-drug resistance | 327 | 76.7 68.4–85.9ROR 77.4 · calibrated p 8e-7 ✓ | 68.3 EB05 62.3 · IC025 +5.8 3/3 methods agree vs other Anti-epileptic Agents: PRR 1.7 (1.5–1.9) | Reporting / coding artifact | serious n=237 · 92% clinician | not reported in cached trials |
| Central hypothyroidism | 32 | 74.9 52.0–108.1ROR 75.0 · calibrated p 2e-6 ✓ | 64.7 EB05 48.0 · IC025 +4.5 3/3 methods agree vs other Anti-epileptic Agents: only this drug | Not in label — unassessed | serious n=32 · 100% clinician | not reported in cached trials |
| Sudden unexplained death in epilepsy | 56 | 74.9 56.8–98.8ROR 75.0 · calibrated p 1e-6 ✓ | 65.7 EB05 52.5 · IC025 +5.0 3/3 methods agree vs other Anti-epileptic Agents: PRR 1.5 (1.2–2.0) | Not in label — unassessed | serious n=56 · ♀ 34% (drug 59%) · 100% clinician | not reported in cached trials |
| Lennox-gastaut syndrome | 23 | 73.9 48.0–113.8ROR 73.9 · calibrated p 3e-6 ✓ | 63.0 EB05 44.2 · IC025 +4.1 3/3 methods agree vs other Anti-epileptic Agents: PRR 6.2 (3.8–10.1) | Not in label — unassessed | serious n=23 | not reported in cached trials |
| Multiple drug therapy | 55 | 55.5 42.1–73.0ROR 55.5 · calibrated p 1e-5 ✓ | 50.3 EB05 40.1 · IC025 +4.7 3/3 methods agree vs other Anti-epileptic Agents: PRR 118.4 (53.9–260.0) | Reporting / coding artifact | serious n=55 · ♀ 100% (drug 59%) | not reported in cached trials |
| Psychogenic seizure | 62 | 46.7 36.1–60.4ROR 46.8 · calibrated p 3e-5 ✓ | 43.0 EB05 34.8 · IC025 +4.6 3/3 methods agree vs other Anti-epileptic Agents: PRR 12.1 (8.7–16.9) | Likely indication confounding shares a disease stem with the indications wording | serious n=58 · ♀ 83% (drug 59%) | not reported in cached trials |
| Creatinine renal clearance increased | 50 | 46.2 34.7–61.5ROR 46.3 · calibrated p 3e-5 ✓ | 42.5 EB05 33.5 · IC025 +4.5 3/3 methods agree vs other Anti-epileptic Agents: only this drug | Lab value / disease marker | serious n=50 · ♀ 100% (drug 59%) · 100% clinician | not reported in cached trials |
| Seizure cluster | 51 | 43.9 33.0–58.3ROR 43.9 · calibrated p 4e-5 ✓ | 40.6 EB05 32.0 · IC025 +4.4 3/3 methods agree vs other Anti-epileptic Agents: PRR 2.0 (1.5–2.7) | Likely indication confounding shares a disease stem with the indications wording | serious n=47 | not reported in cached trials |
| Complex partial seizures | 71 | 43.6 34.3–55.4ROR 43.7 · calibrated p 4e-5 ✓ | 40.4 EB05 33.1 · IC025 +4.6 3/3 methods agree vs other Anti-epileptic Agents: PRR 2.4 (1.8–3.0) | Labeled (related wording) related wording | serious n=66 | not reported in cached trials |
| Myoclonic epilepsy | 89 | 41.7 33.6–51.6ROR 41.8 · calibrated p 5e-5 ✓ | 38.9 EB05 32.6 · IC025 +4.7 3/3 methods agree vs other Anti-epileptic Agents: PRR 1.6 (1.3–2.0) | Not in label — unassessed | serious n=89 | not reported in cached trials |
| Infantile spasms | 42 | 40.4 29.6–55.2ROR 40.5 · calibrated p 7e-5 ✓ | 37.5 EB05 28.9 · IC025 +4.2 3/3 methods agree vs other Anti-epileptic Agents: PRR 1.7 (1.2–2.3) | Not in label — unassessed | serious n=42 · 100% clinician | not reported in cached trials |
| Petit mal epilepsy | 296 | 40.1 35.6–45.0ROR 40.4 · calibrated p 5e-5 ✓ | 37.7 EB05 34.2 · IC025 +5.0 3/3 methods agree vs other Anti-epileptic Agents: PRR 2.2 (1.9–2.4) | Labeled (related wording) related wording | serious n=281 | not reported in cached trials |
| Propofol infusion syndrome | 40 | 38.9 28.3–53.5ROR 39.0 · calibrated p 9e-5 ✓ | 36.2 EB05 27.7 · IC025 +4.1 3/3 methods agree vs other Anti-epileptic Agents: PRR 5.7 (4.0–8.2) | Not in label — unassessed | serious n=40 · ♀ 100% (drug 59%) · 100% clinician | not reported in cached trials |
| Partial seizures | 288 | 38.3 34.1–43.2ROR 38.7 · calibrated p 7e-5 ✓ | 36.1 EB05 32.8 · IC025 +4.9 3/3 methods agree vs other Anti-epileptic Agents: PRR 2.3 (2.0–2.6) | Likely indication confounding term in indications; also in warnings | serious n=275 | not reported in cached trials |
| Blood gases abnormal | 29 | 37.2 25.6–54.0ROR 37.2 · calibrated p 1e-4 ✓ | 34.4 EB05 25.2 · IC025 +3.9 3/3 methods agree vs other Anti-epileptic Agents: PRR 15.1 (9.0–25.2) | Lab value / disease marker | serious n=28 · ♀ 100% (drug 59%) · 100% clinician | not reported in cached trials |
| Atonic seizures | 42 | 36.0 26.4–49.2ROR 36.1 · calibrated p 1e-4 ✓ | 33.7 EB05 26.0 · IC025 +4.1 3/3 methods agree vs other Anti-epileptic Agents: PRR 1.4 (1.0–1.9) | Likely indication confounding shares a disease stem with the indications wording | serious n=39 | not reported in cached trials |
| Change in seizure presentation | 33 | 34.3 24.2–48.7ROR 34.3 · calibrated p 2e-4 ✓ | 32.1 EB05 23.9 · IC025 +3.9 3/3 methods agree vs other Anti-epileptic Agents: PRR 1.5 (1.1–2.2) | Likely indication confounding shares a disease stem with the indications wording | serious n=31 · 100% clinician | not reported in cached trials |
| Temporal lobe epilepsy | 21 | 32.4 20.9–50.3ROR 32.4 · calibrated p 3e-4 ✓ | 30.2 EB05 20.8 · IC025 +3.5 3/3 methods agree vs other Anti-epileptic Agents: PRR 12.7 (7.1–22.6) | Not in label — unassessed | serious n=20 | not reported in cached trials |
| Sedation complication | 108 | 29.3 24.1–35.5ROR 29.3 · calibrated p 3e-4 ✓ | 27.9 EB05 23.8 · IC025 +4.3 3/3 methods agree vs other Anti-epileptic Agents: PRR 31.9 (22.9–44.5) | Reporting / coding artifact | serious n=106 · ♀ 100% (drug 59%) · 93% clinician | not reported in cached trials |
| Aura | 78 | 28.4 22.6–35.6ROR 28.4 · calibrated p 4e-4 ✓ | 27.0 EB05 22.4 · IC025 +4.2 3/3 methods agree vs other Anti-epileptic Agents: PRR 2.0 (1.6–2.6) | Labeled adverse reaction exact term | serious n=53 | not reported in cached trials |
| Hypochloraemia | 46 | 26.6 19.8–35.7ROR 26.6 · calibrated p 6e-4 ✓ | 25.4 EB05 19.8 · IC025 +3.8 3/3 methods agree vs other Anti-epileptic Agents: only this drug | Not in label — unassessed | serious n=45 · 100% clinician | not reported in cached trials |
| Trigeminal neuralgia | 158 | 26.5 22.6–31.0ROR 26.6 · calibrated p 5e-4 ✓ | 25.4 EB05 22.2 · IC025 +4.3 3/3 methods agree vs other Anti-epileptic Agents: PRR 95.2 (62.5–145.2) | Not in label — unassessed | serious n=121 | not reported in cached trials |
| Tonic convulsion | 55 | 26.5 20.2–34.6ROR 26.5 · calibrated p 6e-4 ✓ | 25.3 EB05 20.1 · IC025 +3.9 3/3 methods agree vs other Anti-epileptic Agents: PRR 1.4 (1.1–1.9) | Not in label — unassessed | serious n=55 · 100% clinician | not reported in cached trials |
| Anticonvulsant drug level decreased | 54 | 25.5 19.4–33.4ROR 25.5 · calibrated p 8e-4 ✓ | 24.4 EB05 19.4 · IC025 +3.9 3/3 methods agree vs other Anti-epileptic Agents: PRR 1.1 (0.8–1.4) | Lab value / disease marker | serious n=52 | not reported in cached trials |
| Pleocytosis | 21 | 24.4 15.8–37.7ROR 24.4 · calibrated p 0.001 ✓ | 23.1 EB05 15.9 · IC025 +3.2 3/3 methods agree vs other Anti-epileptic Agents: PRR 5.8 (3.5–9.5) | Not in label — unassessed | serious n=21 · ♀ 100% (drug 59%) | not reported in cached trials |
| Hyperammonaemic encephalopathy | 62 | 24.3 18.9–31.3ROR 24.4 · calibrated p 9e-4 ✓ | 23.3 EB05 18.8 · IC025 +3.9 3/3 methods agree vs other Anti-epileptic Agents: PRR 1.6 (1.2–2.1) | Not in label — unassessed | serious n=62 · 100% clinician | not reported in cached trials |
| Electroencephalogram abnormal | 113 | 24.1 19.9–29.0ROR 24.1 · calibrated p 9e-4 ✓ | 23.1 EB05 19.8 · IC025 +4.1 3/3 methods agree vs other Anti-epileptic Agents: PRR 2.0 (1.7–2.5) | Lab value / disease marker | serious n=107 | not reported in cached trials |
| Drug withdrawal convulsions | 62 | 23.3 18.1–30.0ROR 23.4 · calibrated p 0.001 ✓ | 22.4 EB05 18.1 · IC025 +3.8 3/3 methods agree vs other Anti-epileptic Agents: PRR 1.1 (0.9–1.5) | Labeled (related wording) related wording | serious n=56 | not reported in cached trials |
| Anticonvulsant drug level below therapeutic | 24 | 21.1 14.0–31.6ROR 21.1 · calibrated p 0.002 ✓ | 20.1 EB05 14.1 · IC025 +3.2 3/3 methods agree vs other Anti-epileptic Agents: PRR 1.1 (0.7–1.7) | Lab value / disease marker | serious n=23 | not reported in cached trials |
| Epilepsy | 931 | 20.4 19.1–21.7ROR 21.0 · calibrated p 0.002 ✓ | 19.8 EB05 18.7 · IC025 +4.2 3/3 methods agree vs other Anti-epileptic Agents: PRR 1.5 (1.4–1.6) | Labeled adverse reaction exact term | serious PRR 15.4 | NCT00908349: 2/214 (0.9%) on Oxcarbazepine (serious AE) |
| Status epilepticus | 332 | 19.6 17.6–21.8ROR 19.8 · calibrated p 0.002 ✓ | 19.0 EB05 17.4 · IC025 +4.0 3/3 methods agree vs other Anti-epileptic Agents: PRR 1.0 (0.9–1.2) | Labeled adverse reaction exact term | serious PRR 14.8 | NCT01498822: 1/174 (0.6%) on Oxcarbazepine (serious AE) |
| Congenital hydronephrosis | 20 | 18.6 11.9–28.9ROR 18.6 · calibrated p 0.004 ✓ | 17.6 EB05 11.8 · IC025 +2.9 3/3 methods agree vs other Anti-epileptic Agents: PRR 100.5 (29.9–338.1) | Not in label — unassessed | serious n=20 · 100% clinician | not reported in cached trials |
| Cryptorchism | 31 | 18.4 12.9–26.3ROR 18.4 · calibrated p 0.004 ✓ | 17.7 EB05 13.0 · IC025 +3.2 3/3 methods agree vs other Anti-epileptic Agents: PRR 7.3 (4.8–11.2) | Not in label — unassessed | serious n=31 · 100% clinician | not reported in cached trials |
| Creatinine renal clearance decreased | 104 | 17.2 14.1–20.9ROR 17.2 · calibrated p 0.004 ✓ | 16.7 EB05 14.2 · IC025 +3.6 3/3 methods agree vs other Anti-epileptic Agents: only this drug | Lab value / disease marker | serious n=104 · ♀ 100% (drug 59%) · 93% clinician | not reported in cached trials |
Trial evidence (ClinicalTrials.gov)
✓ Trial adverse-event data found on ClinicalTrials.gov
Largest completed trials with posted results that list Oxcarbazepine 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 (2 of 40 signal terms matched).
- NCT01498822 — Levetiracetam Versus Oxcarbazepine as Monotherapy to Evaluate Efficacy and Safety in Subjects With Newly or Re (N=353, PHASE4; 28 AE terms posted; arms: Levetiracetam; Oxcarbazepine)
- NCT00908349 — Safety and Tolerability of OXC XR as Adjunctive Therapy in Subjects With Refractory Partial Epilepsy (N=214, PHASE3; 23 AE terms posted; arms: Oxcarbazepine XR)
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) | 2,981 | 1.5 1.4–1.5ROR 1.5 · calibrated p 0.653 | 1.5 EB05 1.4 · IC025 +0.5 vs other Anti-epileptic Agents: PRR 1.3 (1.3–1.4) | Reporting / coding artifact | serious PRR 2.4 | not reported in cached trials |
| Seizure | 2,923 | 16.9 16.4–17.5ROR 18.5 · calibrated p 0.003 ✓ | 16.5 EB05 16.0 · IC025 +4.0 3/3 methods agree vs other Anti-epileptic Agents: PRR 1.8 (1.7–1.9) | Likely indication confounding term in indications; also in warnings | serious PRR 12.2 | not reported in cached trials |
| Off label use (used outside approved label) | 1,751 | 1.3 1.3–1.4ROR 1.3 · calibrated p 0.527 | 1.3 EB05 1.3 · IC025 +0.3 vs other Anti-epileptic Agents: PRR 1.4 (1.4–1.5) | Reporting / coding artifact | serious PRR 1.4 | not reported in cached trials |
| Fatigue (tiredness) | 1,641 | 1.4 1.3–1.4ROR 1.4 · calibrated p 0.570 | 1.4 EB05 1.3 · IC025 +0.4 vs other Anti-epileptic Agents: PRR 1.7 (1.6–1.7) | Labeled adverse reaction exact term | serious PRR 1.2 | not reported in cached trials |
| Dizziness | 1,558 | 2.0 1.9–2.1ROR 2.1 · calibrated p 0.990 | 2.0 EB05 1.9 · IC025 +0.9 vs other Anti-epileptic Agents: PRR 1.6 (1.6–1.7) | Labeled adverse reaction exact term | serious PRR 2.1 | NCT01498822: 1/173 (0.6%) on Oxcarbazepine (serious AE) |
| Convulsion (seizure) | 1,464 | 16.8 15.9–17.7ROR 17.5 · calibrated p 0.004 ✓ | 16.4 EB05 15.7 · IC025 +3.9 3/3 methods agree vs other Anti-epileptic Agents: PRR 2.2 (2.1–2.3) | Labeled adverse reaction exact term | serious PRR 12.4 | NCT01498822: 5/174 (2.9%) on Oxcarbazepine (serious AE) |
| Headache | 1,462 | 1.5 1.4–1.6ROR 1.5 · calibrated p 0.668 | 1.5 EB05 1.5 · IC025 +0.5 vs other Anti-epileptic Agents: PRR 1.7 (1.6–1.8) | Labeled adverse reaction exact term | serious PRR 1.5 | NCT01498822: 36/174 (20.7%) on Oxcarbazepine |
| Somnolence (drowsiness) | 1,462 | 4.7 4.5–5.0ROR 4.9 · calibrated p 0.243 | 4.7 EB05 4.5 · IC025 +2.2 3/3 methods agree vs other Anti-epileptic Agents: PRR 1.6 (1.5–1.7) | Labeled adverse reaction exact term | serious PRR 4.1 | NCT01498822: 24/174 (13.8%) on Oxcarbazepine |
| Nausea | 1,340 | 1.1 1.0–1.2ROR 1.1 · calibrated p 0.377 | 1.1 EB05 1.1 · IC025 +0.0 vs other Anti-epileptic Agents: PRR 1.4 (1.3–1.5) | Labeled adverse reaction exact term | serious PRR 1.1 | NCT00908349: 16/214 (7.5%) on Oxcarbazepine |
| Hyponatraemia (low sodium) | 1,305 | 15.4 14.6–16.3ROR 16.0 · calibrated p 0.005 ✓ | 15.1 EB05 14.4 · IC025 +3.8 3/3 methods agree vs other Anti-epileptic Agents: PRR 8.2 (7.6–8.7) | Labeled adverse reaction exact term | serious PRR 10.2 | NCT01498822: 1/174 (0.6%) on Oxcarbazepine (serious AE) |
| Fall | 1,220 | 2.4 2.3–2.5ROR 2.4 · calibrated p 0.839 | 2.4 EB05 2.3 · IC025 +1.2 3/3 methods agree vs other Anti-epileptic Agents: PRR 1.8 (1.7–1.9) | Labeled adverse reaction exact term | serious PRR 1.9 | not reported in cached trials |
| Vomiting | 1,147 | 1.6 1.5–1.7ROR 1.6 · calibrated p 0.713 | 1.6 EB05 1.5 · IC025 +0.6 vs other Anti-epileptic Agents: PRR 1.5 (1.4–1.5) | Labeled adverse reaction exact term | serious PRR 1.5 | NCT00908349: 13/214 (6.1%) on Oxcarbazepine |
| Drug interaction | 1,054 | 4.3 4.1–4.6ROR 4.4 · calibrated p 0.305 | 4.3 EB05 4.1 · IC025 +2.0 3/3 methods agree vs other Anti-epileptic Agents: PRR 0.9 (0.9–1.0) | Reporting / coding artifact | serious PRR 3.3 | not reported in cached trials |
| Rash | 1,012 | 1.5 1.4–1.6ROR 1.5 · calibrated p 0.663 | 1.5 EB05 1.4 · IC025 +0.5 vs other Anti-epileptic Agents: PRR 0.9 (0.9–1.0) | Labeled adverse reaction exact term | serious PRR 1.8 | NCT01498822: 13/174 (7.5%) on Oxcarbazepine |
| Anxiety | 991 | 2.3 2.1–2.4ROR 2.3 · calibrated p 0.904 | 2.3 EB05 2.1 · IC025 +1.1 3/3 methods agree vs other Anti-epileptic Agents: PRR 1.5 (1.4–1.6) | Labeled adverse reaction exact term | serious PRR 1.7 | not reported in cached trials |
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.
- Mitochondrial dna mutation — n=33, PRR 405.7
- Epileptic encephalopathy — n=25, PRR 82.8
- Central hypothyroidism — n=32, PRR 74.9
- Sudden unexplained death in epilepsy — n=56, PRR 74.9
- Lennox-gastaut syndrome — n=23, PRR 73.9
- Myoclonic epilepsy — n=89, PRR 41.7
- Infantile spasms — n=42, PRR 40.4
- Propofol infusion syndrome — n=40, PRR 38.9
- Temporal lobe epilepsy — n=21, PRR 32.4
- Hypochloraemia — n=46, PRR 26.6
✓ A hand-written Bradford Hill causality assessment exists for this drug: Oxcarbazepine ↔ Hyponatraemia.
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 Oxcarbazepine?
In FDA FAERS, the most frequently co-reported reaction terms for Oxcarbazepine are seizure, fatigue, dizziness, convulsion, headache, somnolence. 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 Oxcarbazepine have an FDA boxed warning?
No. The FDA label retrieved for Oxcarbazepine has no boxed warning; see the label's Warnings and Precautions for the recognised risks.
Do FAERS signals prove that Oxcarbazepine 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 1176d5f5-3447-4925-aed8-1a1cb4b5989d, effective 20251013; matched on
openfda.generic_name.exact:"OXCARBAZEPINE") - 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, 1,223 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
OXCARBAZEPINE, 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.