Divalproex side effects: what 46,254 FDA adverse event reports show
Drug class
Anti-epileptic drug
Label matched
Divalproex Sodium (Divalproex Sodium)
Who reports
46,254 reports · 67% serious · 2,570 with death outcome · 52% female
Used for
Divalproex sodium is an anti-epileptic drug indicated for: Treatment of manic episodes associated with bipolar disorder (1.1) Monotherapy and adjunctive therapy of complex partial seizures and simple and complex absence seizures; adjunctive therapy in .
What it is
Divalproex sodium is a stable co-ordination compound comprised of sodium valproate and valproic acid in a 1:1 molar relationship.
Boxed warning
LIFE THREATENING ADVERSE REACTIONS Hepatotoxicity General Population: Hepatic failure resulting in fatalities has occurred in patients receiving valproate and its derivatives. These incidents usually have occurred during the first six months of treatment.
Causality screen of the 40 strongest signals
What the badges mean
- Labeled — boxed warning The term (or its clinical synonym) appears in the FDA boxed warning: causality is regulator-recognised and considered serious.
- 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). 1,189 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 |
|---|---|---|---|---|---|---|
| Neural tube defect | 324 | 370.7 320.0–429.5ROR 373.4 · calibrated p 1e-12 ✓ | 200.6 EB05 182.9 · IC025 +7.1 3/3 methods agree | Labeled — boxed warning exact term | serious n=327 · 100% consumer | no trial arm names this drug |
| Life expectancy shortened | 196 | 237.0 199.4–281.8ROR 238.0 · calibrated p 1e-10 ✓ | 152.9 EB05 135.7 · IC025 +6.6 3/3 methods agree | Not in label — unassessed | serious n=196 · 100% consumer | no trial arm names this drug |
| Total lung capacity increased | 89 | 219.4 170.3–282.8ROR 219.9 · calibrated p 3e-10 ✓ | 143.0 EB05 119.7 · IC025 +6.0 3/3 methods agree | Not in label — unassessed | serious n=89 · ♀ 100% (drug 52%) · 100% clinician | no trial arm names this drug |
| Congenital cardiovascular anomaly | 188 | 128.9 109.6–151.5ROR 129.4 · calibrated p 2e-8 ✓ | 99.2 EB05 87.9 · IC025 +6.1 3/3 methods agree | Labeled (related wording) related wording | serious n=188 · 100% consumer | no trial arm names this drug |
| Spina bifida | 428 | 115.8 104.2–128.8ROR 116.9 · calibrated p 4e-8 ✓ | 91.8 EB05 84.7 · IC025 +6.2 3/3 methods agree | Labeled — boxed warning exact term | serious n=431 · 81% consumer | no trial arm names this drug |
| Neovascularisation | 50 | 109.9 80.7–149.8ROR 110.0 · calibrated p 1e-7 ✓ | 85.6 EB05 67.5 · IC025 +5.1 3/3 methods agree | Not in label — unassessed | serious n=50 · ♀ 100% (drug 52%) · 100% clinician | no trial arm names this drug |
| Asthma-chronic obstructive pulmonary disease overlap syndrome | 89 | 93.5 74.4–117.4ROR 93.6 · calibrated p 3e-7 ✓ | 76.2 EB05 63.8 · IC025 +5.4 3/3 methods agree | Not in label — unassessed | serious n=89 · ♀ 100% (drug 52%) · 100% clinician | no trial arm names this drug |
| Schizoaffective disorder | 249 | 73.1 63.9–83.5ROR 73.4 · calibrated p 1e-6 ✓ | 62.6 EB05 56.4 · IC025 +5.6 3/3 methods agree | Not in label — unassessed | serious n=244 | no trial arm names this drug |
| Physical disability | 543 | 62.9 57.5–68.8ROR 63.6 · calibrated p 3e-6 ✓ | 55.1 EB05 51.3 · IC025 +5.6 3/3 methods agree | Labeled (related wording) related wording | serious n=542 · 100% consumer | no trial arm names this drug |
| Loss of employment | 345 | 57.8 51.7–64.7ROR 58.2 · calibrated p 5e-6 ✓ | 51.2 EB05 46.8 · IC025 +5.4 3/3 methods agree | Not in label — unassessed | serious n=341 · 81% consumer | no trial arm names this drug |
| Sinus rhythm | 42 | 47.9 34.9–65.9ROR 48.0 · calibrated p 3e-5 ✓ | 42.6 EB05 32.8 · IC025 +4.3 3/3 methods agree | Not in label — unassessed | serious n=42 · ♀ 100% (drug 52%) · 100% clinician | no trial arm names this drug |
| Medication residue | 209 | 39.3 34.1–45.3ROR 39.5 · calibrated p 6e-5 ✓ | 36.1 EB05 32.2 · IC025 +4.8 3/3 methods agree | Labeled adverse reaction exact term | – | no trial arm names this drug |
| Congenital musculoskeletal anomaly | 34 | 37.4 26.3–53.0ROR 37.4 · calibrated p 1e-4 ✓ | 34.0 EB05 25.4 · IC025 +4.0 3/3 methods agree | Labeled (related wording) related wording | serious n=34 | no trial arm names this drug |
| Multiple congenital abnormalities | 110 | 37.0 30.5–45.0ROR 37.1 · calibrated p 9e-5 ✓ | 34.1 EB05 29.1 · IC025 +4.6 3/3 methods agree | Labeled (related wording) related wording | serious n=112 · 100% consumer | no trial arm names this drug |
| Social problem | 311 | 36.7 32.7–41.2ROR 37.0 · calibrated p 9e-5 ✓ | 34.0 EB05 30.9 · IC025 +4.8 3/3 methods agree | Reporting / coding artifact | serious n=308 · 100% consumer | no trial arm names this drug |
| Foetal anticonvulsant syndrome | 83 | 33.6 26.9–42.0ROR 33.7 · calibrated p 2e-4 ✓ | 31.2 EB05 25.9 · IC025 +4.4 3/3 methods agree | Labeled (related wording) related wording | serious n=83 · 100% clinician | no trial arm names this drug |
| Anticonvulsant drug level below therapeutic | 51 | 32.5 24.4–43.1ROR 32.5 · calibrated p 2e-4 ✓ | 30.0 EB05 23.7 · IC025 +4.1 3/3 methods agree | Lab value / disease marker | serious n=38 | no trial arm names this drug |
| Hyperammonaemia | 327 | 31.7 28.3–35.5ROR 31.9 · calibrated p 2e-4 ✓ | 29.6 EB05 27.0 · IC025 +4.6 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=289 · 93% clinician | no trial arm names this drug |
| Atonic seizures | 52 | 31.6 23.8–41.8ROR 31.6 · calibrated p 3e-4 ✓ | 29.3 EB05 23.2 · IC025 +4.1 3/3 methods agree | Labeled (related wording) related wording | serious n=47 · ♀ 0% (drug 52%) · 73% consumer | no trial arm names this drug |
| Anticonvulsant drug level decreased | 93 | 31.5 25.6–38.9ROR 31.6 · calibrated p 2e-4 ✓ | 29.4 EB05 24.7 · IC025 +4.3 3/3 methods agree | Lab value / disease marker | serious n=75 | no trial arm names this drug |
| Granulocytopenia | 371 | 31.3 28.1–34.7ROR 31.5 · calibrated p 2e-4 ✓ | 29.2 EB05 26.8 · IC025 +4.6 3/3 methods agree | Not in label — unassessed | serious n=346 · 100% clinician | no trial arm names this drug |
| Ammonia increased | 322 | 30.5 27.2–34.1ROR 30.7 · calibrated p 2e-4 ✓ | 28.6 EB05 26.0 · IC025 +4.6 3/3 methods agree | Lab value / disease marker | serious n=202 | no trial arm names this drug |
| Anticonvulsant drug level increased | 99 | 29.3 23.9–35.9ROR 29.4 · calibrated p 3e-4 ✓ | 27.4 EB05 23.2 · IC025 +4.3 3/3 methods agree | Lab value / disease marker | serious n=77 | no trial arm names this drug |
| Diabetic coma | 170 | 28.9 24.8–33.8ROR 29.0 · calibrated p 3e-4 ✓ | 27.2 EB05 23.9 · IC025 +4.4 3/3 methods agree | Not in label — unassessed | serious n=170 | no trial arm names this drug |
| Deformity | 563 | 28.9 26.6–31.5ROR 29.3 · calibrated p 3e-4 ✓ | 27.2 EB05 25.4 · IC025 +4.6 3/3 methods agree | Not in label — unassessed | serious PRR 26.7 · 90% consumer | no trial arm names this drug |
| Hypomania | 217 | 28.3 24.7–32.4ROR 28.4 · calibrated p 4e-4 ✓ | 26.6 EB05 23.8 · IC025 +4.4 3/3 methods agree | Not in label — unassessed | serious n=189 · ♀ 78% (drug 52%) | no trial arm names this drug |
| Diabetes mellitus non-insulin-dependent | 82 | 26.7 21.3–33.3ROR 26.7 · calibrated p 6e-4 ✓ | 25.1 EB05 20.9 · IC025 +4.1 3/3 methods agree | Not in label — unassessed | serious n=76 | no trial arm names this drug |
| Motor developmental delay | 32 | 26.6 18.6–38.0ROR 26.6 · calibrated p 7e-4 ✓ | 24.8 EB05 18.4 · IC025 +3.6 3/3 methods agree | Likely indication confounding term in indications; also in warnings | serious n=32 | no trial arm names this drug |
| Tension | 327 | 25.6 22.9–28.6ROR 25.8 · calibrated p 6e-4 ✓ | 24.3 EB05 22.1 · IC025 +4.4 3/3 methods agree | Labeled adverse reaction exact term | serious n=321 · 100% consumer | no trial arm names this drug |
| Autism | 55 | 25.5 19.5–33.5ROR 25.6 · calibrated p 7e-4 ✓ | 24.0 EB05 19.2 · IC025 +3.9 3/3 methods agree | Labeled adverse reaction exact term | serious n=53 · ♀ 0% (drug 52%) | no trial arm names this drug |
| Bipolar i disorder | 116 | 25.3 21.0–30.5ROR 25.4 · calibrated p 7e-4 ✓ | 23.9 EB05 20.5 · IC025 +4.1 3/3 methods agree | Likely indication confounding term in indications; also in warnings | serious n=102 | no trial arm names this drug |
| Hyperammonaemic encephalopathy | 86 | 23.9 19.3–29.7ROR 24.0 · calibrated p 1e-3 ✓ | 22.6 EB05 18.9 · IC025 +4.0 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=86 · 100% clinician | no trial arm names this drug |
| Cogwheel rigidity | 52 | 23.5 17.8–31.0ROR 23.5 · calibrated p 0.001 ✓ | 22.2 EB05 17.6 · IC025 +3.8 3/3 methods agree | Not in label — unassessed | serious n=49 · ♀ 29% (drug 52%) · 100% clinician | no trial arm names this drug |
| Bipolar disorder | 522 | 22.7 20.8–24.7ROR 22.9 · calibrated p 0.001 ✓ | 21.6 EB05 20.1 · IC025 +4.3 3/3 methods agree | Labeled — boxed warning exact term | serious PRR 19.2 | no trial arm names this drug |
| Seizure cluster | 38 | 22.4 16.2–31.1ROR 22.4 · calibrated p 0.002 ✓ | 21.2 EB05 16.1 · IC025 +3.5 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=34 | no trial arm names this drug |
| Complex partial seizures | 50 | 21.0 15.8–27.9ROR 21.0 · calibrated p 0.002 ✓ | 20.0 EB05 15.7 · IC025 +3.6 3/3 methods agree | Likely indication confounding term in indications; also in warnings | serious n=46 | no trial arm names this drug |
| Compulsive sexual behaviour | 35 | 20.2 14.4–28.4ROR 20.2 · calibrated p 0.002 ✓ | 19.2 EB05 14.4 · IC025 +3.4 3/3 methods agree | Not in label — unassessed | serious n=33 | no trial arm names this drug |
| Congenital anomaly | 324 | 19.6 17.6–21.9ROR 19.7 · calibrated p 0.002 ✓ | 18.8 EB05 17.2 · IC025 +4.0 3/3 methods agree | Labeled — boxed warning synonym match | serious PRR 16.3 · 72% consumer | no trial arm names this drug |
| Mania | 667 | 19.1 17.7–20.7ROR 19.4 · calibrated p 0.002 ✓ | 18.4 EB05 17.2 · IC025 +4.1 3/3 methods agree | Likely indication confounding term in indications; also in warnings | serious PRR 15.4 | no trial arm names this drug |
| Drug level fluctuating | 35 | 18.8 13.4–26.3ROR 18.8 · calibrated p 0.003 ✓ | 17.8 EB05 13.3 · IC025 +3.3 3/3 methods agree | Reporting / coding artifact | 100% clinician | no trial arm names this drug |
Trial evidence (ClinicalTrials.gov)
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) | 3,044 | 1.0 1.0–1.1ROR 1.1 · calibrated p 0.340 | 1.0 EB05 1.0 · IC025 +0.0 | Reporting / coding artifact | serious PRR 1.5 | no trial arm names this drug |
| Seizure | 2,620 | 10.6 10.2–11.0ROR 11.1 · calibrated p 0.022 ✓ | 10.3 EB05 10.0 · IC025 +3.3 3/3 methods agree | Labeled — boxed warning exact term | serious PRR 8.5 | no trial arm names this drug |
| Weight increased (weight gain) | 2,169 | 4.4 4.3–4.6ROR 4.6 · calibrated p 0.281 | 4.4 EB05 4.3 · IC025 +2.1 3/3 methods agree | Labeled (related wording) related wording | serious PRR 4.6 | no trial arm names this drug |
| Nausea | 2,109 | 1.2 1.2–1.3ROR 1.2 · calibrated p 0.455 | 1.2 EB05 1.2 · IC025 +0.2 | Labeled adverse reaction exact term | serious PRR 1.4 | no trial arm names this drug |
| Off label use (used outside approved label) | 2,082 | 1.1 1.0–1.1ROR 1.1 · calibrated p 0.367 | 1.1 EB05 1.0 · IC025 +0.0 | Reporting / coding artifact | serious PRR 1.2 | no trial arm names this drug |
| Fatigue (tiredness) | 1,963 | 1.1 1.1–1.2ROR 1.2 · calibrated p 0.408 | 1.1 EB05 1.1 · IC025 +0.1 | Labeled (related wording) related wording | serious PRR 1.1 | no trial arm names this drug |
| Somnolence (drowsiness) | 1,900 | 4.3 4.1–4.5ROR 4.5 · calibrated p 0.303 | 4.3 EB05 4.1 · IC025 +2.0 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 4.0 | no trial arm names this drug |
| Pain | 1,898 | 1.4 1.3–1.5ROR 1.4 · calibrated p 0.586 | 1.4 EB05 1.3 · IC025 +0.4 | Labeled adverse reaction exact term | serious PRR 1.6 | no trial arm names this drug |
| Tremor (shaking) | 1,824 | 5.0 4.8–5.2ROR 5.2 · calibrated p 0.216 | 5.0 EB05 4.8 · IC025 +2.2 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 4.4 | no trial arm names this drug |
| Fall | 1,776 | 2.4 2.3–2.5ROR 2.5 · calibrated p 0.819 | 2.4 EB05 2.3 · IC025 +1.2 3/3 methods agree | Not in label — unassessed | serious PRR 2.2 | no trial arm names this drug |
| Anxiety | 1,715 | 2.7 2.6–2.9ROR 2.8 · calibrated p 0.694 | 2.7 EB05 2.6 · IC025 +1.4 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 2.7 | no trial arm names this drug |
| Vomiting | 1,641 | 1.6 1.5–1.7ROR 1.6 · calibrated p 0.713 | 1.6 EB05 1.5 · IC025 +0.6 | Labeled — boxed warning exact term | serious PRR 1.6 | no trial arm names this drug |
| Headache | 1,599 | 1.2 1.1–1.2ROR 1.2 · calibrated p 0.415 | 1.2 EB05 1.1 · IC025 +0.1 | Labeled — boxed warning exact term | serious PRR 1.3 | no trial arm names this drug |
| Convulsion (seizure) | 1,562 | 12.5 11.9–13.2ROR 12.9 · calibrated p 0.013 ✓ | 12.2 EB05 11.7 · IC025 +3.5 3/3 methods agree | Labeled — boxed warning synonym match | serious PRR 9.8 | no trial arm names this drug |
| Depression | 1,559 | 3.1 3.0–3.3ROR 3.2 · calibrated p 0.571 | 3.1 EB05 3.0 · IC025 +1.5 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 2.9 | no trial arm names this drug |
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.
- Life expectancy shortened — n=196, PRR 237.0
- Total lung capacity increased — n=89, PRR 219.4
- Neovascularisation — n=50, PRR 109.9
- Asthma-chronic obstructive pulmonary disease overlap syndrome — n=89, PRR 93.5
- Schizoaffective disorder — n=249, PRR 73.1
- Loss of employment — n=345, PRR 57.8
- Sinus rhythm — n=42, PRR 47.9
- Granulocytopenia — n=371, PRR 31.3
- Diabetic coma — n=170, PRR 28.9
- Deformity — n=563, PRR 28.9
✓ A hand-written Bradford Hill causality assessment exists for this drug: Methotrexate Sodium ↔ Rheumatoid Arthritis.
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 Divalproex?
In FDA FAERS, the most frequently co-reported reaction terms for Divalproex are seizure, weight increased, nausea, fatigue, somnolence, pain. 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 Divalproex have an FDA boxed warning?
Yes. The current FDA label carries a boxed warning: LIFE THREATENING ADVERSE REACTIONS Hepatotoxicity General Population: Hepatic failure resulting in fatalities has occurred in patients receiving valproate and its derivatives. These incidents usually have occurred during the first six months of treatment.
Do FAERS signals prove that Divalproex 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 0339e27d-3dbf-4c37-a14e-f53557c08e19, effective 20260723; matched on
openfda.generic_name.exact:"DIVALPROEX SODIUM") - 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, 1,229 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
DIVALPROEX, 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.