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Drug · FAERS side-effect profile with label screen

Divalproex side effects: what 46,254 FDA adverse event reports show

Divalproex Sodium · 1,229 reaction terms · 187,908 drug–reaction co-reports · data 2026-09-14
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Drug class

Anti-epileptic drug

FDA label, Indications wording of the closest related product

Label matched

Divalproex Sodium (Divalproex Sodium)

closest FDA label found for this product string; brand list suppressed because the label is a related product, not an exact match

Who reports

46,254 reports · 67% serious · 2,570 with death outcome · 52% female

openFDA FAERS counts, all years, deduplication not applied

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 .

FDA label, Indications and Usage

What it is

Divalproex sodium is a stable co-ordination compound comprised of sodium valproate and valproic acid in a 1:1 molar relationship.

FDA label, Description section

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.

FDA label
How to read this page. FAERS is a spontaneous-reporting system: counts are not incidence rates and a signal is not proof of causation. Each reaction below is run through an automated screen — is the term in the FDA label (known), in the indications (the disease being treated), an administrative/coding term, or none of these (unlabeled)? That screen is mechanical text matching, not a causality assessment. The 30 hand-written Bradford Hill assessments are on the causality assessment page. Not medical advice.

Causality screen of the 40 strongest signals

Labeled — boxed warning 4Labeled adverse reaction 3Labeled (related wording) 6Likely indication confounding 7Reporting / coding artifact 2Lab value / disease marker 4Not in label — unassessed 14
What the badges mean

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.

Show:
ReactionReportsPRR 95% CI · ROR · χ²/pEBGM EB05 · IC025Label screenSerious-only & strataTrial cross-check
Neural tube defect324370.7
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% consumerno trial arm names this drug
Life expectancy shortened196237.0
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 — unassessedserious n=196 · 100% consumerno trial arm names this drug
Total lung capacity increased89219.4
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 — unassessedserious n=89 · ♀ 100% (drug 52%) · 100% clinicianno trial arm names this drug
Spina bifida428115.8
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% consumerno trial arm names this drug
Neovascularisation50109.9
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 — unassessedserious n=50 · ♀ 100% (drug 52%) · 100% clinicianno trial arm names this drug
Asthma-chronic obstructive pulmonary disease overlap syndrome8993.5
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 — unassessedserious n=89 · ♀ 100% (drug 52%) · 100% clinicianno trial arm names this drug
Schizoaffective disorder24973.1
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 — unassessedserious n=244no trial arm names this drug
Loss of employment34557.8
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 — unassessedserious n=341 · 81% consumerno trial arm names this drug
Sinus rhythm4247.9
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 — unassessedserious n=42 · ♀ 100% (drug 52%) · 100% clinicianno trial arm names this drug
Medication residue20939.3
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
Social problem31136.7
32.7–41.2ROR 37.0 · calibrated p 9e-5 ✓
34.0 EB05 30.9 · IC025 +4.8
3/3 methods agree
Reporting / coding artifactserious n=308 · 100% consumerno trial arm names this drug
Anticonvulsant drug level below therapeutic5132.5
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 markerserious n=38no trial arm names this drug
Hyperammonaemia32731.7
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% clinicianno trial arm names this drug
Anticonvulsant drug level decreased9331.5
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 markerserious n=75no trial arm names this drug
Granulocytopenia37131.3
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 — unassessedserious n=346 · 100% clinicianno trial arm names this drug
Ammonia increased32230.5
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 markerserious n=202no trial arm names this drug
Anticonvulsant drug level increased9929.3
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 markerserious n=77no trial arm names this drug
Diabetic coma17028.9
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 — unassessedserious n=170no trial arm names this drug
Deformity56328.9
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 — unassessedserious PRR 26.7 · 90% consumerno trial arm names this drug
Hypomania21728.3
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 — unassessedserious n=189 · ♀ 78% (drug 52%)no trial arm names this drug
Diabetes mellitus non-insulin-dependent8226.7
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 — unassessedserious n=76no trial arm names this drug
Motor developmental delay3226.6
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=32no trial arm names this drug
Tension32725.6
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% consumerno trial arm names this drug
Autism5525.5
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 disorder11625.3
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=102no trial arm names this drug
Hyperammonaemic encephalopathy8623.9
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% clinicianno trial arm names this drug
Cogwheel rigidity5223.5
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 — unassessedserious n=49 · ♀ 29% (drug 52%) · 100% clinicianno trial arm names this drug
Bipolar disorder52222.7
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 19.2no trial arm names this drug
Seizure cluster3822.4
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=34no trial arm names this drug
Complex partial seizures5021.0
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=46no trial arm names this drug
Compulsive sexual behaviour3520.2
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 — unassessedserious n=33no trial arm names this drug
Congenital anomaly32419.6
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% consumerno trial arm names this drug
Mania66719.1
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 15.4no trial arm names this drug
Drug level fluctuating3518.8
13.4–26.3ROR 18.8 · calibrated p 0.003 ✓
17.8 EB05 13.3 · IC025 +3.3
3/3 methods agree
Reporting / coding artifact100% clinicianno trial arm names this drug

Trial evidence (ClinicalTrials.gov)

ClinicalTrials.gov returned results-bearing trials mentioning Divalproex only as a background or rescue medication (NCT01064297, NCT00261443); no trial listing it as the tested intervention was cached, so no trial cross-check is shown.

Most frequently reported reactions

By raw co-report count, regardless of disproportionality. Common terms here are often the illness itself or generic outcomes.

ReactionReportsPRR 95% CI · ROR · χ²/pEBGM EB05 · IC025Label screenSerious-only & strataTrial cross-check
Drug ineffective (drug did not work)3,0441.0
1.0–1.1ROR 1.1 · calibrated p 0.340
1.0 EB05 1.0 · IC025 +0.0Reporting / coding artifactserious PRR 1.5no trial arm names this drug
Seizure2,62010.6
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 8.5no trial arm names this drug
Nausea2,1091.2
1.2–1.3ROR 1.2 · calibrated p 0.455
1.2 EB05 1.2 · IC025 +0.2Labeled adverse reaction
exact term
serious PRR 1.4no trial arm names this drug
Off label use (used outside approved label)2,0821.1
1.0–1.1ROR 1.1 · calibrated p 0.367
1.1 EB05 1.0 · IC025 +0.0Reporting / coding artifactserious PRR 1.2no trial arm names this drug
Somnolence (drowsiness)1,9004.3
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 4.0no trial arm names this drug
Pain1,8981.4
1.3–1.5ROR 1.4 · calibrated p 0.586
1.4 EB05 1.3 · IC025 +0.4Labeled adverse reaction
exact term
serious PRR 1.6no trial arm names this drug
Tremor (shaking)1,8245.0
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 4.4no trial arm names this drug
Fall1,7762.4
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 — unassessedserious PRR 2.2no trial arm names this drug
Anxiety1,7152.7
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 2.7no trial arm names this drug
Vomiting1,6411.6
1.5–1.7ROR 1.6 · calibrated p 0.713
1.6 EB05 1.5 · IC025 +0.6Labeled — boxed warning
exact term
serious PRR 1.6no trial arm names this drug
Headache1,5991.2
1.1–1.2ROR 1.2 · calibrated p 0.415
1.2 EB05 1.1 · IC025 +0.1Labeled — boxed warning
exact term
serious PRR 1.3no trial arm names this drug
Convulsion (seizure)1,56212.5
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 9.8no trial arm names this drug
Depression1,5593.1
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 2.9no 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.

✓ 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

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.