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Valproic Acid side effects: what 31,329 FDA adverse event reports show

Valproic Acid · 1,205 reaction terms · 116,012 drug–reaction co-reports · data 2026-09-14
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Drug class

Anti-epileptic Agent, Mood Stabilizer

FDA label (Established Pharmacologic Class) · compare the class

Who reports

31,329 reports · 94% serious · 4,621 with death outcome · 46% female

openFDA FAERS counts, all years, deduplication not applied

Used for

Valproic acid oral solution is indicated for: • Monotherapy and adjunctive therapy of complex partial seizures; sole and adjunctive therapy of simple and complex absence seizures; adjunctive therapy in patients with multiple seizure types that include .

FDA label, Indications and Usage

What it is

Valproic acid is a carboxylic acid designated as 2-propylpentanoic acid. It is also known as dipropylacetic acid. Valproic acid has the following structure: Valproic acid (pKa 4.8) has a molecular weight of 144 and occurs as a colorless liquid with a characteristic odor.

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 (related wording) 13Likely indication confounding 2Reporting / coding artifact 1Lab value / disease marker 4Not in label — unassessed 20
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). 1,165 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
Paroxysmal perceptual alteration21355.1
208.9–603.5ROR 355.3 · calibrated p 4e-11 ✓
191.2 EB05 131.9 · IC025 +4.5
3/3 methods agree
vs other Anti-epileptic Agents: only this drug
Not in label — unassessedserious n=21 · 100% clinicianno trial arm names this drug
Hyperammonaemic encephalopathy471254.6
229.0–283.0ROR 258.5 · calibrated p 4e-11 ✓
182.6 EB05 169.2 · IC025 +7.1
3/3 methods agree
vs other Anti-epileptic Agents: PRR 39.2 (33.1–46.5)
Not in label — unassessedserious n=470 · 98% clinicianno trial arm names this drug
Intra-abdominal pressure increased35192.3
132.0–280.2ROR 192.6 · calibrated p 2e-9 ✓
138.1 EB05 103.8 · IC025 +5.0
3/3 methods agree
vs other Anti-epileptic Agents: PRR 15.1 (9.4–24.1)
Lab value / disease markerserious n=35 · ♀ 100% (drug 46%)no trial arm names this drug
Multiple-drug resistance537140.7
128.3–154.3ROR 143.1 · calibrated p 7e-9 ✓
115.7 EB05 107.7 · IC025 +6.6
3/3 methods agree
vs other Anti-epileptic Agents: PRR 2.9 (2.7–3.2)
Reporting / coding artifactserious n=447 · 95% clinicianno trial arm names this drug
Csf oligoclonal band present21138.5
86.5–221.7ROR 138.6 · calibrated p 5e-8 ✓
104.0 EB05 71.8 · IC025 +4.2
3/3 methods agree
vs other Anti-epileptic Agents: PRR 9.0 (5.3–15.5)
Lab value / disease markerserious n=21 · ♀ 100% (drug 46%)no trial arm names this drug
Eosinophilic pleural effusion43112.5
81.4–155.5ROR 112.7 · calibrated p 1e-7 ✓
92.4 EB05 71.5 · IC025 +5.0
3/3 methods agree
vs other Anti-epileptic Agents: only this drug
Not in label — unassessedserious n=42 · 100% clinicianno trial arm names this drug
Anticonvulsant drug level above therapeutic93111.3
89.4–138.6ROR 111.6 · calibrated p 7e-8 ✓
93.6 EB05 78.7 · IC025 +5.6
3/3 methods agree
vs other Anti-epileptic Agents: PRR 3.0 (2.4–3.7)
Lab value / disease markerserious n=93 · 90% clinicianno trial arm names this drug
Postictal psychosis22110.7
70.5–173.9ROR 110.8 · calibrated p 2e-7 ✓
87.9 EB05 61.2 · IC025 +4.2
3/3 methods agree
vs other Anti-epileptic Agents: PRR 3.0 (1.9–4.7)
Not in label — unassessedserious n=22 · ♀ 0% (drug 46%) · 100% clinicianno trial arm names this drug
Hyperammonaemia62495.6
87.9–103.9ROR 97.5 · calibrated p 1e-7 ✓
83.4 EB05 78.0 · IC025 +6.2
3/3 methods agree
vs other Anti-epileptic Agents: PRR 13.8 (12.4–15.4)
Not in label — unassessedserious n=613 · 96% clinicianno trial arm names this drug
Renal fusion anomaly1992.1
57.0–148.9ROR 92.2 · calibrated p 8e-7 ✓
75.1 EB05 50.8 · IC025 +4.0
3/3 methods agree
vs other Anti-epileptic Agents: only this drug
Not in label — unassessedserious n=19no trial arm names this drug
Necrosis ischaemic5488.4
66.5–117.4ROR 88.5 · calibrated p 5e-7 ✓
76.0 EB05 60.5 · IC025 +5.1
3/3 methods agree
vs other Anti-epileptic Agents: PRR 15.1 (10.3–22.0)
Not in label — unassessedserious n=54 · ♀ 68% (drug 46%)no trial arm names this drug
Schizoaffective disorder18074.7
64.0–87.1ROR 75.1 · calibrated p 1e-6 ✓
66.7 EB05 58.9 · IC025 +5.6
3/3 methods agree
vs other Anti-epileptic Agents: PRR 117.9 (76.4–182.0)
Not in label — unassessedserious n=180 · ♀ 87% (drug 46%)no trial arm names this drug
Lennox-gastaut syndrome2272.5
46.7–112.6ROR 72.6 · calibrated p 3e-6 ✓
62.1 EB05 43.2 · IC025 +4.0
3/3 methods agree
vs other Anti-epileptic Agents: PRR 5.8 (3.6–9.5)
Not in label — unassessedserious n=22no trial arm names this drug
Neovascularisation2469.1
45.4–105.2ROR 69.2 · calibrated p 4e-6 ✓
59.8 EB05 42.3 · IC025 +4.1
3/3 methods agree
vs other Anti-epileptic Agents: only this drug
Not in label — unassessedserious n=24 · ♀ 100% (drug 46%) · 100% clinicianno trial arm names this drug
Propofol infusion syndrome6567.8
52.6–87.5ROR 68.0 · calibrated p 3e-6 ✓
60.5 EB05 49.2 · IC025 +5.0
3/3 methods agree
vs other Anti-epileptic Agents: PRR 12.1 (8.7–16.8)
Not in label — unassessedserious n=65 · ♀ 83% (drug 46%) · 90% clinicianno trial arm names this drug
Congenital oral malformation2066.9
42.3–106.0ROR 67.0 · calibrated p 6e-6 ✓
57.7 EB05 39.4 · IC025 +3.9
3/3 methods agree
vs other Anti-epileptic Agents: only this drug
Likely indication confounding
term in indications; also in warnings
serious n=20no trial arm names this drug
Postictal paralysis2266.9
43.1–103.6ROR 66.9 · calibrated p 6e-6 ✓
57.9 EB05 40.3 · IC025 +4.0
3/3 methods agree
vs other Anti-epileptic Agents: PRR 4.9 (3.0–7.9)
Not in label — unassessedserious n=22 · 100% clinicianno trial arm names this drug
Oppositional defiant disorder3462.3
43.8–88.5ROR 62.3 · calibrated p 6e-6 ✓
55.3 EB05 41.4 · IC025 +4.4
3/3 methods agree
vs other Anti-epileptic Agents: only this drug
Not in label — unassessedserious n=34 · ♀ 0% (drug 46%) · 100% clinicianno trial arm names this drug
Sinus rhythm3761.6
44.0–86.3ROR 61.7 · calibrated p 6e-6 ✓
54.9 EB05 41.6 · IC025 +4.5
3/3 methods agree
vs other Anti-epileptic Agents: only this drug
Not in label — unassessedserious n=37 · ♀ 100% (drug 46%) · 100% clinicianno trial arm names this drug
Skull malformation5460.5
45.8–79.9ROR 60.6 · calibrated p 6e-6 ✓
54.5 EB05 43.3 · IC025 +4.8
3/3 methods agree
vs other Anti-epileptic Agents: only this drug
Likely indication confounding
shares a disease stem with the indications wording
serious n=54 · 91% clinicianno trial arm names this drug
Oscillopsia2158.7
37.6–91.7ROR 58.7 · calibrated p 1e-5 ✓
51.6 EB05 35.6 · IC025 +3.9
3/3 methods agree
vs other Anti-epileptic Agents: only this drug
Not in label — unassessedserious n=21 · 100% clinicianno trial arm names this drug
Acidosis hyperchloraemic4758.0
43.1–78.2ROR 58.1 · calibrated p 8e-6 ✓
52.4 EB05 41.0 · IC025 +4.6
3/3 methods agree
vs other Anti-epileptic Agents: PRR 39.3 (22.9–67.7)
Not in label — unassessedserious n=47 · 100% clinicianno trial arm names this drug
Dysmorphism18857.3
49.4–66.5ROR 57.7 · calibrated p 6e-6 ✓
52.6 EB05 46.6 · IC025 +5.3
3/3 methods agree
vs other Anti-epileptic Agents: PRR 4.0 (3.4–4.7)
Not in label — unassessedserious n=188 · 91% clinicianno trial arm names this drug
Central sleep apnoea syndrome2556.8
37.8–85.5ROR 56.9 · calibrated p 1e-5 ✓
50.5 EB05 36.0 · IC025 +4.0
3/3 methods agree
vs other Anti-epileptic Agents: only this drug
Not in label — unassessedserious n=25 · 100% clinicianno trial arm names this drug
Psychiatric decompensation14352.9
44.6–62.7ROR 53.1 · calibrated p 1e-5 ✓
48.7 EB05 42.4 · IC025 +5.1
3/3 methods agree
vs other Anti-epileptic Agents: only this drug
Not in label — unassessedserious n=143 · ♀ 0% (drug 46%) · 94% clinicianno trial arm names this drug
Anticonvulsant drug level increased11149.0
40.4–59.4ROR 49.1 · calibrated p 2e-5 ✓
45.3 EB05 38.7 · IC025 +4.9
3/3 methods agree
vs other Anti-epileptic Agents: PRR 1.9 (1.6–2.4)
Lab value / disease markerserious n=107 · 90% clinicianno trial arm names this drug
Pneumatosis3048.4
33.4–70.1ROR 48.4 · calibrated p 3e-5 ✓
44.0 EB05 32.3 · IC025 +4.1
3/3 methods agree
vs other Anti-epileptic Agents: PRR 13.7 (8.4–22.5)
Not in label — unassessedserious n=30 · ♀ 100% (drug 46%)no trial arm names this drug

Trial evidence (ClinicalTrials.gov)

ClinicalTrials.gov returned results-bearing trials mentioning Valproic Acid 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)3,7701.9
1.9–2.0ROR 2.0 · calibrated p 0.968
1.9 EB05 1.9 · IC025 +0.9
vs other Anti-epileptic Agents: PRR 1.7 (1.7–1.8)
Reporting / coding artifactserious PRR 3.2 · 91% clinicianno trial arm names this drug
Drug interaction3,52815.2
14.7–15.7ROR 17.0 · calibrated p 0.004 ✓
14.9 EB05 14.5 · IC025 +3.8
3/3 methods agree
vs other Anti-epileptic Agents: PRR 3.5 (3.4–3.7)
Reporting / coding artifactserious PRR 10.1 · 91% clinicianno trial arm names this drug
Off label use (used outside approved label)2,1601.7
1.6–1.7ROR 1.7 · calibrated p 0.780
1.7 EB05 1.6 · IC025 +0.7
vs other Anti-epileptic Agents: PRR 1.8 (1.7–1.9)
Reporting / coding artifactserious PRR 1.8no trial arm names this drug
Toxicity to various agents1,9968.0
7.7–8.4ROR 8.5 · calibrated p 0.055
7.9 EB05 7.7 · IC025 +2.9
3/3 methods agree
vs other Anti-epileptic Agents: PRR 2.0 (1.9–2.1)
Not in label — unassessedserious PRR 5.0 · 96% clinicianno trial arm names this drug
Seizure1,94111.5
11.0–12.0ROR 12.2 · calibrated p 0.016 ✓
11.3 EB05 10.9 · IC025 +3.4
3/3 methods agree
vs other Anti-epileptic Agents: PRR 1.2 (1.1–1.2)
Labeled — boxed warning
exact term
serious PRR 7.1no trial arm names this drug
Completed suicide (death by suicide)1,30610.5
10.0–11.1ROR 11.0 · calibrated p 0.023 ✓
10.4 EB05 9.9 · IC025 +3.3
3/3 methods agree
vs other Anti-epileptic Agents: PRR 1.9 (1.8–2.0)
Outcome field, not a reaction
boxed warning mentions mortality
serious PRR 6.3 · 99% clinicianno trial arm names this drug
Somnolence (drowsiness)1,2774.3
4.0–4.5ROR 4.4 · calibrated p 0.309
4.2 EB05 4.1 · IC025 +2.0
3/3 methods agree
vs other Anti-epileptic Agents: PRR 1.4 (1.3–1.5)
Labeled adverse reaction
exact term
serious PRR 4.2no trial arm names this drug
Depression1,2263.6
3.4–3.8ROR 3.7 · calibrated p 0.436
3.6 EB05 3.4 · IC025 +1.7
3/3 methods agree
vs other Anti-epileptic Agents: PRR 1.6 (1.5–1.7)
Labeled adverse reaction
exact term
serious PRR 3.0 · ♀ 15% (drug 46%)no trial arm names this drug
Condition aggravated1,0542.3
2.2–2.5ROR 2.4 · calibrated p 0.863
2.3 EB05 2.2 · IC025 +1.1
3/3 methods agree
vs other Anti-epileptic Agents: PRR 1.5 (1.4–1.6)
Reporting / coding artifactserious PRR 2.1 · 91% clinicianno trial arm names this drug
Overdose9502.9
2.8–3.1ROR 3.0 · calibrated p 0.625
2.9 EB05 2.8 · IC025 +1.4
3/3 methods agree
vs other Anti-epileptic Agents: PRR 1.9 (1.8–2.0)
Reporting / coding artifactserious PRR 2.2 · 93% clinicianno trial arm names this drug
Foetal exposure during pregnancy9037.5
7.0–8.0ROR 7.7 · calibrated p 0.075
7.4 EB05 7.0 · IC025 +2.8
3/3 methods agree
vs other Anti-epileptic Agents: PRR 1.4 (1.3–1.5)
Reporting / coding artifactserious PRR 4.6 · 94% clinicianno trial arm names this drug
Product use in unapproved indication8502.3
2.2–2.5ROR 2.4 · calibrated p 0.870
2.3 EB05 2.2 · IC025 +1.1
3/3 methods agree
vs other Anti-epileptic Agents: PRR 2.0 (1.8–2.1)
Reporting / coding artifactserious PRR 2.7no trial arm names this drug
Status epilepticus75747.9
44.6–51.6ROR 49.1 · calibrated p 2e-5 ✓
44.7 EB05 42.1 · IC025 +5.3
3/3 methods agree
vs other Anti-epileptic Agents: PRR 2.6 (2.4–2.8)
Labeled adverse reaction
exact term
serious PRR 27.4no trial arm names this drug
Vomiting7111.0
0.9–1.1ROR 1.0 · calibrated p 0.317
1.0 EB05 1.0 · IC025 -0.1
PRR-only: not supported by EBGM or IC
vs other Anti-epileptic Agents: PRR 0.9 (0.8–0.9)
Labeled — boxed warning
exact term
serious PRR 0.9no 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: Zoledronic acid (bisphosphonates) ↔ Osteonecrosis of the jaw.

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 Valproic Acid?

In FDA FAERS, the most frequently co-reported reaction terms for Valproic Acid are toxicity to various agents, seizure, somnolence, depression, pyrexia, status epilepticus. 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 Valproic Acid 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 Valproic Acid 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.