Valproic Acid side effects: what 31,329 FDA adverse event reports show
Drug class
Anti-epileptic Agent, Mood Stabilizer
Who reports
31,329 reports · 94% serious · 4,621 with death outcome · 46% female
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 .
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.
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 (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). 1,165 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 | 40 | 586.2 382.9–897.3ROR 586.9 · calibrated p 1e-13 ✓ | 270.6 EB05 207.3 · IC025 +5.5 3/3 methods agree vs other Anti-epileptic Agents: PRR 18.3 (11.5–29.0) | Labeled (related wording) related wording | serious n=40 · ♀ 100% (drug 46%) | no trial arm names this drug |
| Paroxysmal perceptual alteration | 21 | 355.1 208.9–603.5ROR 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 — unassessed | serious n=21 · 100% clinician | no trial arm names this drug |
| New onset refractory status epilepticus | 31 | 276.3 181.7–420.1ROR 276.5 · calibrated p 1e-10 ✓ | 174.2 EB05 128.6 · IC025 +5.0 3/3 methods agree vs other Anti-epileptic Agents: PRR 3.9 (2.6–5.7) | Labeled (related wording) related wording | serious n=31 · ♀ 0% (drug 46%) · 100% clinician | no trial arm names this drug |
| Hyperammonaemic encephalopathy | 471 | 254.6 229.0–283.0ROR 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 — unassessed | serious n=470 · 98% clinician | no trial arm names this drug |
| Intra-abdominal pressure increased | 35 | 192.3 132.0–280.2ROR 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 marker | serious n=35 · ♀ 100% (drug 46%) | no trial arm names this drug |
| Carnitine deficiency | 37 | 189.1 131.3–272.6ROR 189.4 · calibrated p 2e-9 ✓ | 136.9 EB05 103.8 · IC025 +5.1 3/3 methods agree vs other Anti-epileptic Agents: only this drug | Labeled (related wording) related wording | serious n=36 · ♀ 71% (drug 46%) · 100% clinician | no trial arm names this drug |
| Foetal anticonvulsant syndrome | 218 | 148.8 128.5–172.3ROR 149.9 · calibrated p 5e-9 ✓ | 120.3 EB05 107.5 · IC025 +6.4 3/3 methods agree vs other Anti-epileptic Agents: PRR 9.7 (8.2–11.5) | Labeled (related wording) related wording | serious n=218 · 93% clinician | no trial arm names this drug |
| Multiple-drug resistance | 537 | 140.7 128.3–154.3ROR 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 artifact | serious n=447 · 95% clinician | no trial arm names this drug |
| Csf oligoclonal band present | 21 | 138.5 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 marker | serious n=21 · ♀ 100% (drug 46%) | no trial arm names this drug |
| Eosinophilic pleural effusion | 43 | 112.5 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 — unassessed | serious n=42 · 100% clinician | no trial arm names this drug |
| Congenital nose malformation | 77 | 112.1 88.1–142.7ROR 112.4 · calibrated p 7e-8 ✓ | 93.8 EB05 77.5 · IC025 +5.5 3/3 methods agree vs other Anti-epileptic Agents: PRR 232.1 (93.9–573.4) | Labeled (related wording) related wording | serious n=77 · 92% clinician | no trial arm names this drug |
| Anticonvulsant drug level above therapeutic | 93 | 111.3 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 marker | serious n=93 · 90% clinician | no trial arm names this drug |
| Postictal psychosis | 22 | 110.7 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 — unassessed | serious n=22 · ♀ 0% (drug 46%) · 100% clinician | no trial arm names this drug |
| Decreased eye contact | 39 | 98.9 70.7–138.5ROR 99.0 · calibrated p 3e-7 ✓ | 82.8 EB05 63.2 · IC025 +4.8 3/3 methods agree vs other Anti-epileptic Agents: only this drug | Labeled (related wording) related wording | serious n=39 · ♀ 0% (drug 46%) · 100% clinician | no trial arm names this drug |
| Hyperammonaemia | 624 | 95.6 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 — unassessed | serious n=613 · 96% clinician | no trial arm names this drug |
| Renal fusion anomaly | 19 | 92.1 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 — unassessed | serious n=19 | no trial arm names this drug |
| Necrosis ischaemic | 54 | 88.4 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 — unassessed | serious n=54 · ♀ 68% (drug 46%) | no trial arm names this drug |
| Myoclonic epilepsy | 157 | 79.8 67.7–94.2ROR 80.2 · calibrated p 7e-7 ✓ | 70.7 EB05 61.9 · IC025 +5.6 3/3 methods agree vs other Anti-epileptic Agents: PRR 3.0 (2.6–3.6) | Labeled (related wording) related wording | serious n=157 · 94% clinician | no trial arm names this drug |
| Schizoaffective disorder | 180 | 74.7 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 — unassessed | serious n=180 · ♀ 87% (drug 46%) | no trial arm names this drug |
| Lennox-gastaut syndrome | 22 | 72.5 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 — unassessed | serious n=22 | no trial arm names this drug |
| Epileptic encephalopathy | 21 | 70.3 44.8–110.2ROR 70.3 · calibrated p 4e-6 ✓ | 60.3 EB05 41.6 · IC025 +4.0 3/3 methods agree vs other Anti-epileptic Agents: PRR 4.2 (2.6–6.7) | Labeled (related wording) related wording | serious n=21 · 100% clinician | no trial arm names this drug |
| Vascular encephalopathy | 27 | 69.6 46.8–103.4ROR 69.6 · calibrated p 4e-6 ✓ | 60.5 EB05 43.6 · IC025 +4.2 3/3 methods agree vs other Anti-epileptic Agents: only this drug | Labeled (related wording) related wording | serious n=27 · ♀ 100% (drug 46%) | no trial arm names this drug |
| Neovascularisation | 24 | 69.1 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 — unassessed | serious n=24 · ♀ 100% (drug 46%) · 100% clinician | no trial arm names this drug |
| Propofol infusion syndrome | 65 | 67.8 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 — unassessed | serious n=65 · ♀ 83% (drug 46%) · 90% clinician | no trial arm names this drug |
| Failure to suspend medication | 19 | 67.7 42.2–108.6ROR 67.8 · calibrated p 6e-6 ✓ | 58.1 EB05 39.3 · IC025 +3.8 3/3 methods agree vs other Anti-epileptic Agents: only this drug | Labeled (related wording) related wording | serious n=19 | no trial arm names this drug |
| Congenital oral malformation | 20 | 66.9 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=20 | no trial arm names this drug |
| Postictal paralysis | 22 | 66.9 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 — unassessed | serious n=22 · 100% clinician | no trial arm names this drug |
| Oppositional defiant disorder | 34 | 62.3 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 — unassessed | serious n=34 · ♀ 0% (drug 46%) · 100% clinician | no trial arm names this drug |
| Sinus rhythm | 37 | 61.6 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 — unassessed | serious n=37 · ♀ 100% (drug 46%) · 100% clinician | no trial arm names this drug |
| Partial seizures with secondary generalisation | 39 | 60.7 43.7–84.2ROR 60.7 · calibrated p 7e-6 ✓ | 54.2 EB05 41.4 · IC025 +4.5 3/3 methods agree vs other Anti-epileptic Agents: PRR 1.6 (1.2–2.3) | Labeled (related wording) related wording | serious n=39 · 100% clinician | no trial arm names this drug |
| Skull malformation | 54 | 60.5 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% clinician | no trial arm names this drug |
| Oscillopsia | 21 | 58.7 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 — unassessed | serious n=21 · 100% clinician | no trial arm names this drug |
| Acidosis hyperchloraemic | 47 | 58.0 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 — unassessed | serious n=47 · 100% clinician | no trial arm names this drug |
| Dysmorphism | 188 | 57.3 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 — unassessed | serious n=188 · 91% clinician | no trial arm names this drug |
| Central sleep apnoea syndrome | 25 | 56.8 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 — unassessed | serious n=25 · 100% clinician | no trial arm names this drug |
| Atonic seizures | 59 | 53.4 41.0–69.7ROR 53.5 · calibrated p 1e-5 ✓ | 48.8 EB05 39.2 · IC025 +4.7 3/3 methods agree vs other Anti-epileptic Agents: PRR 2.0 (1.5–2.6) | Labeled (related wording) related wording | serious n=58 | no trial arm names this drug |
| Psychiatric decompensation | 143 | 52.9 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 — unassessed | serious n=143 · ♀ 0% (drug 46%) · 94% clinician | no trial arm names this drug |
| Postural tremor | 20 | 49.8 31.6–78.4ROR 49.8 · calibrated p 3e-5 ✓ | 44.5 EB05 30.4 · IC025 +3.7 3/3 methods agree vs other Anti-epileptic Agents: PRR 37.7 (16.6–85.5) | Labeled (related wording) related wording | serious n=18 | no trial arm names this drug |
| Anticonvulsant drug level increased | 111 | 49.0 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 marker | serious n=107 · 90% clinician | no trial arm names this drug |
| Pneumatosis | 30 | 48.4 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 — unassessed | serious n=30 · ♀ 100% (drug 46%) | 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) | 3,770 | 1.9 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 artifact | serious PRR 3.2 · 91% clinician | no trial arm names this drug |
| Drug interaction | 3,528 | 15.2 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 artifact | serious PRR 10.1 · 91% clinician | no trial arm names this drug |
| Off label use (used outside approved label) | 2,160 | 1.7 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 artifact | serious PRR 1.8 | no trial arm names this drug |
| Toxicity to various agents | 1,996 | 8.0 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 — unassessed | serious PRR 5.0 · 96% clinician | no trial arm names this drug |
| Seizure | 1,941 | 11.5 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 7.1 | no trial arm names this drug |
| Completed suicide (death by suicide) | 1,306 | 10.5 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% clinician | no trial arm names this drug |
| Somnolence (drowsiness) | 1,277 | 4.3 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 4.2 | no trial arm names this drug |
| Depression | 1,226 | 3.6 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 aggravated | 1,054 | 2.3 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 artifact | serious PRR 2.1 · 91% clinician | no trial arm names this drug |
| Overdose | 950 | 2.9 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 artifact | serious PRR 2.2 · 93% clinician | no trial arm names this drug |
| Foetal exposure during pregnancy | 903 | 7.5 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 artifact | serious PRR 4.6 · 94% clinician | no trial arm names this drug |
| Pyrexia (fever) | 881 | 1.7 1.6–1.8ROR 1.7 · calibrated p 0.785 | 1.7 EB05 1.6 · IC025 +0.7 vs other Anti-epileptic Agents: PRR 1.2 (1.2–1.3) | Labeled (related wording) related wording | serious PRR 1.3 | no trial arm names this drug |
| Product use in unapproved indication | 850 | 2.3 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 artifact | serious PRR 2.7 | no trial arm names this drug |
| Status epilepticus | 757 | 47.9 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 27.4 | no trial arm names this drug |
| Vomiting | 711 | 1.0 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 0.9 | 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.
- Paroxysmal perceptual alteration — n=21, PRR 355.1
- Hyperammonaemic encephalopathy — n=471, PRR 254.6
- Eosinophilic pleural effusion — n=43, PRR 112.5
- Postictal psychosis — n=22, PRR 110.7
- Hyperammonaemia — n=624, PRR 95.6
- Necrosis ischaemic — n=54, PRR 88.4
- Schizoaffective disorder — n=180, PRR 74.7
- Lennox-gastaut syndrome — n=22, PRR 72.5
- Neovascularisation — n=24, PRR 69.1
- Propofol infusion syndrome — n=65, PRR 67.8
✓ 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
- FDA label via openFDA (set ID 2314af65-b928-42a9-91eb-6372909ab4f5, effective 20260331; matched on
openfda.generic_name.exact:"VALPROIC ACID") - 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, 1,205 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
VALPROIC ACID, 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.