← All drugs
Drug · FAERS side-effect profile with label screen

Gabapentin side effects: what 362,501 FDA adverse event reports show

Gabapentin · 1,137 reaction terms · 1,437,988 drug–reaction co-reports · data 2026-09-14
Share: X Facebook Reddit Email

Drug class

Not stated in label

Who reports

362,501 reports · 63% serious · 34,219 with death outcome · 65% female

openFDA FAERS counts, all years, deduplication not applied

Used for

Gabapentin is indicated for: • Management of postherpetic neuralgia in adults • Adjunctive therapy in the treatment of partial onset seizures, with and without secondary generalization, in adults and pediatric patients 3 years and older with epilepsy G.

FDA label, Indications and Usage

What it is

Gabapentin is a gamma-amino acid that is cyclohexane substituted at position 1 by aminomethyl and carboxymethyl groups. Used for treatment of neuropathic pain and restless legs syndrome.

PubChem CID 3446 (ChEBI)

Boxed warning

None in the current 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) 6Likely indication confounding 2Reporting / coding artifact 3Lab value / disease marker 2Not in label — unassessed 27
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). 1,097 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
Appendicolith281167.6
132.7–211.7ROR 167.7 · calibrated p 3e-9 ✓
42.6 EB05 38.6 · IC025 +5.1
3/3 methods agree
Not in label — unassessedserious n=281 · ♀ 0% (drug 65%) · 100% clinicianno trial arm names this drug
Chronic kidney disease-mineral and bone disorder26818.9
16.5–21.7ROR 18.9 · calibrated p 0.003 ✓
14.4 EB05 13.0 · IC025 +3.6
3/3 methods agree
Not in label — unassessedserious n=268no trial arm names this drug
Nephrogenic anaemia1,02015.9
14.8–17.1ROR 16.0 · calibrated p 0.005 ✓
12.6 EB05 12.0 · IC025 +3.5
3/3 methods agree
Not in label — unassessedserious n=1,020no trial arm names this drug
Drug titration error56015.7
14.3–17.3ROR 15.8 · calibrated p 0.006 ✓
12.5 EB05 11.6 · IC025 +3.5
3/3 methods agree
Reporting / coding artifact–no trial arm names this drug
Hyperparathyroidism secondary52414.9
13.5–16.4ROR 14.9 · calibrated p 0.007 ✓
11.9 EB05 11.1 · IC025 +3.4
3/3 methods agree
Not in label — unassessedserious n=523no trial arm names this drug
Rebound acid hypersecretion49010.8
9.8–11.9ROR 10.8 · calibrated p 0.025 ✓
9.2 EB05 8.5 · IC025 +3.0
3/3 methods agree
Not in label — unassessedserious n=490no trial arm names this drug
Infusion site discharge26010.2
8.9–11.6ROR 10.2 · calibrated p 0.031 ✓
8.7 EB05 7.8 · IC025 +2.9
3/3 methods agree
Not in label — unassessed♀ 100% (drug 65%) · 100% consumerno trial arm names this drug
Temperature regulation disorder3119.4
8.4–10.6ROR 9.5 · calibrated p 0.040 ✓
8.2 EB05 7.4 · IC025 +2.8
3/3 methods agree
Not in label — unassessedserious n=301 · ♀ 100% (drug 65%) · 100% clinicianno trial arm names this drug
Diabetic neuropathy7059.4
8.7–10.2ROR 9.4 · calibrated p 0.040 ✓
8.2 EB05 7.7 · IC025 +2.9
3/3 methods agree
Not in label — unassessedserious n=627no trial arm names this drug
Gun shot wound2468.5
7.4–9.7ROR 8.5 · calibrated p 0.057
7.4 EB05 6.7 · IC025 +2.7
3/3 methods agree
Not in label — unassessedserious n=245 · ♀ 0% (drug 65%) · 100% consumerno trial arm names this drug
Drug ineffective for unapproved indication6,3577.3
7.1–7.5ROR 7.4 · calibrated p 0.083
6.6 EB05 6.5 · IC025 +2.7
3/3 methods agree
Reporting / coding artifactage-adj. PRR 7.7 · serious PRR 3.7no trial arm names this drug
Infusion site haemorrhage3637.2
6.4–8.0ROR 7.2 · calibrated p 0.093
6.4 EB05 5.9 · IC025 +2.5
3/3 methods agree
Not in label — unassessed100% consumerno trial arm names this drug
Neuralgia2,6116.9
6.6–7.1ROR 6.9 · calibrated p 0.103
6.2 EB05 6.0 · IC025 +2.6
3/3 methods agree
Likely indication confounding
term in indications; also in warnings
serious PRR 6.2no trial arm names this drug
Myoclonus1,2666.8
6.4–7.2ROR 6.8 · calibrated p 0.108
6.1 EB05 5.8 · IC025 +2.5
3/3 methods agree
Not in label — unassessedage-adj. PRR 6.6 · serious PRR 5.5no trial arm names this drug
Intervertebral disc degeneration9806.7
6.3–7.2ROR 6.7 · calibrated p 0.111
6.1 EB05 5.8 · IC025 +2.5
3/3 methods agree
Not in label — unassessedserious PRR 5.7no trial arm names this drug
End stage renal disease1,9306.7
6.4–7.0ROR 6.7 · calibrated p 0.112
6.1 EB05 5.8 · IC025 +2.5
3/3 methods agree
Not in label — unassessedserious PRR 5.5no trial arm names this drug
Trigeminal neuralgia4126.5
5.9–7.2ROR 6.5 · calibrated p 0.122
5.9 EB05 5.4 · IC025 +2.4
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=327no trial arm names this drug
Pre-existing condition improved6306.3
5.8–6.9ROR 6.3 · calibrated p 0.131
5.7 EB05 5.4 · IC025 +2.4
3/3 methods agree
Not in label — unassessedserious n=340no trial arm names this drug
Device infusion issue2406.2
5.4–7.1ROR 6.2 · calibrated p 0.140
5.6 EB05 5.0 · IC025 +2.3
3/3 methods agree
Reporting / coding artifact♀ 100% (drug 65%) · 100% consumerno trial arm names this drug
Hypertonic bladder2635.7
5.0–6.5ROR 5.7 · calibrated p 0.171
5.2 EB05 4.7 · IC025 +2.2
3/3 methods agree
Not in label — unassessedserious n=224no trial arm names this drug
Blood phosphorus increased2465.6
4.9–6.4ROR 5.6 · calibrated p 0.177
5.2 EB05 4.6 · IC025 +2.2
3/3 methods agree
Lab value / disease markerserious n=233 · ♀ 0% (drug 65%) · 100% clinicianno trial arm names this drug
Lumbar spinal stenosis2595.5
4.9–6.3ROR 5.5 · calibrated p 0.187
5.1 EB05 4.6 · IC025 +2.1
3/3 methods agree
Not in label — unassessedserious n=246no trial arm names this drug
Blood pressure diastolic abnormal2265.5
4.8–6.3ROR 5.5 · calibrated p 0.190
5.0 EB05 4.5 · IC025 +2.1
3/3 methods agree
Lab value / disease markerserious n=224 · 100% clinicianno trial arm names this drug
Radiculopathy2305.4
4.7–6.2ROR 5.4 · calibrated p 0.194
5.0 EB05 4.5 · IC025 +2.1
3/3 methods agree
Not in label — unassessedserious n=211 · ♀ 0% (drug 65%)no trial arm names this drug
Spinal osteoarthritis7385.2
4.8–5.6ROR 5.2 · calibrated p 0.215
4.8 EB05 4.5 · IC025 +2.1
3/3 methods agree
Not in label — unassessedserious PRR 4.4no trial arm names this drug
Sleep apnoea syndrome1,5935.2
4.9–5.4ROR 5.2 · calibrated p 0.215
4.8 EB05 4.6 · IC025 +2.2
3/3 methods agree
Not in label — unassessedage-adj. PRR 4.7 · serious PRR 4.8no trial arm names this drug
Chronic kidney disease6,2685.1
4.9–5.2ROR 5.1 · calibrated p 0.220
4.7 EB05 4.6 · IC025 +2.2
3/3 methods agree
Not in label — unassessedage-adj. PRR 4.1 · serious PRR 4.4no trial arm names this drug
Infusion site pruritus2464.9
4.3–5.5ROR 4.9 · calibrated p 0.250
4.5 EB05 4.1 · IC025 +2.0
3/3 methods agree
Not in label — unassessed♀ 100% (drug 65%) · 100% consumerno trial arm names this drug
Fibromyalgia1,8804.8
4.6–5.0ROR 4.8 · calibrated p 0.258
4.5 EB05 4.3 · IC025 +2.1
3/3 methods agree
Not in label — unassessedserious PRR 4.1 · ♀ 92% (drug 65%)no trial arm names this drug
Spinal stenosis3144.7
4.2–5.3ROR 4.7 · calibrated p 0.266
4.4 EB05 4.0 · IC025 +2.0
3/3 methods agree
Not in label — unassessedserious n=283no trial arm names this drug
Hypopnoea2664.7
4.2–5.4ROR 4.7 · calibrated p 0.266
4.4 EB05 4.0 · IC025 +1.9
3/3 methods agree
Not in label — unassessedserious n=236 · ♀ 0% (drug 65%) · 100% clinicianno trial arm names this drug
Nerve injury8574.7
4.4–5.1ROR 4.7 · calibrated p 0.265
4.4 EB05 4.2 · IC025 +2.0
3/3 methods agree
Not in label — unassessedserious PRR 4.4no trial arm names this drug
Spinal column stenosis3604.6
4.2–5.1ROR 4.6 · calibrated p 0.280
4.3 EB05 4.0 · IC025 +1.9
3/3 methods agree
Not in label — unassessedserious n=328no trial arm names this drug
Lymphoedema5174.6
4.2–5.0ROR 4.6 · calibrated p 0.282
4.3 EB05 4.0 · IC025 +2.0
3/3 methods agree
Not in label — unassessedserious n=468 · ♀ 100% (drug 65%)no trial arm names this drug

Clinical concept groups

MedDRA splits one clinical problem across several terms (e.g. "neutropenia", "neutrophil count decreased", "agranulocytosis"), which dilutes term-level signals. These rows count reports with any term in a concept group (an exact union, not a sum), compared with all other drugs. Groups are hand-built and listed in the methods.

ConceptReportsPRR 95% CIReading
Suicidality12,4283.03.0–3.1signal
Fall / fracture16,4292.62.5–2.6signal
Depression11,8052.52.4–2.5signal
Extrapyramidal3,3901.91.8–2.0raised
Kidney injury14,5431.91.8–1.9raised
Hyponatraemia2,5171.81.8–1.9raised
Serious infection23,7771.81.8–1.8raised
Seizure5,8721.81.7–1.8raised
Opportunistic infection3,5841.51.5–1.6raised
Venous thromboembolism5,4721.51.4–1.5raised
Anaemia7,2451.41.4–1.4raised
Hypoglycaemia2,2571.41.3–1.4raised
Pancreatitis1,8811.41.3–1.4raised
Gi bleeding4,2521.41.3–1.4raised
Hyperglycaemia / diabetes7,9721.31.3–1.4raised
Tendon disorder8641.31.2–1.4raised

Trial evidence (ClinicalTrials.gov)

ClinicalTrials.gov returned results-bearing trials mentioning Gabapentin only as a background or rescue medication (NCT04294901); 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)29,6341.3
1.3–1.3ROR 1.3 · calibrated p 0.532
1.3 EB05 1.3 · IC025 +0.4Reporting / coding artifactage-adj. PRR 1.5 · serious PRR 1.6no trial arm names this drug
Fatigue (tiredness)25,1401.9
1.9–1.9ROR 2.0 · calibrated p 0.926
1.9 EB05 1.9 · IC025 +0.9Labeled adverse reaction
exact term
age-adj. PRR 1.7 · serious PRR 2.0no trial arm names this drug
Nausea22,7871.7
1.7–1.7ROR 1.7 · calibrated p 0.792
1.7 EB05 1.7 · IC025 +0.7Labeled adverse reaction
exact term
age-adj. PRR 1.5 · serious PRR 1.9no trial arm names this drug
Pain21,2562.0
2.0–2.1ROR 2.1 · calibrated p 0.997
2.0 EB05 2.0 · IC025 +1.0Labeled adverse reaction
exact term
age-adj. PRR 2.1 · serious PRR 2.0no trial arm names this drug
Off label use (used outside approved label)19,8301.3
1.3–1.3ROR 1.3 · calibrated p 0.540
1.3 EB05 1.3 · IC025 +0.4Reporting / coding artifactage-adj. PRR 1.3 · serious PRR 1.4no trial arm names this drug
Diarrhoea (diarrhea)18,1531.7
1.6–1.7ROR 1.7 · calibrated p 0.760
1.6 EB05 1.6 · IC025 +0.7Labeled adverse reaction
exact term
age-adj. PRR 1.5 · serious PRR 1.6no trial arm names this drug
Headache17,9251.7
1.7–1.7ROR 1.7 · calibrated p 0.775
1.7 EB05 1.6 · IC025 +0.7Labeled adverse reaction
exact term
age-adj. PRR 1.5 · serious PRR 1.9no trial arm names this drug
Dizziness16,4461.9
1.9–2.0ROR 2.0 · calibrated p 0.937
1.9 EB05 1.9 · IC025 +0.9Labeled adverse reaction
exact term
age-adj. PRR 1.7 · serious PRR 1.9no trial arm names this drug
Fall15,5582.8
2.7–2.8ROR 2.9 · calibrated p 0.670
2.7 EB05 2.7 · IC025 +1.4
3/3 methods agree
Not in label — unassessedage-adj. PRR 2.5 · serious PRR 2.5no trial arm names this drug
Dyspnoea (shortness of breath)14,2561.5
1.4–1.5ROR 1.5 · calibrated p 0.634
1.5 EB05 1.4 · IC025 +0.5Labeled adverse reaction
exact term
age-adj. PRR 1.3 · serious PRR 1.4no trial arm names this drug
Vomiting12,1801.5
1.5–1.5ROR 1.5 · calibrated p 0.664
1.5 EB05 1.5 · IC025 +0.6Labeled adverse reaction
exact term
age-adj. PRR 1.4 · serious PRR 1.5no trial arm names this drug
Asthenia (weakness)11,9471.9
1.8–1.9ROR 1.9 · calibrated p 0.885
1.8 EB05 1.8 · IC025 +0.8Labeled adverse reaction
exact term
age-adj. PRR 1.6 · serious PRR 1.8no trial arm names this drug
Pain in extremity11,6372.3
2.3–2.4ROR 2.4 · calibrated p 0.867
2.3 EB05 2.2 · IC025 +1.2
3/3 methods agree
Not in label — unassessedage-adj. PRR 2.1 · serious PRR 2.5no trial arm names this drug
Arthralgia (joint pain)11,4981.6
1.6–1.7ROR 1.6 · calibrated p 0.733
1.6 EB05 1.6 · IC025 +0.7Not in label — unassessedage-adj. PRR 1.4 · serious PRR 1.9no trial arm names this drug
Death11,1300.7
0.7–0.8ROR 0.7 · calibrated p 0.149
0.7 EB05 0.7 · IC025 -0.5
PRR-only: not supported by EBGM or IC
Outcome field, not a reactionage-adj. PRR 0.9 · serious PRR 0.7no 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.

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 Gabapentin?

In FDA FAERS, the most frequently co-reported reaction terms for Gabapentin are fatigue, nausea, pain, diarrhoea, headache, dizziness. 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 Gabapentin have an FDA boxed warning?

No. The FDA label retrieved for Gabapentin has no boxed warning; see the label's Warnings and Precautions for the recognised risks.

Do FAERS signals prove that Gabapentin 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.