Gabapentin side effects: what 362,501 FDA adverse event reports show
Drug class
Not stated in label
Who reports
362,501 reports · 63% serious · 34,219 with death outcome · 65% female
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.
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.
Boxed warning
None in the current label
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). 1,097 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 |
|---|---|---|---|---|---|---|
| Appendicolith | 281 | 167.6 132.7–211.7ROR 167.7 · calibrated p 3e-9 ✓ | 42.6 EB05 38.6 · IC025 +5.1 3/3 methods agree | Not in label — unassessed | serious n=281 · ♀ 0% (drug 65%) · 100% clinician | no trial arm names this drug |
| Chronic kidney disease-mineral and bone disorder | 268 | 18.9 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 — unassessed | serious n=268 | no trial arm names this drug |
| Nephrogenic anaemia | 1,020 | 15.9 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 — unassessed | serious n=1,020 | no trial arm names this drug |
| Drug titration error | 560 | 15.7 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 secondary | 524 | 14.9 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 — unassessed | serious n=523 | no trial arm names this drug |
| Rebound acid hypersecretion | 490 | 10.8 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 — unassessed | serious n=490 | no trial arm names this drug |
| Infusion site discharge | 260 | 10.2 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% consumer | no trial arm names this drug |
| Temperature regulation disorder | 311 | 9.4 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 — unassessed | serious n=301 · ♀ 100% (drug 65%) · 100% clinician | no trial arm names this drug |
| Diabetic neuropathy | 705 | 9.4 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 — unassessed | serious n=627 | no trial arm names this drug |
| Gun shot wound | 246 | 8.5 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 — unassessed | serious n=245 · ♀ 0% (drug 65%) · 100% consumer | no trial arm names this drug |
| Accidental death | 229 | 8.0 7.0–9.2ROR 8.0 · calibrated p 0.067 | 7.1 EB05 6.3 · IC025 +2.6 3/3 methods agree | Labeled (related wording) related wording | serious n=229 · 100% clinician | no trial arm names this drug |
| Drug ineffective for unapproved indication | 6,357 | 7.3 7.1–7.5ROR 7.4 · calibrated p 0.083 | 6.6 EB05 6.5 · IC025 +2.7 3/3 methods agree | Reporting / coding artifact | age-adj. PRR 7.7 · serious PRR 3.7 | no trial arm names this drug |
| Infusion site haemorrhage | 363 | 7.2 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 — unassessed | 100% consumer | no trial arm names this drug |
| Neuralgia | 2,611 | 6.9 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 6.2 | no trial arm names this drug |
| Myoclonus | 1,266 | 6.8 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 — unassessed | age-adj. PRR 6.6 · serious PRR 5.5 | no trial arm names this drug |
| Intervertebral disc degeneration | 980 | 6.7 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 — unassessed | serious PRR 5.7 | no trial arm names this drug |
| End stage renal disease | 1,930 | 6.7 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 — unassessed | serious PRR 5.5 | no trial arm names this drug |
| Infusion site infection | 232 | 6.5 5.7–7.4ROR 6.5 · calibrated p 0.123 | 5.9 EB05 5.2 · IC025 +2.3 3/3 methods agree | Labeled (related wording) related wording | ♀ 100% (drug 65%) · 100% consumer | no trial arm names this drug |
| Trigeminal neuralgia | 412 | 6.5 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=327 | no trial arm names this drug |
| Pre-existing condition improved | 630 | 6.3 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 — unassessed | serious n=340 | no trial arm names this drug |
| Device infusion issue | 240 | 6.2 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% consumer | no trial arm names this drug |
| Infusion site pain | 1,220 | 6.0 5.7–6.4ROR 6.0 · calibrated p 0.149 | 5.5 EB05 5.3 · IC025 +2.4 3/3 methods agree | Labeled (related wording) related wording | age-adj. PRR 4.1 · serious n=486 · 83% consumer | no trial arm names this drug |
| Suspected suicide | 441 | 5.8 5.3–6.4ROR 5.8 · calibrated p 0.164 | 5.3 EB05 4.9 · IC025 +2.3 3/3 methods agree | Labeled (related wording) related wording | serious n=441 · 100% clinician | no trial arm names this drug |
| Infusion site swelling | 569 | 5.8 5.3–6.3ROR 5.8 · calibrated p 0.164 | 5.3 EB05 5.0 · IC025 +2.3 3/3 methods agree | Labeled (related wording) related wording | serious n=233 · 100% consumer | no trial arm names this drug |
| Hypertonic bladder | 263 | 5.7 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 — unassessed | serious n=224 | no trial arm names this drug |
| Infusion site erythema | 754 | 5.7 5.3–6.1ROR 5.7 · calibrated p 0.171 | 5.2 EB05 4.9 · IC025 +2.3 3/3 methods agree | Labeled (related wording) related wording | serious n=301 · 84% consumer | no trial arm names this drug |
| Blood phosphorus increased | 246 | 5.6 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 marker | serious n=233 · ♀ 0% (drug 65%) · 100% clinician | no trial arm names this drug |
| Lumbar spinal stenosis | 259 | 5.5 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 — unassessed | serious n=246 | no trial arm names this drug |
| Blood pressure diastolic abnormal | 226 | 5.5 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 marker | serious n=224 · 100% clinician | no trial arm names this drug |
| Radiculopathy | 230 | 5.4 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 — unassessed | serious n=211 · ♀ 0% (drug 65%) | no trial arm names this drug |
| Spinal osteoarthritis | 738 | 5.2 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 — unassessed | serious PRR 4.4 | no trial arm names this drug |
| Sleep apnoea syndrome | 1,593 | 5.2 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 — unassessed | age-adj. PRR 4.7 · serious PRR 4.8 | no trial arm names this drug |
| Chronic kidney disease | 6,268 | 5.1 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 — unassessed | age-adj. PRR 4.1 · serious PRR 4.4 | no trial arm names this drug |
| Infusion site pruritus | 246 | 4.9 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% consumer | no trial arm names this drug |
| Fibromyalgia | 1,880 | 4.8 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 — unassessed | serious PRR 4.1 · ♀ 92% (drug 65%) | no trial arm names this drug |
| Spinal stenosis | 314 | 4.7 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 — unassessed | serious n=283 | no trial arm names this drug |
| Hypopnoea | 266 | 4.7 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 — unassessed | serious n=236 · ♀ 0% (drug 65%) · 100% clinician | no trial arm names this drug |
| Nerve injury | 857 | 4.7 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 — unassessed | serious PRR 4.4 | no trial arm names this drug |
| Spinal column stenosis | 360 | 4.6 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 — unassessed | serious n=328 | no trial arm names this drug |
| Lymphoedema | 517 | 4.6 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 — unassessed | serious 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.
| Concept | Reports | PRR 95% CI | Reading |
|---|---|---|---|
| Suicidality | 12,428 | 3.03.0–3.1 | signal |
| Fall / fracture | 16,429 | 2.62.5–2.6 | signal |
| Depression | 11,805 | 2.52.4–2.5 | signal |
| Extrapyramidal | 3,390 | 1.91.8–2.0 | raised |
| Kidney injury | 14,543 | 1.91.8–1.9 | raised |
| Hyponatraemia | 2,517 | 1.81.8–1.9 | raised |
| Serious infection | 23,777 | 1.81.8–1.8 | raised |
| Seizure | 5,872 | 1.81.7–1.8 | raised |
| Opportunistic infection | 3,584 | 1.51.5–1.6 | raised |
| Venous thromboembolism | 5,472 | 1.51.4–1.5 | raised |
| Anaemia | 7,245 | 1.41.4–1.4 | raised |
| Hypoglycaemia | 2,257 | 1.41.3–1.4 | raised |
| Pancreatitis | 1,881 | 1.41.3–1.4 | raised |
| Gi bleeding | 4,252 | 1.41.3–1.4 | raised |
| Hyperglycaemia / diabetes | 7,972 | 1.31.3–1.4 | raised |
| Tendon disorder | 864 | 1.31.2–1.4 | raised |
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) | 29,634 | 1.3 1.3–1.3ROR 1.3 · calibrated p 0.532 | 1.3 EB05 1.3 · IC025 +0.4 | Reporting / coding artifact | age-adj. PRR 1.5 · serious PRR 1.6 | no trial arm names this drug |
| Fatigue (tiredness) | 25,140 | 1.9 1.9–1.9ROR 2.0 · calibrated p 0.926 | 1.9 EB05 1.9 · IC025 +0.9 | Labeled adverse reaction exact term | age-adj. PRR 1.7 · serious PRR 2.0 | no trial arm names this drug |
| Nausea | 22,787 | 1.7 1.7–1.7ROR 1.7 · calibrated p 0.792 | 1.7 EB05 1.7 · IC025 +0.7 | Labeled adverse reaction exact term | age-adj. PRR 1.5 · serious PRR 1.9 | no trial arm names this drug |
| Pain | 21,256 | 2.0 2.0–2.1ROR 2.1 · calibrated p 0.997 | 2.0 EB05 2.0 · IC025 +1.0 | Labeled adverse reaction exact term | age-adj. PRR 2.1 · serious PRR 2.0 | no trial arm names this drug |
| Off label use (used outside approved label) | 19,830 | 1.3 1.3–1.3ROR 1.3 · calibrated p 0.540 | 1.3 EB05 1.3 · IC025 +0.4 | Reporting / coding artifact | age-adj. PRR 1.3 · serious PRR 1.4 | no trial arm names this drug |
| Diarrhoea (diarrhea) | 18,153 | 1.7 1.6–1.7ROR 1.7 · calibrated p 0.760 | 1.6 EB05 1.6 · IC025 +0.7 | Labeled adverse reaction exact term | age-adj. PRR 1.5 · serious PRR 1.6 | no trial arm names this drug |
| Headache | 17,925 | 1.7 1.7–1.7ROR 1.7 · calibrated p 0.775 | 1.7 EB05 1.6 · IC025 +0.7 | Labeled adverse reaction exact term | age-adj. PRR 1.5 · serious PRR 1.9 | no trial arm names this drug |
| Dizziness | 16,446 | 1.9 1.9–2.0ROR 2.0 · calibrated p 0.937 | 1.9 EB05 1.9 · IC025 +0.9 | Labeled adverse reaction exact term | age-adj. PRR 1.7 · serious PRR 1.9 | no trial arm names this drug |
| Fall | 15,558 | 2.8 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 — unassessed | age-adj. PRR 2.5 · serious PRR 2.5 | no trial arm names this drug |
| Dyspnoea (shortness of breath) | 14,256 | 1.5 1.4–1.5ROR 1.5 · calibrated p 0.634 | 1.5 EB05 1.4 · IC025 +0.5 | Labeled adverse reaction exact term | age-adj. PRR 1.3 · serious PRR 1.4 | no trial arm names this drug |
| Vomiting | 12,180 | 1.5 1.5–1.5ROR 1.5 · calibrated p 0.664 | 1.5 EB05 1.5 · IC025 +0.6 | Labeled adverse reaction exact term | age-adj. PRR 1.4 · serious PRR 1.5 | no trial arm names this drug |
| Asthenia (weakness) | 11,947 | 1.9 1.8–1.9ROR 1.9 · calibrated p 0.885 | 1.8 EB05 1.8 · IC025 +0.8 | Labeled adverse reaction exact term | age-adj. PRR 1.6 · serious PRR 1.8 | no trial arm names this drug |
| Pain in extremity | 11,637 | 2.3 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 — unassessed | age-adj. PRR 2.1 · serious PRR 2.5 | no trial arm names this drug |
| Arthralgia (joint pain) | 11,498 | 1.6 1.6–1.7ROR 1.6 · calibrated p 0.733 | 1.6 EB05 1.6 · IC025 +0.7 | Not in label — unassessed | age-adj. PRR 1.4 · serious PRR 1.9 | no trial arm names this drug |
| Death | 11,130 | 0.7 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 reaction | age-adj. PRR 0.9 · serious PRR 0.7 | 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.
- Appendicolith — n=281, PRR 167.6
- Chronic kidney disease-mineral and bone disorder — n=268, PRR 18.9
- Nephrogenic anaemia — n=1,020, PRR 15.9
- Hyperparathyroidism secondary — n=524, PRR 14.9
- Rebound acid hypersecretion — n=490, PRR 10.8
- Infusion site discharge — n=260, PRR 10.2
- Temperature regulation disorder — n=311, PRR 9.4
- Diabetic neuropathy — n=705, PRR 9.4
- Gun shot wound — n=246, PRR 8.5
- Infusion site haemorrhage — n=363, PRR 7.2
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
- FDA label via openFDA (set ID 03031adf-d36b-45ec-944e-dfce5a5de91a, effective 20260528; matched on
openfda.generic_name.exact:"GABAPENTIN" AND openfda.product_type:"HUMAN PRESCRIPTION DRUG") - PubChem CID 3446 description (ChEBI)
- 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, 1,137 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
GABAPENTIN, 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.