Lithium side effects: what 25,059 FDA adverse event reports show
Drug class
Mood-stabilizing agent
Who reports
25,059 reports · 78% serious · 2,094 with death outcome · 58% female
Used for
Lithium oral solution is a mood-stabilizing agent indicated as monotherapy for the treatment of bipolar I disorder: Treatment of acute manic and mixed episodes in patients 7 years and older . Maintenance treatment in patients 7 years and older .
What it is
Each 5 mL of solution for oral administration contains lithium ion (Li + ), 8 mEq (equivalent to amount of lithium in 300 mg of lithium carbonate, USP), and the following other inactive ingred.
Boxed warning
LITHIUM TOXICITY Lithium toxicity is closely related to serum lithium concentrations, and can occur at doses close to therapeutic concentrations. Facilities for prompt and accurate serum lithium determinations should be available before initiating treatment [see Dosage and Administration ( 2.3 ), Warnings and Precautions ( 5.1 ) ] .
Causality screen of the 40 strongest signals
What the badges mean
- Labeled — boxed warning The term (or its clinical synonym) appears in the FDA boxed warning: causality is regulator-recognised and considered serious.
- Labeled adverse reaction The exact term appears in the label's warnings or adverse-reactions sections: a known, expected effect. The FAERS signal confirms the label rather than discovering anything.
- 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.
- 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). 1,181 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 |
|---|---|---|---|---|---|---|
| Hypokinetic dysarthria | 16 | 1,884.7 775.4–4,580.9ROR 1,885.9 · calibrated p 2e-15 ✓ | 340.3 EB05 222.1 · IC025 +4.1 3/3 methods agree | Not in label — unassessed | serious n=16 | not reported in cached trials |
| Paroxysmal perceptual alteration | 25 | 589.0 352.6–983.9ROR 589.6 · calibrated p 3e-13 ✓ | 272.4 EB05 194.0 · IC025 +4.8 3/3 methods agree | Not in label — unassessed | serious n=25 · ♀ 36% (drug 58%) · 100% clinician | not reported in cached trials |
| Total lung capacity increased | 97 | 462.3 360.7–592.6ROR 464.1 · calibrated p 3e-13 ✓ | 280.2 EB05 236.5 · IC025 +6.5 3/3 methods agree | Not in label — unassessed | serious n=97 · ♀ 100% (drug 58%) · 94% clinician | not reported in cached trials |
| Nephrogenic diabetes insipidus | 304 | 301.3 264.4–343.4ROR 305.0 · calibrated p 1e-11 ✓ | 217.9 EB05 198.1 · IC025 +7.2 3/3 methods agree | Labeled adverse reaction exact term | serious n=302 · 97% clinician | not reported in cached trials |
| Dystonic tremor | 17 | 203.2 119.5–345.3ROR 203.3 · calibrated p 4e-9 ✓ | 138.2 EB05 91.4 · IC025 +4.0 3/3 methods agree | Not in label — unassessed | serious n=17 | not reported in cached trials |
| Asthma-chronic obstructive pulmonary disease overlap syndrome | 97 | 191.8 153.8–239.1ROR 192.5 · calibrated p 9e-10 ✓ | 151.2 EB05 127.6 · IC025 +6.1 3/3 methods agree | Not in label — unassessed | serious n=97 · ♀ 100% (drug 58%) · 94% clinician | not reported in cached trials |
| Delusion of grandeur | 82 | 187.8 147.8–238.6ROR 188.4 · calibrated p 1e-9 ✓ | 147.9 EB05 123.0 · IC025 +6.0 3/3 methods agree | Not in label — unassessed | serious n=82 · ♀ 17% (drug 58%) | not reported in cached trials |
| Antipsychotic drug level below therapeutic | 123 | 180.1 148.3–218.9ROR 181.0 · calibrated p 1e-9 ✓ | 144.7 EB05 124.5 · IC025 +6.2 3/3 methods agree | Lab value / disease marker | serious n=114 · ♀ 22% (drug 58%) | not reported in cached trials |
| Action tremor | 25 | 157.4 102.6–241.3ROR 157.5 · calibrated p 1e-8 ✓ | 120.4 EB05 85.7 · IC025 +4.5 3/3 methods agree | Labeled (related wording) related wording | serious n=25 · 100% clinician | not reported in cached trials |
| Schizoaffective disorder bipolar type | 27 | 110.8 74.1–165.5ROR 110.9 · calibrated p 2e-7 ✓ | 91.6 EB05 66.1 · IC025 +4.5 3/3 methods agree | Likely indication confounding shares a disease stem with the indications wording | serious n=27 | not reported in cached trials |
| Antipsychotic drug level above therapeutic | 104 | 109.7 89.4–134.5ROR 110.1 · calibrated p 7e-8 ✓ | 95.3 EB05 80.9 · IC025 +5.7 3/3 methods agree | Lab value / disease marker | serious n=90 · 91% clinician | not reported in cached trials |
| Camptocormia | 27 | 106.5 71.4–159.0ROR 106.6 · calibrated p 2e-7 ✓ | 88.7 EB05 64.0 · IC025 +4.5 3/3 methods agree | Not in label — unassessed | serious n=25 · ♀ 100% (drug 58%) · 100% clinician | not reported in cached trials |
| Decreased eye contact | 32 | 98.8 68.5–142.6ROR 98.9 · calibrated p 3e-7 ✓ | 84.1 EB05 62.3 · IC025 +4.6 3/3 methods agree | Labeled (related wording) related wording | serious n=32 · ♀ 0% (drug 58%) · 100% clinician | not reported in cached trials |
| Rebound psychosis | 21 | 91.6 58.4–143.8ROR 91.7 · calibrated p 8e-7 ✓ | 77.0 EB05 53.1 · IC025 +4.1 3/3 methods agree | Not in label — unassessed | serious n=21 | not reported in cached trials |
| Grandiosity | 35 | 89.1 62.9–126.2ROR 89.2 · calibrated p 6e-7 ✓ | 77.2 EB05 58.0 · IC025 +4.7 3/3 methods agree | Not in label — unassessed | serious n=34 | not reported in cached trials |
| Postural tremor | 27 | 86.3 58.1–128.3ROR 86.4 · calibrated p 9e-7 ✓ | 74.3 EB05 53.6 · IC025 +4.4 3/3 methods agree | Not in label — unassessed | serious n=27 · 100% clinician | not reported in cached trials |
| Failure to suspend medication | 19 | 84.7 52.8–135.8ROR 84.7 · calibrated p 1e-6 ✓ | 71.6 EB05 48.4 · IC025 +3.9 3/3 methods agree | Labeled (related wording) related wording | serious n=19 | not reported in cached trials |
| Hypomania | 334 | 83.3 74.5–93.2ROR 84.4 · calibrated p 4e-7 ✓ | 75.4 EB05 68.9 · IC025 +5.9 3/3 methods agree | Not in label — unassessed | serious n=315 · ♀ 80% (drug 58%) | not reported in cached trials |
| Adulterated product | 17 | 81.0 49.2–133.3ROR 81.1 · calibrated p 2e-6 ✓ | 68.4 EB05 45.2 · IC025 +3.8 3/3 methods agree | Not in label — unassessed | serious n=17 | not reported in cached trials |
| Oppositional defiant disorder | 35 | 80.4 56.8–113.7ROR 80.5 · calibrated p 1e-6 ✓ | 70.6 EB05 53.1 · IC025 +4.6 3/3 methods agree | Not in label — unassessed | serious n=35 · ♀ 0% (drug 58%) · 100% clinician | not reported in cached trials |
| Schizoaffective disorder | 157 | 80.3 68.2–94.5ROR 80.8 · calibrated p 6e-7 ✓ | 72.6 EB05 63.6 · IC025 +5.6 3/3 methods agree | Not in label — unassessed | serious n=156 | not reported in cached trials |
| Antipsychotic drug level increased | 241 | 78.3 68.6–89.3ROR 79.0 · calibrated p 7e-7 ✓ | 71.2 EB05 64.0 · IC025 +5.8 3/3 methods agree | Lab value / disease marker | serious n=220 | not reported in cached trials |
| Oscillopsia | 21 | 73.4 47.0–114.6ROR 73.4 · calibrated p 3e-6 ✓ | 63.7 EB05 44.0 · IC025 +4.0 3/3 methods agree | Not in label — unassessed | serious n=19 · 100% clinician | not reported in cached trials |
| Antipsychotic drug level decreased | 41 | 69.8 50.8–96.1ROR 70.0 · calibrated p 3e-6 ✓ | 62.7 EB05 48.2 · IC025 +4.7 3/3 methods agree | Lab value / disease marker | serious n=32 · ♀ 0% (drug 58%) · 100% clinician | not reported in cached trials |
| Pleurothotonus | 62 | 61.0 47.1–78.9ROR 61.2 · calibrated p 5e-6 ✓ | 55.9 EB05 45.2 · IC025 +4.9 3/3 methods agree | Not in label — unassessed | serious n=61 · ♀ 100% (drug 58%) · 100% clinician | not reported in cached trials |
| Hyperparathyroidism | 134 | 58.2 48.8–69.3ROR 58.5 · calibrated p 6e-6 ✓ | 54.0 EB05 46.7 · IC025 +5.2 3/3 methods agree | Labeled — boxed warning exact term | serious n=131 · ♀ 83% (drug 58%) · 90% clinician | not reported in cached trials |
| Pressure of speech | 41 | 56.3 41.0–77.2ROR 56.3 · calibrated p 1e-5 ✓ | 51.5 EB05 39.6 · IC025 +4.5 3/3 methods agree | Labeled (related wording) related wording | serious n=40 | not reported in cached trials |
| Bipolar ii disorder | 22 | 54.5 35.4–83.9ROR 54.5 · calibrated p 2e-5 ✓ | 49.1 EB05 34.2 · IC025 +3.9 3/3 methods agree | Likely indication confounding term in indications; also in warnings | serious n=20 | not reported in cached trials |
| Soft tissue injury | 45 | 52.8 39.1–71.3ROR 52.9 · calibrated p 1e-5 ✓ | 48.7 EB05 37.9 · IC025 +4.5 3/3 methods agree | Not in label — unassessed | serious n=45 · ♀ 100% (drug 58%) | not reported in cached trials |
| Bipolar i disorder | 119 | 48.1 40.0–57.8ROR 48.3 · calibrated p 2e-5 ✓ | 45.2 EB05 38.7 · IC025 +5.0 3/3 methods agree | Likely indication confounding term in indications; also in warnings | serious n=109 | not reported in cached trials |
| Post-traumatic neck syndrome | 44 | 47.8 35.3–64.8ROR 47.9 · calibrated p 3e-5 ✓ | 44.4 EB05 34.5 · IC025 +4.4 3/3 methods agree | Not in label — unassessed | serious n=44 · ♀ 100% (drug 58%) | not reported in cached trials |
| Neuroleptic malignant syndrome | 620 | 46.0 42.5–49.8ROR 47.1 · calibrated p 2e-5 ✓ | 43.6 EB05 40.8 · IC025 +5.3 3/3 methods agree | Labeled adverse reaction exact term | serious PRR 32.4 | not reported in cached trials |
| Oromandibular dystonia | 37 | 45.2 32.5–62.9ROR 45.3 · calibrated p 4e-5 ✓ | 42.0 EB05 31.9 · IC025 +4.2 3/3 methods agree | Not in label — unassessed | serious n=35 | not reported in cached trials |
| Echolalia | 16 | 44.0 26.6–72.7ROR 44.0 · calibrated p 8e-5 ✓ | 40.0 EB05 26.1 · IC025 +3.4 3/3 methods agree | Not in label — unassessed | serious n=16 | not reported in cached trials |
| Diabetes insipidus | 121 | 44.0 36.6–52.8ROR 44.2 · calibrated p 3e-5 ✓ | 41.5 EB05 35.7 · IC025 +4.9 3/3 methods agree | Labeled adverse reaction exact term | serious n=119 | not reported in cached trials |
| Somatic symptom disorder | 54 | 44.0 33.4–57.8ROR 44.0 · calibrated p 4e-5 ✓ | 41.2 EB05 32.8 · IC025 +4.5 3/3 methods agree | Not in label — unassessed | serious n=47 · ♀ 100% (drug 58%) | not reported in cached trials |
| Mania | 781 | 41.7 38.9–44.8ROR 43.0 · calibrated p 3e-5 ✓ | 39.7 EB05 37.4 · IC025 +5.2 3/3 methods agree | Not in label — unassessed | serious PRR 31.2 | not reported in cached trials |
| Flight of ideas | 25 | 41.6 27.9–62.2ROR 41.7 · calibrated p 8e-5 ✓ | 38.6 EB05 27.5 · IC025 +3.8 3/3 methods agree | Not in label — unassessed | serious n=25 | not reported in cached trials |
| Disinhibition | 76 | 41.4 32.9–52.1ROR 41.5 · calibrated p 5e-5 ✓ | 39.1 EB05 32.2 · IC025 +4.6 3/3 methods agree | Not in label — unassessed | serious n=76 · ♀ 0% (drug 58%) | not reported in cached trials |
| Lymphocyte count abnormal | 53 | 41.2 31.2–54.2ROR 41.2 · calibrated p 6e-5 ✓ | 38.7 EB05 30.8 · IC025 +4.4 3/3 methods agree | Lab value / disease marker | serious n=53 · ♀ 0% (drug 58%) · 100% clinician | not reported in cached trials |
Trial evidence (ClinicalTrials.gov)
✓ Trial adverse-event data found on ClinicalTrials.gov
Largest completed trials with posted results that list Lithium as a study intervention. The right-hand column of the signal table shows whether each FAERS term was also recorded in these trials, with a real denominator (0 of 40 signal terms matched).
- NCT02960763 — Optimizing Outcomes of Treatment-Resistant Depression in Older Adults (N=742, PHASE4; 23 AE terms posted; arms: Aripiprazole Augmentation; Bupropion Augmentation; Switch to Bupropion; Lithium Augmentation)
Caveats: trial populations, doses and follow-up differ from the reporting population; AE terms are sponsor-coded and matched here by wording; absence from a trial list means the term was not reported above the sponsor's frequency threshold, not that it cannot occur.
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) | 2,297 | 1.5 1.4–1.5ROR 1.5 · calibrated p 0.646 | 1.5 EB05 1.4 · IC025 +0.5 | Reporting / coding artifact | serious PRR 2.3 | not reported in cached trials |
| Toxicity to various agents | 2,267 | 11.4 11.0–11.9ROR 12.5 · calibrated p 0.014 ✓ | 11.3 EB05 10.9 · IC025 +3.4 3/3 methods agree | Not in label — unassessed | serious PRR 8.5 · 92% clinician | not reported in cached trials |
| Off label use (used outside approved label) | 1,604 | 1.5 1.5–1.6ROR 1.6 · calibrated p 0.697 | 1.5 EB05 1.5 · IC025 +0.5 | Reporting / coding artifact | serious PRR 1.7 | not reported in cached trials |
| Drug interaction | 1,582 | 8.4 8.0–8.8ROR 8.9 · calibrated p 0.047 ✓ | 8.3 EB05 8.0 · IC025 +3.0 3/3 methods agree | Reporting / coding artifact | serious PRR 6.4 | not reported in cached trials |
| Tremor (shaking) | 1,509 | 7.7 7.3–8.0ROR 8.1 · calibrated p 0.065 | 7.6 EB05 7.3 · IC025 +2.8 3/3 methods agree | Labeled — boxed warning exact term | serious PRR 7.0 | NCT02960763: 34/127 (26.8%) on Lithium |
| Nausea | 1,406 | 1.5 1.4–1.6ROR 1.5 · calibrated p 0.655 | 1.5 EB05 1.4 · IC025 +0.5 | Labeled adverse reaction exact term | serious PRR 1.6 | NCT02960763: 12/127 (9.4%) on Lithium |
| Weight increased (weight gain) | 1,189 | 4.5 4.2–4.7ROR 4.7 · calibrated p 0.275 | 4.5 EB05 4.2 · IC025 +2.1 3/3 methods agree | Labeled (related wording) related wording | serious PRR 4.7 | NCT02960763: 8/127 (6.3%) on Lithium |
| Fatigue (tiredness) | 1,082 | 1.2 1.1–1.2ROR 1.2 · calibrated p 0.422 | 1.2 EB05 1.1 · IC025 +0.1 | Labeled adverse reaction exact term | serious PRR 1.2 | not reported in cached trials |
| Vomiting | 1,069 | 1.9 1.8–2.0ROR 2.0 · calibrated p 0.917 | 1.9 EB05 1.8 · IC025 +0.8 | Labeled adverse reaction exact term | serious PRR 1.8 | NCT02960763: 12/127 (9.4%) on Lithium |
| Depression | 1,006 | 3.7 3.5–3.9ROR 3.8 · calibrated p 0.416 | 3.7 EB05 3.5 · IC025 +1.8 3/3 methods agree | Labeled (related wording) related wording | serious PRR 3.1 | not reported in cached trials |
| Anxiety | 990 | 2.9 2.7–3.1ROR 3.0 · calibrated p 0.630 | 2.9 EB05 2.8 · IC025 +1.4 3/3 methods agree | Not in label — unassessed | serious PRR 2.5 | not reported in cached trials |
| Somnolence (drowsiness) | 936 | 3.9 3.7–4.2ROR 4.0 · calibrated p 0.374 | 3.9 EB05 3.7 · IC025 +1.9 3/3 methods agree | Labeled — boxed warning synonym match | serious PRR 3.8 | not reported in cached trials |
| Insomnia (trouble sleeping) | 930 | 2.9 2.7–3.1ROR 3.0 · calibrated p 0.627 | 2.9 EB05 2.8 · IC025 +1.4 3/3 methods agree | Not in label — unassessed | serious PRR 2.8 | not reported in cached trials |
| Suicidal ideation (thoughts of suicide) | 914 | 8.4 7.9–9.0ROR 8.7 · calibrated p 0.051 | 8.3 EB05 7.9 · IC025 +2.9 3/3 methods agree | Not in label — unassessed | serious PRR 6.3 | not reported in cached trials |
| Dizziness | 842 | 1.4 1.3–1.5ROR 1.4 · calibrated p 0.596 | 1.4 EB05 1.3 · IC025 +0.4 | Labeled adverse reaction exact term | serious PRR 1.3 | NCT02960763: 28/127 (22.0%) on Lithium |
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=25, PRR 589.0
- Total lung capacity increased — n=97, PRR 462.3
- Asthma-chronic obstructive pulmonary disease overlap syndrome — n=97, PRR 191.8
- Delusion of grandeur — n=82, PRR 187.8
- Camptocormia — n=27, PRR 106.5
- Rebound psychosis — n=21, PRR 91.6
- Grandiosity — n=35, PRR 89.1
- Postural tremor — n=27, PRR 86.3
- Hypomania — n=334, PRR 83.3
- Oppositional defiant disorder — n=35, PRR 80.4
✓ A hand-written Bradford Hill causality assessment exists for this drug: Lithium ↔ Nephrogenic diabetes insipidus.
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 Lithium?
In FDA FAERS, the most frequently co-reported reaction terms for Lithium are toxicity to various agents, tremor, nausea, weight increased, fatigue, vomiting. 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 Lithium have an FDA boxed warning?
Yes. The current FDA label carries a boxed warning: LITHIUM TOXICITY Lithium toxicity is closely related to serum lithium concentrations, and can occur at doses close to therapeutic concentrations. Facilities for prompt and accurate serum lithium determinations should be available before initiating treatment [see Dosage and Administration ( 2.3 ), Warnings and Precautions ( 5.1 ) ] .
Do FAERS signals prove that Lithium 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 e95036c7-542a-437a-969b-f95f6f949f84, effective 20250820; matched on
openfda.generic_name.exact:"LITHIUM") - 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, 1,221 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
LITHIUM, 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.