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Moxifloxacin side effects: what 14,003 FDA adverse event reports show

Moxifloxacin · 1,133 reaction terms · 87,212 drug–reaction co-reports · data 2026-09-14
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Drug class

Not stated in label

Who reports

14,003 reports · 85% serious · 1,997 with death outcome · 55% female

openFDA FAERS counts, all years, deduplication not applied

Used for

Moxifloxacin tablets are a fluoroquinolone antibacterial indicated for treating infections in adults 18 years of age and older caused by designated susceptible bacteria, in the conditions listed below: Community Acquired Pneumonia ( 1.1 ) Skin and Skin.

FDA label, Indications and Usage

What it is

Moxifloxacin hydrochloride USP is a synthetic antibacterial agent for oral administration. Moxifloxacin, a fluoroquinolone, is available as the monohydrochloride salt of 1-cyclopropyl-7-[(S,S)-2,8-diazabicyclo[4.3.0]non-8-yl]-6-fluoro-8-methoxy-1,4-dihydro-4-oxo-3 quinoline carboxylic acid.

FDA label, Description section

Boxed warning

SERIOUS ADVERSE REACTIONS INCLUDING TENDINITIS, TENDON RUPTURE, PERIPHERAL NEUROPATHY, CENTRAL NERVOUS SYSTEM EFFECTS andEXACERBATION OF MYASTHENIA GRAVIS Fluoroquinolones, including moxifloxacin tablets, have been a.

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) 2Likely indication confounding 2Lab value / disease marker 3Not in label — unassessed 33
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). 1,093 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
Npm1 gene mutation118,120.9
1,800.1–36,635.2ROR 8,127.3 · calibrated p 6e-15 ✓
393.1 EB05 234.2 · IC025 +3.5
3/3 methods agree
Not in label — unassessedserious n=11no trial data cached
Iris transillumination defect961,629.3
1,219.5–2,176.6ROR 1,640.5 · calibrated p 3e-19 ✓
670.7 EB05 565.5 · IC025 +6.9
3/3 methods agree
Not in label — unassessedserious n=94 · 100% clinicianno trial data cached
Spirometry abnormal172622.5
521.3–743.3ROR 630.2 · calibrated p 7e-15 ✓
417.7 EB05 367.9 · IC025 +7.3
3/3 methods agree
Lab value / disease markerserious n=172 · ♀ 0% (drug 55%)no trial data cached
Mite allergy162511.1
427.8–610.6ROR 517.1 · calibrated p 6e-14 ✓
363.6 EB05 319.0 · IC025 +7.2
3/3 methods agree
Not in label — unassessedserious n=162 · ♀ 0% (drug 55%)no trial data cached
Total lung capacity increased67487.3
369.9–642.0ROR 489.7 · calibrated p 2e-13 ✓
331.9 EB05 270.4 · IC025 +6.2
3/3 methods agree
Not in label — unassessedserious n=67 · ♀ 100% (drug 55%) · 93% clinicianno trial data cached
Pulmonary vasculitis116421.9
343.4–518.2ROR 425.4 · calibrated p 5e-13 ✓
311.5 EB05 266.7 · IC025 +6.8
3/3 methods agree
Not in label — unassessedserious n=116 · ♀ 0% (drug 55%)no trial data cached
Sleep disorder due to general medical condition, hypersomnia type20373.8
228.9–610.4ROR 374.3 · calibrated p 2e-11 ✓
232.4 EB05 158.9 · IC025 +4.4
3/3 methods agree
Not in label — unassessedserious n=20no trial data cached
Type 2 lepra reaction37366.7
255.9–525.3ROR 367.6 · calibrated p 6e-12 ✓
255.2 EB05 193.4 · IC025 +5.4
3/3 methods agree
Not in label — unassessedserious n=37 · ♀ 0% (drug 55%) · 100% clinicianno trial data cached
Mycotic allergy164362.5
305.8–429.7ROR 366.8 · calibrated p 2e-12 ✓
281.7 EB05 247.3 · IC025 +7.0
3/3 methods agree
Not in label — unassessedserious n=164 · ♀ 0% (drug 55%)no trial data cached
Total lung capacity abnormal71343.7
265.6–444.8ROR 345.5 · calibrated p 5e-12 ✓
259.5 EB05 212.7 · IC025 +6.2
3/3 methods agree
Not in label — unassessedserious n=71 · ♀ 0% (drug 55%)no trial data cached
Dust allergy168316.4
268.1–373.5ROR 320.2 · calibrated p 7e-12 ✓
253.2 EB05 222.7 · IC025 +6.9
3/3 methods agree
Not in label — unassessedserious n=168 · ♀ 0% (drug 55%)no trial data cached
Keratitis fungal33290.0
199.8–421.1ROR 290.7 · calibrated p 6e-11 ✓
212.8 EB05 158.6 · IC025 +5.1
3/3 methods agree
Not in label — unassessedserious n=32 · 100% clinicianno trial data cached
Iris hypopigmentation17285.2
169.7–479.3ROR 285.6 · calibrated p 2e-10 ✓
188.8 EB05 124.8 · IC025 +4.1
3/3 methods agree
Not in label — unassessedserious n=16no trial data cached
Capillaritis42278.1
200.1–386.5ROR 278.9 · calibrated p 6e-11 ✓
211.7 EB05 163.2 · IC025 +5.5
3/3 methods agree
Not in label — unassessedserious n=42 · ♀ 0% (drug 55%)no trial data cached
Infective keratitis11275.3
144.6–523.9ROR 275.5 · calibrated p 1e-9 ✓
165.9 EB05 98.9 · IC025 +3.4
3/3 methods agree
Not in label — unassessedserious n=11no trial data cached
Choroiditis58273.6
206.8–361.9ROR 274.7 · calibrated p 5e-11 ✓
214.7 EB05 172.2 · IC025 +5.8
3/3 methods agree
Not in label — unassessedserious n=58 · ♀ 18% (drug 55%) · 91% clinicianno trial data cached
Persistent corneal epithelial defect16243.5
143.6–413.2ROR 243.8 · calibrated p 9e-10 ✓
167.7 EB05 109.4 · IC025 +4.0
3/3 methods agree
Not in label — unassessedserious n=12no trial data cached
Mycobacterial peritonitis13234.1
130.4–420.1ROR 234.3 · calibrated p 2e-9 ✓
156.3 EB05 97.2 · IC025 +3.6
3/3 methods agree
Not in label — unassessedserious n=13no trial data cached
Asthma-chronic obstructive pulmonary disease overlap syndrome70232.8
181.0–299.4ROR 233.9 · calibrated p 2e-10 ✓
190.8 EB05 156.1 · IC025 +6.0
3/3 methods agree
Not in label — unassessedserious n=70 · ♀ 100% (drug 55%) · 93% clinicianno trial data cached
Pigment dispersion syndrome12221.5
120.8–406.2ROR 221.7 · calibrated p 4e-9 ✓
147.9 EB05 90.2 · IC025 +3.5
3/3 methods agree
Not in label — unassessedserious n=12no trial data cached
Chimerism11210.9
112.2–396.7ROR 211.1 · calibrated p 7e-9 ✓
140.3 EB05 83.6 · IC025 +3.3
3/3 methods agree
Not in label — unassessedserious n=11no trial data cached
C-reactive protein111208.8
171.3–254.5ROR 210.4 · calibrated p 4e-10 ✓
177.5 EB05 151.5 · IC025 +6.3
3/3 methods agree
Lab value / disease markerserious n=111 · ♀ 100% (drug 55%) · 92% clinicianno trial data cached
Conjunctivitis allergic167193.1
164.5–226.7ROR 195.4 · calibrated p 6e-10 ✓
167.6 EB05 147.4 · IC025 +6.6
3/3 methods agree
Not in label — unassessedserious n=167 · ♀ 0% (drug 55%)no trial data cached
Grip strength24172.9
113.3–263.8ROR 173.2 · calibrated p 6e-9 ✓
138.1 EB05 97.6 · IC025 +4.5
3/3 methods agree
Not in label — unassessedserious n=24no trial data cached
Disseminated mycobacterium avium complex infection22172.8
111.1–268.6ROR 173.1 · calibrated p 7e-9 ✓
136.7 EB05 95.1 · IC025 +4.4
3/3 methods agree
Not in label — unassessedserious n=22 · 100% clinicianno trial data cached
Mycobacterium fortuitum infection19171.1
106.4–275.0ROR 171.3 · calibrated p 1e-8 ✓
133.2 EB05 90.1 · IC025 +4.2
3/3 methods agree
Not in label — unassessedserious n=19no trial data cached
Antineutrophil cytoplasmic antibody positive69156.7
122.4–200.8ROR 157.5 · calibrated p 5e-9 ✓
136.5 EB05 111.5 · IC025 +5.7
3/3 methods agree
Lab value / disease markerserious n=69 · ♀ 0% (drug 55%)no trial data cached
Rhodococcus infection15147.7
86.9–251.0ROR 147.8 · calibrated p 4e-8 ✓
115.0 EB05 74.0 · IC025 +3.8
3/3 methods agree
Not in label — unassessedserious n=15no trial data cached
Keratitis bacterial14143.6
82.9–248.4ROR 143.7 · calibrated p 6e-8 ✓
111.4 EB05 70.5 · IC025 +3.7
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=13no trial data cached
Immune reconstitution inflammatory syndrome associated tuberculosis26126.7
84.9–189.0ROR 126.9 · calibrated p 6e-8 ✓
107.7 EB05 77.3 · IC025 +4.5
3/3 methods agree
Not in label — unassessedserious n=26 · 100% clinicianno trial data cached
Mycobacterium abscessus infection55126.7
96.2–166.8ROR 127.2 · calibrated p 3e-8 ✓
112.3 EB05 89.5 · IC025 +5.4
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=55 · 100% clinicianno trial data cached
Necrotising scleritis11123.0
66.5–227.6ROR 123.1 · calibrated p 3e-7 ✓
95.4 EB05 56.8 · IC025 +3.2
3/3 methods agree
Not in label — unassessedserious n=11no trial data cached
Neuritis116122.1
101.1–147.4ROR 123.1 · calibrated p 3e-8 ✓
110.8 EB05 94.9 · IC025 +5.9
3/3 methods agree
Not in label — unassessedserious n=116 · ♀ 0% (drug 55%)no trial data cached
Swollen joint count18118.1
73.1–190.9ROR 118.3 · calibrated p 2e-7 ✓
98.3 EB05 65.8 · IC025 +4.0
3/3 methods agree
Not in label — unassessedserious n=18no trial data cached
Deep vein thrombosis postoperative139114.2
96.2–135.6ROR 115.3 · calibrated p 5e-8 ✓
104.6 EB05 90.8 · IC025 +6.0
3/3 methods agree
Not in label — unassessedserious n=139 · ♀ 100% (drug 55%)no trial data cached
Nasal oedema126113.2
94.5–135.5ROR 114.2 · calibrated p 5e-8 ✓
103.6 EB05 89.3 · IC025 +5.9
3/3 methods agree
Not in label — unassessedserious n=126 · ♀ 100% (drug 55%) · 96% clinicianno trial data cached
Corneal decompensation11112.0
60.7–206.7ROR 112.1 · calibrated p 5e-7 ✓
88.6 EB05 52.8 · IC025 +3.2
3/3 methods agree
Not in label — unassessedserious n=11no trial data cached
Corneal infiltrates21109.2
70.1–170.0ROR 109.3 · calibrated p 2e-7 ✓
93.3 EB05 64.4 · IC025 +4.2
3/3 methods agree
Not in label — unassessedserious n=20 · 100% clinicianno trial data cached

Trial evidence (ClinicalTrials.gov)

Trial cross-check not yet run for this drug (ClinicalTrials.gov pull covers the 800 most-reported drugs first).

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
Off label use (used outside approved label)1,4522.5
2.4–2.6ROR 2.7 · calibrated p 0.739
2.5 EB05 2.4 · IC025 +1.2
3/3 methods agree
Reporting / coding artifactserious PRR 2.8no trial data cached
Drug ineffective (drug did not work)1,4131.6
1.5–1.7ROR 1.7 · calibrated p 0.754
1.6 EB05 1.5 · IC025 +0.6Reporting / coding artifactserious PRR 2.9no trial data cached
Dyspnoea (shortness of breath)1,2883.4
3.2–3.6ROR 3.7 · calibrated p 0.447
3.4 EB05 3.3 · IC025 +1.7
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 3.2no trial data cached
Pneumonia (lung infection)1,2075.6
5.3–5.9ROR 6.0 · calibrated p 0.147
5.6 EB05 5.3 · IC025 +2.4
3/3 methods agree
Likely indication confounding
term in indications
serious PRR 3.9 · ♀ 81% (drug 55%)no trial data cached
Vomiting1,1763.8
3.6–4.0ROR 4.0 · calibrated p 0.375
3.8 EB05 3.6 · IC025 +1.8
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 3.7 · ♀ 87% (drug 55%)no trial data cached
Asthma96413.0
12.2–13.8ROR 13.9 · calibrated p 0.010 ✓
12.9 EB05 12.2 · IC025 +3.6
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 12.2 · ♀ 78% (drug 55%)no trial data cached
Pain8782.1
2.0–2.3ROR 2.2 · calibrated p 0.944
2.1 EB05 2.0 · IC025 +1.0
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 2.2 · ♀ 86% (drug 55%)no trial data cached
Nausea8671.6
1.5–1.8ROR 1.7 · calibrated p 0.762
1.6 EB05 1.6 · IC025 +0.6Labeled adverse reaction
exact term
serious PRR 2.0 · ♀ 76% (drug 55%)no trial data cached
Wheezing84721.7
20.4–23.2ROR 23.1 · calibrated p 0.001 ✓
21.4 EB05 20.2 · IC025 +4.3
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 20.0 · ♀ 77% (drug 55%)no trial data cached
Rash7802.7
2.5–2.9ROR 2.8 · calibrated p 0.696
2.7 EB05 2.5 · IC025 +1.3
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 3.7 · ♀ 85% (drug 55%)no trial data cached
Condition aggravated7783.9
3.6–4.1ROR 4.0 · calibrated p 0.372
3.8 EB05 3.6 · IC025 +1.8
3/3 methods agree
Reporting / coding artifactserious PRR 3.8no trial data cached
Fatigue (tiredness)7731.5
1.4–1.6ROR 1.5 · calibrated p 0.654
1.5 EB05 1.4 · IC025 +0.5Labeled — boxed warning
synonym match
serious PRR 1.8no trial data cached
Diarrhoea (diarrhea)7431.7
1.6–1.9ROR 1.8 · calibrated p 0.813
1.7 EB05 1.6 · IC025 +0.7Labeled adverse reaction
exact term
serious PRR 1.9 · ♀ 75% (drug 55%)no trial data cached
Malaise (feeling unwell)7142.4
2.3–2.6ROR 2.5 · calibrated p 0.808
2.4 EB05 2.3 · IC025 +1.2
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 2.7 · ♀ 91% (drug 55%)no trial data cached

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 Moxifloxacin?

In FDA FAERS, the most frequently co-reported reaction terms for Moxifloxacin are dyspnoea, pneumonia, vomiting, drug hypersensitivity, asthma, pain. 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 Moxifloxacin have an FDA boxed warning?

Yes. The current FDA label carries a boxed warning: SERIOUS ADVERSE REACTIONS INCLUDING TENDINITIS, TENDON RUPTURE, PERIPHERAL NEUROPATHY, CENTRAL NERVOUS SYSTEM EFFECTS andEXACERBATION OF MYASTHENIA GRAVIS Fluoroquinolones, including moxifloxacin tablets, have been a.

Do FAERS signals prove that Moxifloxacin 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.