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

Moxifloxacin Hydrochloride side effects: what 20,154 FDA adverse event reports show

Moxifloxacin Hydrochloride · 1,214 reaction terms · 146,081 drug–reaction co-reports · data 2026-09-14
Share: X Facebook Reddit Email

Drug class

Not stated in label

Who reports

20,154 reports · 85% serious · 2,667 with death outcome · 58% 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 1Lab value / disease marker 3Not in label — unassessed 34
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). 1,174 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
Iris transillumination defect1141,694.5
1,257.0–2,284.2ROR 1,704.1 · calibrated p 2e-19 ✓
577.2 EB05 493.6 · IC025 +7.1
3/3 methods agree
Not in label — unassessedserious n=106 · 100% cliniciannot reported in cached trials
Total lung capacity increased1531,341.2
1,054.7–1,705.5ROR 1,351.5 · calibrated p 2e-18 ✓
542.1 EB05 473.7 · IC025 +7.4
3/3 methods agree
Not in label — unassessedserious n=153 · ♀ 100% (drug 58%)not reported in cached trials
Spirometry abnormal286997.7
848.3–1,173.4ROR 1,012.1 · calibrated p 3e-17 ✓
489.6 EB05 443.8 · IC025 +7.9
3/3 methods agree
Lab value / disease markerserious n=286 · ♀ 0% (drug 58%)not reported in cached trials
Mite allergy270769.2
657.3–900.2ROR 779.7 · calibrated p 6e-16 ✓
426.6 EB05 385.6 · IC025 +7.7
3/3 methods agree
Not in label — unassessedserious n=270 · ♀ 0% (drug 58%)not reported in cached trials
Mycotic allergy272498.2
431.3–575.4ROR 505.0 · calibrated p 7e-14 ✓
327.9 EB05 296.5 · IC025 +7.5
3/3 methods agree
Not in label — unassessedserious n=272 · ♀ 0% (drug 58%)not reported in cached trials
Asthma-chronic obstructive pulmonary disease overlap syndrome157451.0
374.0–543.9ROR 454.6 · calibrated p 2e-13 ✓
302.0 EB05 264.4 · IC025 +7.0
3/3 methods agree
Not in label — unassessedserious n=157 · ♀ 100% (drug 58%)not reported in cached trials
Sleep disorder due to general medical condition, hypersomnia type29424.9
275.7–654.9ROR 425.5 · calibrated p 3e-12 ✓
251.1 EB05 183.3 · IC025 +5.0
3/3 methods agree
Not in label — unassessedserious n=29 · ♀ 100% (drug 58%) · 100% cliniciannot reported in cached trials
Dust allergy276418.7
364.3–481.3ROR 424.5 · calibrated p 4e-13 ✓
291.6 EB05 263.9 · IC025 +7.4
3/3 methods agree
Not in label — unassessedserious n=276 · ♀ 0% (drug 58%)not reported in cached trials
Pulmonary vasculitis148405.9
335.7–490.7ROR 408.9 · calibrated p 7e-13 ✓
280.5 EB05 244.6 · IC025 +6.9
3/3 methods agree
Not in label — unassessedserious n=148 · ♀ 0% (drug 58%)not reported in cached trials
Total lung capacity abnormal101376.7
300.0–473.0ROR 378.6 · calibrated p 2e-12 ✓
262.1 EB05 221.9 · IC025 +6.5
3/3 methods agree
Not in label — unassessedserious n=101 · ♀ 0% (drug 58%)not reported in cached trials
Choroiditis93343.1
271.4–433.7ROR 344.7 · calibrated p 5e-12 ✓
244.4 EB05 205.5 · IC025 +6.4
3/3 methods agree
Not in label — unassessedserious n=93 · ♀ 11% (drug 58%)not reported in cached trials
Iris hypopigmentation26337.5
216.8–525.7ROR 338.0 · calibrated p 3e-11 ✓
214.3 EB05 153.7 · IC025 +4.8
3/3 methods agree
Not in label — unassessedserious n=21 · 100% cliniciannot reported in cached trials
Keratitis fungal49330.6
239.7–456.1ROR 331.4 · calibrated p 1e-11 ✓
228.1 EB05 179.3 · IC025 +5.7
3/3 methods agree
Not in label — unassessedserious n=42 · ♀ 36% (drug 58%) · 100% cliniciannot reported in cached trials
Mycobacterial peritonitis21291.1
179.3–472.4ROR 291.4 · calibrated p 1e-10 ✓
188.3 EB05 129.9 · IC025 +4.4
3/3 methods agree
Not in label — unassessedserious n=21not reported in cached trials
Capillaritis57281.1
209.7–376.6ROR 281.9 · calibrated p 4e-11 ✓
205.7 EB05 164.6 · IC025 +5.8
3/3 methods agree
Not in label — unassessedserious n=57 · ♀ 0% (drug 58%)not reported in cached trials
Tender joint count17260.2
152.9–443.0ROR 260.5 · calibrated p 5e-10 ✓
168.7 EB05 111.6 · IC025 +4.1
3/3 methods agree
Not in label — unassessedserious n=17not reported in cached trials
Type 2 lepra reaction37254.7
177.7–365.0ROR 255.2 · calibrated p 2e-10 ✓
184.9 EB05 140.1 · IC025 +5.2
3/3 methods agree
Not in label — unassessedserious n=37 · ♀ 0% (drug 58%) · 100% cliniciannot reported in cached trials
Conjunctivitis allergic279245.6
215.7–279.7ROR 249.1 · calibrated p 6e-11 ✓
195.7 EB05 177.2 · IC025 +7.0
3/3 methods agree
Not in label — unassessedserious n=279 · ♀ 0% (drug 58%)not reported in cached trials
Persistent corneal epithelial defect19207.3
126.6–339.3ROR 207.5 · calibrated p 2e-9 ✓
147.4 EB05 99.7 · IC025 +4.2
3/3 methods agree
Not in label — unassessedserious n=15not reported in cached trials
Toxic anterior segment syndrome173196.7
167.3–231.3ROR 198.4 · calibrated p 5e-10 ✓
162.3 EB05 143.0 · IC025 +6.6
3/3 methods agree
Not in label — unassessedserious n=168 · 91% cliniciannot reported in cached trials
C-reactive protein143194.8
163.0–232.8ROR 196.2 · calibrated p 6e-10 ✓
160.4 EB05 139.5 · IC025 +6.4
3/3 methods agree
Lab value / disease markerserious n=143 · ♀ 100% (drug 58%) · 91% cliniciannot reported in cached trials
Mycobacterium fortuitum infection27177.5
118.0–267.0ROR 177.7 · calibrated p 5e-9 ✓
137.0 EB05 98.9 · IC025 +4.7
3/3 methods agree
Not in label — unassessedserious n=27 · ♀ 0% (drug 58%)not reported in cached trials
Corneal infiltrates44172.9
125.7–237.9ROR 173.3 · calibrated p 3e-9 ✓
139.3 EB05 108.0 · IC025 +5.3
3/3 methods agree
Not in label — unassessedserious n=42 · 100% cliniciannot reported in cached trials
Nasal oedema232154.7
134.9–177.5ROR 156.5 · calibrated p 4e-9 ✓
133.1 EB05 119.3 · IC025 +6.5
3/3 methods agree
Not in label — unassessedserious n=232 · ♀ 100% (drug 58%) · 94% cliniciannot reported in cached trials
Swollen joint count31150.0
102.9–218.6ROR 150.2 · calibrated p 1e-8 ✓
121.3 EB05 89.6 · IC025 +4.8
3/3 methods agree
Not in label — unassessedserious n=31 · ♀ 100% (drug 58%) · 100% cliniciannot reported in cached trials
Keratitis bacterial20148.6
93.0–237.5ROR 148.8 · calibrated p 3e-8 ✓
115.9 EB05 79.2 · IC025 +4.2
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=19 · 100% cliniciannot reported in cached trials
Temperature regulation disorder273148.6
131.0–168.6ROR 150.6 · calibrated p 5e-9 ✓
128.8 EB05 116.5 · IC025 +6.5
3/3 methods agree
Not in label — unassessedserious n=273 · ♀ 100% (drug 58%)not reported in cached trials
Antineutrophil cytoplasmic antibody positive90146.8
117.7–182.9ROR 147.4 · calibrated p 8e-9 ✓
125.1 EB05 104.9 · IC025 +5.9
3/3 methods agree
Lab value / disease markerserious n=90 · ♀ 0% (drug 58%)not reported in cached trials
Grip strength28142.9
96.2–212.1ROR 143.1 · calibrated p 2e-8 ✓
115.8 EB05 84.1 · IC025 +4.7
3/3 methods agree
Not in label — unassessedserious n=28 · ♀ 100% (drug 58%)not reported in cached trials
Anterior chamber fibrin15135.0
78.8–231.2ROR 135.1 · calibrated p 9e-8 ✓
103.9 EB05 66.9 · IC025 +3.8
3/3 methods agree
Not in label — unassessedserious n=15not reported in cached trials
Disseminated mycobacterium avium complex infection22120.0
77.2–186.6ROR 120.2 · calibrated p 1e-7 ✓
98.6 EB05 68.6 · IC025 +4.3
3/3 methods agree
Not in label — unassessedserious n=22 · 100% cliniciannot reported in cached trials
Deep vein thrombosis postoperative202119.5
103.3–138.1ROR 120.7 · calibrated p 3e-8 ✓
106.1 EB05 94.3 · IC025 +6.2
3/3 methods agree
Not in label — unassessedserious n=202 · ♀ 100% (drug 58%) · 91% cliniciannot reported in cached trials
Iris atrophy21117.1
74.5–183.8ROR 117.2 · calibrated p 1e-7 ✓
96.2 EB05 66.4 · IC025 +4.2
3/3 methods agree
Not in label — unassessedserious n=21 · 100% cliniciannot reported in cached trials
Hypopyon83115.3
92.0–144.7ROR 115.8 · calibrated p 5e-8 ✓
101.4 EB05 84.4 · IC025 +5.6
3/3 methods agree
Not in label — unassessedserious n=82 · 94% cliniciannot reported in cached trials
Corneal decompensation15109.1
64.1–185.8ROR 109.2 · calibrated p 4e-7 ✓
88.0 EB05 56.6 · IC025 +3.7
3/3 methods agree
Not in label — unassessedserious n=15not reported in cached trials
Normochromic normocytic anaemia277105.8
93.5–119.6ROR 107.2 · calibrated p 7e-8 ✓
95.4 EB05 86.3 · IC025 +6.2
3/3 methods agree
Not in label — unassessedserious n=277 · ♀ 0% (drug 58%)not reported in cached trials
Neuritis141104.9
88.3–124.7ROR 105.7 · calibrated p 9e-8 ✓
94.1 EB05 81.8 · IC025 +5.9
3/3 methods agree
Not in label — unassessedserious n=141 · ♀ 0% (drug 58%)not reported in cached trials
Corneal epithelium defect52103.6
77.9–137.7ROR 103.8 · calibrated p 1e-7 ✓
91.1 EB05 72.1 · IC025 +5.2
3/3 methods agree
Not in label — unassessedserious n=41not reported in cached trials

Trial evidence (ClinicalTrials.gov)

✓ Trial adverse-event data found on ClinicalTrials.gov

Largest completed trials with posted results that list Moxifloxacin 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).

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.

ReactionReportsPRR 95% CI · ROR · χ²/pEBGM EB05 · IC025Label screenSerious-only & strataTrial cross-check
Off label use (used outside approved label)2,4122.9
2.8–3.0ROR 3.2 · calibrated p 0.578
2.9 EB05 2.8 · IC025 +1.5
3/3 methods agree
Reporting / coding artifactserious PRR 3.3not reported in cached trials
Dyspnoea (shortness of breath)2,2034.1
3.9–4.2ROR 4.4 · calibrated p 0.305
4.0 EB05 3.9 · IC025 +1.9
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 3.7not reported in cached trials
Drug ineffective (drug did not work)2,1051.7
1.6–1.7ROR 1.7 · calibrated p 0.795
1.7 EB05 1.6 · IC025 +0.7Reporting / coding artifactserious PRR 2.9not reported in cached trials
Asthma2,07119.6
18.8–20.4ROR 21.7 · calibrated p 0.001 ✓
19.2 EB05 18.5 · IC025 +4.2
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 18.2 · ♀ 78% (drug 58%)not reported in cached trials
Pneumonia (lung infection)1,9976.5
6.2–6.7ROR 7.1 · calibrated p 0.096
6.4 EB05 6.2 · IC025 +2.6
3/3 methods agree
Likely indication confounding
term in indications
serious PRR 4.5 · ♀ 83% (drug 58%)NCT02563327: 1/825 (0.1%) on Moxifloxacin (serious AE)
Vomiting1,8564.1
4.0–4.3ROR 4.4 · calibrated p 0.304
4.1 EB05 4.0 · IC025 +2.0
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 4.1 · ♀ 89% (drug 58%)NCT02563327: 1/835 (0.1%) on Moxifloxacin (serious AE)
Pain1,7372.9
2.8–3.1ROR 3.1 · calibrated p 0.587
2.9 EB05 2.8 · IC025 +1.5
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 3.0 · ♀ 89% (drug 58%)not reported in cached trials
Wheezing1,66430.1
28.7–31.5ROR 32.7 · calibrated p 2e-4 ✓
29.3 EB05 28.1 · IC025 +4.8
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 27.2not reported in cached trials
Rash1,5493.7
3.6–3.9ROR 4.0 · calibrated p 0.387
3.7 EB05 3.6 · IC025 +1.8
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 5.3 · ♀ 86% (drug 58%)NCT02563327: 1/835 (0.1%) on Moxifloxacin (serious AE)
Fatigue (tiredness)1,4511.9
1.9–2.0ROR 2.0 · calibrated p 0.954
1.9 EB05 1.9 · IC025 +0.9Labeled — boxed warning
synonym match
serious PRR 2.3 · ♀ 80% (drug 58%)not reported in cached trials
Malaise (feeling unwell)1,3043.1
2.9–3.3ROR 3.2 · calibrated p 0.554
3.1 EB05 2.9 · IC025 +1.5
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 3.4 · ♀ 91% (drug 58%)not reported in cached trials
Pyrexia (fever)1,2693.8
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 3.2NCT02563327: 1/846 (0.1%) on Moxifloxacin (serious AE)
Nausea1,2551.7
1.6–1.7ROR 1.7 · calibrated p 0.769
1.7 EB05 1.6 · IC025 +0.6Labeled adverse reaction
exact term
serious PRR 2.0 · ♀ 78% (drug 58%)not reported in cached trials
Condition aggravated1,2224.2
4.0–4.5ROR 4.4 · calibrated p 0.307
4.2 EB05 4.0 · IC025 +2.0
3/3 methods agree
Reporting / coding artifactserious PRR 4.2not reported in cached trials

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.

✓ A hand-written Bradford Hill causality assessment exists for this drug: Oxycodone Hydrochloride ↔ Drug Dependence.

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, asthma, drug hypersensitivity, pneumonia, vomiting, 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.