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Fluticasone and Vilanterol side effects: what 35,726 FDA adverse event reports show

Fluticasone Furoate And Vilanterol Trifenatate · 1,165 reaction terms · 157,982 drug–reaction co-reports · data 2026-09-14
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Drug class

Inhaled corticosteroid

FDA label, Indications wording of the closest related product

Label matched

Fluticasone Furoate (Arnuity Ellipta)

closest FDA label found for this product string; brand list suppressed because the label is a related product, not an exact match

Who reports

35,726 reports · 42% serious · 1,466 with death outcome · 66% female

openFDA FAERS counts, all years, deduplication not applied

Used for

ARNUITY ELLIPTA is indicated for the maintenance treatment of asthma in adult and pediatric patients aged 5 years and older. Limitations of Use ARNUITY ELLIPTA is NOT indicated for the relief of acute bronchospasm. ARNUITY ELLIPTA is an inhaled corticosteroid indicated for the maintenance treatment of asthma in adult and pediatric patients aged 5 years and older.

FDA label, Indications and Usage

What it is

ARNUITY ELLIPTA is an inhalation powder drug product for delivery of fluticasone furoate (an ICS) to patients by oral inhalation. Fluticasone furoate, a synthetic trifluorinated corticosteroid.

FDA label, Description section

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) 3Likely indication confounding 2Reporting / coding artifact 7Lab value / disease marker 3Not in label — unassessed 25
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). 1,125 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
Right atrial hypertrophy731,139.8
767.5–1,692.5ROR 1,142.1 · calibrated p 7e-17 ✓
348.9 EB05 286.7 · IC025 +6.3
3/3 methods agree
Not in label — unassessedserious n=73 · ♀ 0% (drug 66%)no trial arm names this drug
Inspiratory capacity abnormal17892.8
418.2–1,905.9ROR 893.2 · calibrated p 2e-13 ✓
252.0 EB05 166.6 · IC025 +4.2
3/3 methods agree
Not in label — unassessedserious n=17no trial arm names this drug
Total lung capacity increased153755.4
594.0–960.8ROR 758.7 · calibrated p 1e-15 ✓
315.0 EB05 275.3 · IC025 +7.0
3/3 methods agree
Not in label — unassessedserious n=153 · ♀ 100% (drug 66%)no trial arm names this drug
Asthma-chronic obstructive pulmonary disease overlap syndrome252555.6
467.5–660.3ROR 559.6 · calibrated p 3e-14 ✓
277.7 EB05 250.1 · IC025 +7.3
3/3 methods agree
Not in label — unassessedserious n=251no trial arm names this drug
Antacid therapy50418.6
290.9–602.3ROR 419.2 · calibrated p 2e-12 ✓
222.5 EB05 175.4 · IC025 +5.7
3/3 methods agree
Reporting / coding artifactserious n=50 · ♀ 33% (drug 66%) · 100% clinicianno trial arm names this drug
Salpingo-oophorectomy unilateral45406.2
277.5–594.7ROR 406.7 · calibrated p 3e-12 ✓
217.0 EB05 168.8 · IC025 +5.6
3/3 methods agree
Not in label — unassessedserious n=45 · ♀ 100% (drug 66%) · 100% clinicianno trial arm names this drug
Expiratory reserve volume decreased22310.0
184.7–520.3ROR 310.2 · calibrated p 1e-10 ✓
172.1 EB05 119.8 · IC025 +4.5
3/3 methods agree
Lab value / disease markerserious n=22 · ♀ 0% (drug 66%)no trial arm names this drug
Sleep disorder therapy51221.5
160.4–305.9ROR 221.8 · calibrated p 4e-10 ✓
151.4 EB05 119.6 · IC025 +5.5
3/3 methods agree
Reporting / coding artifactserious n=51 · ♀ 0% (drug 66%) · 100% clinicianno trial arm names this drug
Fev1/fvc ratio decreased28177.7
116.4–271.5ROR 177.9 · calibrated p 5e-9 ✓
124.8 EB05 90.6 · IC025 +4.7
3/3 methods agree
Lab value / disease markerserious n=28no trial arm names this drug
Appendicolith78151.7
118.3–194.6ROR 152.0 · calibrated p 7e-9 ✓
117.0 EB05 96.8 · IC025 +5.7
3/3 methods agree
Not in label — unassessedserious n=78 · ♀ 22% (drug 66%) · 100% clinicianno trial arm names this drug
Bronchial wall thickening147149.2
124.5–178.9ROR 149.9 · calibrated p 6e-9 ✓
117.0 EB05 102.0 · IC025 +6.1
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=147 · ♀ 26% (drug 66%)no trial arm names this drug
Analgesic therapy62148.6
112.4–196.4ROR 148.9 · calibrated p 9e-9 ✓
114.3 EB05 92.4 · IC025 +5.5
3/3 methods agree
Reporting / coding artifactserious n=62 · ♀ 27% (drug 66%) · 100% clinicianno trial arm names this drug
Total lung capacity abnormal76146.3
113.8–188.2ROR 146.7 · calibrated p 9e-9 ✓
113.7 EB05 93.8 · IC025 +5.7
3/3 methods agree
Not in label — unassessedserious n=72 · ♀ 0% (drug 66%)no trial arm names this drug
Drug therapy61138.2
104.5–182.7ROR 138.4 · calibrated p 2e-8 ✓
108.0 EB05 87.1 · IC025 +5.5
3/3 methods agree
Reporting / coding artifactserious n=61 · ♀ 27% (drug 66%) · 100% clinicianno trial arm names this drug
Anticoagulant therapy51132.1
97.5–179.1ROR 132.3 · calibrated p 3e-8 ✓
103.6 EB05 81.9 · IC025 +5.3
3/3 methods agree
Reporting / coding artifactserious n=51 · ♀ 33% (drug 66%) · 100% clinicianno trial arm names this drug
Capillaritis48127.8
93.5–174.7ROR 128.0 · calibrated p 3e-8 ✓
100.7 EB05 79.0 · IC025 +5.2
3/3 methods agree
Not in label — unassessedserious n=48 · ♀ 0% (drug 66%) · 100% clinicianno trial arm names this drug
Congenital hiatus hernia3091.7
62.4–134.8ROR 91.8 · calibrated p 5e-7 ✓
75.6 EB05 55.5 · IC025 +4.5
3/3 methods agree
Not in label — unassessedserious n=30 · ♀ 0% (drug 66%) · 100% clinicianno trial arm names this drug
Dust allergy12889.7
74.5–108.1ROR 90.1 · calibrated p 3e-7 ✓
76.9 EB05 66.4 · IC025 +5.6
3/3 methods agree
Not in label — unassessedserious n=128 · ♀ 19% (drug 66%)no trial arm names this drug
Pulmonary vasculitis6785.1
65.8–109.9ROR 85.2 · calibrated p 6e-7 ✓
72.8 EB05 59.3 · IC025 +5.2
3/3 methods agree
Not in label — unassessedserious n=67 · ♀ 0% (drug 66%) · 100% clinicianno trial arm names this drug
Lung diffusion disorder2085.0
53.1–135.8ROR 85.0 · calibrated p 1e-6 ✓
69.5 EB05 47.5 · IC025 +4.0
3/3 methods agree
Not in label — unassessedserious n=20no trial arm names this drug
Respiratory gas exchange disorder4581.0
59.3–110.6ROR 81.1 · calibrated p 9e-7 ✓
69.1 EB05 53.8 · IC025 +4.8
3/3 methods agree
Not in label — unassessedserious n=45no trial arm names this drug
Spirometry abnormal6978.0
60.7–100.3ROR 78.2 · calibrated p 1e-6 ✓
67.6 EB05 55.2 · IC025 +5.1
3/3 methods agree
Lab value / disease markerserious n=67 · ♀ 0% (drug 66%) · 100% clinicianno trial arm names this drug
Prolonged expiration3177.9
53.5–113.3ROR 77.9 · calibrated p 2e-6 ✓
66.1 EB05 48.8 · IC025 +4.5
3/3 methods agree
Not in label — unassessedserious n=31 · ♀ 0% (drug 66%)no trial arm names this drug
Malignant melanoma stage 02176.8
48.7–121.0ROR 76.8 · calibrated p 2e-6 ✓
64.1 EB05 44.2 · IC025 +4.0
3/3 methods agree
Not in label — unassessedserious n=21 · 100% clinicianno trial arm names this drug
Bacteroides infection3076.7
52.4–112.2ROR 76.7 · calibrated p 2e-6 ✓
65.1 EB05 47.8 · IC025 +4.4
3/3 methods agree
Not in label — unassessedserious n=30 · ♀ 0% (drug 66%) · 100% clinicianno trial arm names this drug
Sputum purulent7372.6
56.9–92.6ROR 72.7 · calibrated p 2e-6 ✓
63.6 EB05 52.2 · IC025 +5.1
3/3 methods agree
Not in label — unassessedserious n=73no trial arm names this drug
Eosinophilic pneumonia chronic3269.8
48.3–100.7ROR 69.8 · calibrated p 3e-6 ✓
60.2 EB05 44.7 · IC025 +4.4
3/3 methods agree
Not in label — unassessedserious n=32 · ♀ 0% (drug 66%) · 75% consumerno trial arm names this drug
Product confusion7966.3
52.6–83.7ROR 66.5 · calibrated p 3e-6 ✓
58.8 EB05 48.7 · IC025 +5.1
3/3 methods agree
Reporting / coding artifact90% consumerno trial arm names this drug
Pulmonary function test abnormal15865.9
56.0–77.7ROR 66.2 · calibrated p 2e-6 ✓
58.9 EB05 51.6 · IC025 +5.4
3/3 methods agree
Reporting / coding artifactserious n=156 · ♀ 18% (drug 66%)no trial arm names this drug
Vital capacity decreased4463.4
46.4–86.5ROR 63.5 · calibrated p 5e-6 ✓
55.9 EB05 43.4 · IC025 +4.6
3/3 methods agree
Not in label — unassessedserious n=44 · ♀ 0% (drug 66%)no trial arm names this drug
Obstructive airways disorder1,05861.4
57.7–65.3ROR 63.2 · calibrated p 3e-6 ✓
55.5 EB05 52.8 · IC025 +5.7
3/3 methods agree
Not in label — unassessedserious PRR 79.1no trial arm names this drug
Lung hyperinflation7757.3
45.4–72.4ROR 57.4 · calibrated p 7e-6 ✓
51.6 EB05 42.6 · IC025 +4.9
3/3 methods agree
Not in label — unassessedserious n=74 · ♀ 42% (drug 66%)no trial arm names this drug
Mycotic allergy7355.6
43.7–70.6ROR 55.7 · calibrated p 9e-6 ✓
50.1 EB05 41.2 · IC025 +4.9
3/3 methods agree
Not in label — unassessedserious n=73 · ♀ 0% (drug 66%) · 100% clinicianno trial arm names this drug
Venous pressure jugular increased3153.9
37.3–77.9ROR 54.0 · calibrated p 2e-5 ✓
48.1 EB05 35.5 · IC025 +4.2
3/3 methods agree
Not in label — unassessedserious n=31 · ♀ 100% (drug 66%)no trial arm names this drug
Lymph node calcification1652.2
31.3–87.1ROR 52.2 · calibrated p 3e-5 ✓
45.6 EB05 29.7 · IC025 +3.5
3/3 methods agree
Not in label — unassessedserious n=16no trial arm names this drug
Right ventricular hypertrophy7351.1
40.2–64.8ROR 51.2 · calibrated p 2e-5 ✓
46.5 EB05 38.2 · IC025 +4.8
3/3 methods agree
Not in label — unassessedserious n=73 · ♀ 0% (drug 66%)no trial arm names this drug
Bronchial obstruction10748.2
39.6–58.7ROR 48.4 · calibrated p 2e-5 ✓
44.3 EB05 37.7 · IC025 +4.9
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=107 · ♀ 44% (drug 66%)no trial arm names this drug

Trial evidence (ClinicalTrials.gov)

No completed trial with posted adverse-event results was found on ClinicalTrials.gov for Fluticasone and Vilanterol (searched FLUTICASONE FUROATE).

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
Dyspnoea (shortness of breath)6,1646.5
6.3–6.6ROR 7.6 · calibrated p 0.078
6.4 EB05 6.3 · IC025 +2.6
3/3 methods agree
Not in label — unassessedserious PRR 7.3 · 72% consumerno trial arm names this drug
Drug ineffective (drug did not work)4,0321.8
1.7–1.9ROR 1.9 · calibrated p 0.888
1.8 EB05 1.7 · IC025 +0.8Reporting / coding artifactserious PRR 2.3 · 80% consumerno trial arm names this drug
Asthma4,00021.7
21.0–22.3ROR 24.3 · calibrated p 8e-4 ✓
20.9 EB05 20.4 · IC025 +4.3
3/3 methods agree
Likely indication confounding
term in indications; also in warnings
serious PRR 34.3no trial arm names this drug
Cough3,4257.3
7.0–7.5ROR 7.9 · calibrated p 0.069
7.2 EB05 7.0 · IC025 +2.8
3/3 methods agree
Labeled adverse reaction
exact term
serious PRR 10.5no trial arm names this drug
Wheezing2,66627.6
26.6–28.7ROR 29.8 · calibrated p 3e-4 ✓
26.4 EB05 25.6 · IC025 +4.7
3/3 methods agree
Not in label — unassessedserious PRR 42.4no trial arm names this drug
Wrong technique in device usage process2,29831.0
29.8–32.3ROR 33.1 · calibrated p 2e-4 ✓
29.5 EB05 28.5 · IC025 +4.8
3/3 methods agree
Reporting / coding artifactserious n=120 · 96% consumerno trial arm names this drug
Product complaint1,84346.7
44.6–48.9ROR 49.2 · calibrated p 1e-5 ✓
43.3 EB05 41.7 · IC025 +5.3
3/3 methods agree
Reporting / coding artifactserious n=113 · 93% consumerno trial arm names this drug
Product dose omission issue1,7893.7
3.5–3.9ROR 3.8 · calibrated p 0.408
3.7 EB05 3.5 · IC025 +1.8
3/3 methods agree
Reporting / coding artifactserious PRR 5.6 · 79% consumerno trial arm names this drug
Fatigue (tiredness)1,7441.3
1.3–1.4ROR 1.3 · calibrated p 0.531
1.3 EB05 1.3 · IC025 +0.3Labeled adverse reaction
exact term
serious PRR 2.3no trial arm names this drug
Off label use (used outside approved label)1,5511.0
1.0–1.1ROR 1.1 · calibrated p 0.340
1.0 EB05 1.0 · IC025 -0.0
PRR-only: not supported by EBGM or IC
Reporting / coding artifactserious PRR 1.2no trial arm names this drug
Therapeutic product effect incomplete1,54113.0
12.4–13.7ROR 13.6 · calibrated p 0.010 ✓
12.8 EB05 12.2 · IC025 +3.6
3/3 methods agree
Reporting / coding artifactserious PRR 31.7no trial arm names this drug
Malaise (feeling unwell)1,4652.0
1.9–2.1ROR 2.0 · calibrated p 0.943
2.0 EB05 1.9 · IC025 +0.9Not in label — unassessedserious PRR 2.9no trial arm names this drug
Loss of personal independence in daily activities1,38817.6
16.7–18.6ROR 18.3 · calibrated p 0.003 ✓
17.1 EB05 16.4 · IC025 +4.0
3/3 methods agree
Not in label — unassessedserious PRR 30.4no trial arm names this drug
Headache1,3361.3
1.2–1.3ROR 1.3 · calibrated p 0.482
1.3 EB05 1.2 · IC025 +0.2Labeled adverse reaction
exact term
serious PRR 1.8no 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 Fluticasone and Vilanterol?

In FDA FAERS, the most frequently co-reported reaction terms for Fluticasone and Vilanterol are dyspnoea, asthma, cough, wheezing, pneumonia, fatigue. 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 Fluticasone and Vilanterol have an FDA boxed warning?

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

Do FAERS signals prove that Fluticasone and Vilanterol 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.