Fluticasone and Vilanterol side effects: what 35,726 FDA adverse event reports show
Drug class
Inhaled corticosteroid
Label matched
Fluticasone Furoate (Arnuity Ellipta)
Who reports
35,726 reports · 42% serious · 1,466 with death outcome · 66% female
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.
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.
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). 1,125 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 |
|---|---|---|---|---|---|---|
| Right atrial hypertrophy | 73 | 1,139.8 767.5–1,692.5ROR 1,142.1 · calibrated p 7e-17 ✓ | 348.9 EB05 286.7 · IC025 +6.3 3/3 methods agree | Not in label — unassessed | serious n=73 · ♀ 0% (drug 66%) | no trial arm names this drug |
| Inspiratory capacity abnormal | 17 | 892.8 418.2–1,905.9ROR 893.2 · calibrated p 2e-13 ✓ | 252.0 EB05 166.6 · IC025 +4.2 3/3 methods agree | Not in label — unassessed | serious n=17 | no trial arm names this drug |
| Total lung capacity increased | 153 | 755.4 594.0–960.8ROR 758.7 · calibrated p 1e-15 ✓ | 315.0 EB05 275.3 · IC025 +7.0 3/3 methods agree | Not in label — unassessed | serious n=153 · ♀ 100% (drug 66%) | no trial arm names this drug |
| Asthma-chronic obstructive pulmonary disease overlap syndrome | 252 | 555.6 467.5–660.3ROR 559.6 · calibrated p 3e-14 ✓ | 277.7 EB05 250.1 · IC025 +7.3 3/3 methods agree | Not in label — unassessed | serious n=251 | no trial arm names this drug |
| Antacid therapy | 50 | 418.6 290.9–602.3ROR 419.2 · calibrated p 2e-12 ✓ | 222.5 EB05 175.4 · IC025 +5.7 3/3 methods agree | Reporting / coding artifact | serious n=50 · ♀ 33% (drug 66%) · 100% clinician | no trial arm names this drug |
| Salpingo-oophorectomy unilateral | 45 | 406.2 277.5–594.7ROR 406.7 · calibrated p 3e-12 ✓ | 217.0 EB05 168.8 · IC025 +5.6 3/3 methods agree | Not in label — unassessed | serious n=45 · ♀ 100% (drug 66%) · 100% clinician | no trial arm names this drug |
| Expiratory reserve volume decreased | 22 | 310.0 184.7–520.3ROR 310.2 · calibrated p 1e-10 ✓ | 172.1 EB05 119.8 · IC025 +4.5 3/3 methods agree | Lab value / disease marker | serious n=22 · ♀ 0% (drug 66%) | no trial arm names this drug |
| Sleep disorder therapy | 51 | 221.5 160.4–305.9ROR 221.8 · calibrated p 4e-10 ✓ | 151.4 EB05 119.6 · IC025 +5.5 3/3 methods agree | Reporting / coding artifact | serious n=51 · ♀ 0% (drug 66%) · 100% clinician | no trial arm names this drug |
| Fev1/fvc ratio decreased | 28 | 177.7 116.4–271.5ROR 177.9 · calibrated p 5e-9 ✓ | 124.8 EB05 90.6 · IC025 +4.7 3/3 methods agree | Lab value / disease marker | serious n=28 | no trial arm names this drug |
| Appendicolith | 78 | 151.7 118.3–194.6ROR 152.0 · calibrated p 7e-9 ✓ | 117.0 EB05 96.8 · IC025 +5.7 3/3 methods agree | Not in label — unassessed | serious n=78 · ♀ 22% (drug 66%) · 100% clinician | no trial arm names this drug |
| Bronchial wall thickening | 147 | 149.2 124.5–178.9ROR 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 therapy | 62 | 148.6 112.4–196.4ROR 148.9 · calibrated p 9e-9 ✓ | 114.3 EB05 92.4 · IC025 +5.5 3/3 methods agree | Reporting / coding artifact | serious n=62 · ♀ 27% (drug 66%) · 100% clinician | no trial arm names this drug |
| Total lung capacity abnormal | 76 | 146.3 113.8–188.2ROR 146.7 · calibrated p 9e-9 ✓ | 113.7 EB05 93.8 · IC025 +5.7 3/3 methods agree | Not in label — unassessed | serious n=72 · ♀ 0% (drug 66%) | no trial arm names this drug |
| Eosinophil count | 22 | 139.7 87.7–222.5ROR 139.7 · calibrated p 4e-8 ✓ | 102.8 EB05 71.6 · IC025 +4.3 3/3 methods agree | Labeled (related wording) related wording | serious n=21 · ♀ 0% (drug 66%) | no trial arm names this drug |
| Drug therapy | 61 | 138.2 104.5–182.7ROR 138.4 · calibrated p 2e-8 ✓ | 108.0 EB05 87.1 · IC025 +5.5 3/3 methods agree | Reporting / coding artifact | serious n=61 · ♀ 27% (drug 66%) · 100% clinician | no trial arm names this drug |
| Anticoagulant therapy | 51 | 132.1 97.5–179.1ROR 132.3 · calibrated p 3e-8 ✓ | 103.6 EB05 81.9 · IC025 +5.3 3/3 methods agree | Reporting / coding artifact | serious n=51 · ♀ 33% (drug 66%) · 100% clinician | no trial arm names this drug |
| Capillaritis | 48 | 127.8 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 — unassessed | serious n=48 · ♀ 0% (drug 66%) · 100% clinician | no trial arm names this drug |
| Congenital hiatus hernia | 30 | 91.7 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 — unassessed | serious n=30 · ♀ 0% (drug 66%) · 100% clinician | no trial arm names this drug |
| Eosinophilic bronchitis | 27 | 90.2 60.1–135.2ROR 90.2 · calibrated p 7e-7 ✓ | 74.2 EB05 53.5 · IC025 +4.4 3/3 methods agree | Labeled (related wording) related wording | serious n=27 · ♀ 0% (drug 66%) | no trial arm names this drug |
| Mite allergy | 85 | 90.1 71.7–113.2ROR 90.3 · calibrated p 3e-7 ✓ | 76.8 EB05 64.0 · IC025 +5.4 3/3 methods agree | Labeled (related wording) related wording | serious n=85 · ♀ 15% (drug 66%) | no trial arm names this drug |
| Dust allergy | 128 | 89.7 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 — unassessed | serious n=128 · ♀ 19% (drug 66%) | no trial arm names this drug |
| Pulmonary vasculitis | 67 | 85.1 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 — unassessed | serious n=67 · ♀ 0% (drug 66%) · 100% clinician | no trial arm names this drug |
| Lung diffusion disorder | 20 | 85.0 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 — unassessed | serious n=20 | no trial arm names this drug |
| Respiratory gas exchange disorder | 45 | 81.0 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 — unassessed | serious n=45 | no trial arm names this drug |
| Spirometry abnormal | 69 | 78.0 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 marker | serious n=67 · ♀ 0% (drug 66%) · 100% clinician | no trial arm names this drug |
| Prolonged expiration | 31 | 77.9 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 — unassessed | serious n=31 · ♀ 0% (drug 66%) | no trial arm names this drug |
| Malignant melanoma stage 0 | 21 | 76.8 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 — unassessed | serious n=21 · 100% clinician | no trial arm names this drug |
| Bacteroides infection | 30 | 76.7 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 — unassessed | serious n=30 · ♀ 0% (drug 66%) · 100% clinician | no trial arm names this drug |
| Sputum purulent | 73 | 72.6 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 — unassessed | serious n=73 | no trial arm names this drug |
| Eosinophilic pneumonia chronic | 32 | 69.8 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 — unassessed | serious n=32 · ♀ 0% (drug 66%) · 75% consumer | no trial arm names this drug |
| Product confusion | 79 | 66.3 52.6–83.7ROR 66.5 · calibrated p 3e-6 ✓ | 58.8 EB05 48.7 · IC025 +5.1 3/3 methods agree | Reporting / coding artifact | 90% consumer | no trial arm names this drug |
| Pulmonary function test abnormal | 158 | 65.9 56.0–77.7ROR 66.2 · calibrated p 2e-6 ✓ | 58.9 EB05 51.6 · IC025 +5.4 3/3 methods agree | Reporting / coding artifact | serious n=156 · ♀ 18% (drug 66%) | no trial arm names this drug |
| Vital capacity decreased | 44 | 63.4 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 — unassessed | serious n=44 · ♀ 0% (drug 66%) | no trial arm names this drug |
| Obstructive airways disorder | 1,058 | 61.4 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 — unassessed | serious PRR 79.1 | no trial arm names this drug |
| Lung hyperinflation | 77 | 57.3 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 — unassessed | serious n=74 · ♀ 42% (drug 66%) | no trial arm names this drug |
| Mycotic allergy | 73 | 55.6 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 — unassessed | serious n=73 · ♀ 0% (drug 66%) · 100% clinician | no trial arm names this drug |
| Venous pressure jugular increased | 31 | 53.9 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 — unassessed | serious n=31 · ♀ 100% (drug 66%) | no trial arm names this drug |
| Lymph node calcification | 16 | 52.2 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 — unassessed | serious n=16 | no trial arm names this drug |
| Right ventricular hypertrophy | 73 | 51.1 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 — unassessed | serious n=73 · ♀ 0% (drug 66%) | no trial arm names this drug |
| Bronchial obstruction | 107 | 48.2 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)
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 |
|---|---|---|---|---|---|---|
| Dyspnoea (shortness of breath) | 6,164 | 6.5 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 — unassessed | serious PRR 7.3 · 72% consumer | no trial arm names this drug |
| Drug ineffective (drug did not work) | 4,032 | 1.8 1.7–1.9ROR 1.9 · calibrated p 0.888 | 1.8 EB05 1.7 · IC025 +0.8 | Reporting / coding artifact | serious PRR 2.3 · 80% consumer | no trial arm names this drug |
| Asthma | 4,000 | 21.7 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 34.3 | no trial arm names this drug |
| Cough | 3,425 | 7.3 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 10.5 | no trial arm names this drug |
| Wheezing | 2,666 | 27.6 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 — unassessed | serious PRR 42.4 | no trial arm names this drug |
| Wrong technique in device usage process | 2,298 | 31.0 29.8–32.3ROR 33.1 · calibrated p 2e-4 ✓ | 29.5 EB05 28.5 · IC025 +4.8 3/3 methods agree | Reporting / coding artifact | serious n=120 · 96% consumer | no trial arm names this drug |
| Pneumonia (lung infection) | 2,199 | 4.0 3.9–4.2ROR 4.2 · calibrated p 0.341 | 4.0 EB05 3.8 · IC025 +1.9 3/3 methods agree | Labeled (related wording) related wording | serious PRR 5.7 | no trial arm names this drug |
| Product complaint | 1,843 | 46.7 44.6–48.9ROR 49.2 · calibrated p 1e-5 ✓ | 43.3 EB05 41.7 · IC025 +5.3 3/3 methods agree | Reporting / coding artifact | serious n=113 · 93% consumer | no trial arm names this drug |
| Product dose omission issue | 1,789 | 3.7 3.5–3.9ROR 3.8 · calibrated p 0.408 | 3.7 EB05 3.5 · IC025 +1.8 3/3 methods agree | Reporting / coding artifact | serious PRR 5.6 · 79% consumer | no trial arm names this drug |
| Fatigue (tiredness) | 1,744 | 1.3 1.3–1.4ROR 1.3 · calibrated p 0.531 | 1.3 EB05 1.3 · IC025 +0.3 | Labeled adverse reaction exact term | serious PRR 2.3 | no trial arm names this drug |
| Off label use (used outside approved label) | 1,551 | 1.0 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 artifact | serious PRR 1.2 | no trial arm names this drug |
| Therapeutic product effect incomplete | 1,541 | 13.0 12.4–13.7ROR 13.6 · calibrated p 0.010 ✓ | 12.8 EB05 12.2 · IC025 +3.6 3/3 methods agree | Reporting / coding artifact | serious PRR 31.7 | no trial arm names this drug |
| Malaise (feeling unwell) | 1,465 | 2.0 1.9–2.1ROR 2.0 · calibrated p 0.943 | 2.0 EB05 1.9 · IC025 +0.9 | Not in label — unassessed | serious PRR 2.9 | no trial arm names this drug |
| Loss of personal independence in daily activities | 1,388 | 17.6 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 — unassessed | serious PRR 30.4 | no trial arm names this drug |
| Headache | 1,336 | 1.3 1.2–1.3ROR 1.3 · calibrated p 0.482 | 1.3 EB05 1.2 · IC025 +0.2 | Labeled adverse reaction exact term | serious PRR 1.8 | 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.
- Right atrial hypertrophy — n=73, PRR 1,139.8
- Total lung capacity increased — n=153, PRR 755.4
- Asthma-chronic obstructive pulmonary disease overlap syndrome — n=252, PRR 555.6
- Salpingo-oophorectomy unilateral — n=45, PRR 406.2
- Appendicolith — n=78, PRR 151.7
- Total lung capacity abnormal — n=76, PRR 146.3
- Capillaritis — n=48, PRR 127.8
- Congenital hiatus hernia — n=30, PRR 91.7
- Dust allergy — n=128, PRR 89.7
- Pulmonary vasculitis — n=67, PRR 85.1
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
- FDA label via openFDA (set ID 50f193ee-1691-486d-9370-a664df63695c, effective 20231018; matched on
openfda.generic_name.exact:"FLUTICASONE FUROATE") - 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, 1,165 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
FLUTICASONE FUROATE, 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.