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Drug · FAERS side-effect profile with label screen

Mepolizumab side effects: what 49,291 FDA adverse event reports show

Mepolizumab · Nucala · 1,202 reaction terms · 321,903 drug–reaction co-reports · data 2026-09-14
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Drug class

Interleukin-5 Antagonist

FDA label (Established Pharmacologic Class)

Brand names

Nucala

openFDA label

Who reports

49,291 reports · 63% serious · 3,989 with death outcome · 68% female

openFDA FAERS counts, all years, deduplication not applied

Used for

NUCALA is an interleukin-5 (IL-5) antagonist monoclonal antibody (IgG1 kappa) indicated for: • Add-on maintenance treatment of adult and pediatric patients aged 6 years and older with severe asthma and with an eosinophilic phenotype. ( 1.1 ) • Add-on maintenance treatment of adult patients aged 18 years and older with chronic rhinosinusitis with nasal polyps (CRSwNP).

FDA label, Indications and Usage

What it is

Mepolizumab is a humanized IL-5 antagonist monoclonal antibody. Mepolizumab is produced by recombinant DNA technology in Chinese hamster ovary cells. Mepolizumab has a molecular weight of approximately 149 kDa.

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) 2Likely indication confounding 7Reporting / coding artifact 3Lab value / disease marker 4Not in label — unassessed 24
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). 1,162 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
Plethysmography2510,447.2
1,415.6–77,102.2ROR 10,452.5 · calibrated p 1e-11 ✓
307.9 EB05 219.3 · IC025 +4.8
3/3 methods agree
Not in label — unassessedserious n=25 · ♀ 100% (drug 68%) · 100% consumernot reported in cached trials
Total lung capacity increased186925.3
715.3–1,197.1ROR 928.8 · calibrated p 2e-16 ✓
280.3 EB05 248.0 · IC025 +7.1
3/3 methods agree
Not in label — unassessedserious n=185 · ♀ 94% (drug 68%)not reported in cached trials
Sputum culture25870.6
437.4–1,732.7ROR 871.0 · calibrated p 9e-14 ✓
232.8 EB05 165.8 · IC025 +4.8
3/3 methods agree
Lab value / disease markerserious n=25not reported in cached trials
Heart sounds63797.8
523.6–1,215.5ROR 798.8 · calibrated p 5e-15 ✓
253.8 EB05 205.4 · IC025 +6.0
3/3 methods agree
Not in label — unassessedserious n=63 · ♀ 100% (drug 68%)not reported in cached trials
Airway remodelling68516.7
362.1–737.1ROR 517.4 · calibrated p 2e-13 ✓
217.5 EB05 177.4 · IC025 +6.0
3/3 methods agree
Not in label — unassessedserious n=68 · ♀ 33% (drug 68%)not reported in cached trials
Hepatic enzyme73469.3
336.0–655.5ROR 470.0 · calibrated p 5e-13 ✓
209.5 EB05 172.2 · IC025 +6.1
3/3 methods agree
Not in label — unassessedserious n=73 · ♀ 100% (drug 68%) · 100% cliniciannot reported in cached trials
Reversible airways obstruction226334.9
281.2–398.9ROR 336.4 · calibrated p 4e-12 ✓
183.5 EB05 164.3 · IC025 +6.8
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=226not reported in cached trials
Vital capacity decreased184294.6
244.0–355.7ROR 295.7 · calibrated p 2e-11 ✓
170.2 EB05 150.5 · IC025 +6.6
3/3 methods agree
Not in label — unassessedserious n=184not reported in cached trials
Total lung capacity abnormal146265.3
215.6–326.3ROR 266.1 · calibrated p 5e-11 ✓
159.3 EB05 138.8 · IC025 +6.4
3/3 methods agree
Not in label — unassessedserious n=145 · ♀ 0% (drug 68%)not reported in cached trials
Prolonged expiration100259.6
202.3–333.1ROR 260.1 · calibrated p 7e-11 ✓
155.8 EB05 131.8 · IC025 +6.2
3/3 methods agree
Not in label — unassessedserious n=100not reported in cached trials
Hypocholesterolaemia109233.6
184.8–295.2ROR 234.1 · calibrated p 2e-10 ✓
146.4 EB05 124.7 · IC025 +6.2
3/3 methods agree
Not in label — unassessedserious n=109 · ♀ 100% (drug 68%) · 100% cliniciannot reported in cached trials
Pulmonary vasculitis177214.4
178.9–256.9ROR 215.2 · calibrated p 3e-10 ✓
139.9 EB05 123.5 · IC025 +6.4
3/3 methods agree
Not in label — unassessedserious n=177 · ♀ 0% (drug 68%)not reported in cached trials
Eosinophilic granulomatosis with polyangiitis671212.1
193.4–232.7ROR 215.0 · calibrated p 2e-10 ✓
140.5 EB05 131.8 · IC025 +6.9
3/3 methods agree
Likely indication confounding
term in indications; also in warnings
serious n=671 · ♀ 29% (drug 68%)not reported in cached trials
Eosinophil count abnormal227186.4
159.4–217.9ROR 187.2 · calibrated p 9e-10 ✓
127.8 EB05 114.5 · IC025 +6.4
3/3 methods agree
Likely indication confounding
term in indications; also in warnings
serious n=217not reported in cached trials
Central nervous system mass27173.6
110.8–271.9ROR 173.7 · calibrated p 7e-9 ✓
113.3 EB05 81.8 · IC025 +4.6
3/3 methods agree
Not in label — unassessedserious n=27 · ♀ 0% (drug 68%) · 100% cliniciannot reported in cached trials
Bronchopulmonary aspergillosis allergic262170.3
147.5–196.5ROR 171.2 · calibrated p 2e-9 ✓
120.2 EB05 108.5 · IC025 +6.4
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=262not reported in cached trials
Spirometry abnormal163163.3
136.3–195.7ROR 163.9 · calibrated p 3e-9 ✓
116.1 EB05 101.9 · IC025 +6.2
3/3 methods agree
Lab value / disease markerserious n=162 · ♀ 10% (drug 68%)not reported in cached trials
Capillaritis67141.4
107.2–186.5ROR 141.6 · calibrated p 1e-8 ✓
102.9 EB05 83.8 · IC025 +5.5
3/3 methods agree
Not in label — unassessedserious n=67 · ♀ 0% (drug 68%)not reported in cached trials
Wall motion score index abnormal27137.6
89.1–212.5ROR 137.7 · calibrated p 4e-8 ✓
96.8 EB05 69.9 · IC025 +4.5
3/3 methods agree
Lab value / disease markerserious n=27 · ♀ 0% (drug 68%) · 100% cliniciannot reported in cached trials
Antacid therapy29134.7
88.6–204.6ROR 134.7 · calibrated p 4e-8 ✓
95.8 EB05 70.0 · IC025 +4.6
3/3 methods agree
Reporting / coding artifactserious n=29 · ♀ 0% (drug 68%) · 100% cliniciannot reported in cached trials
Lung diffusion disorder38134.6
93.4–193.9ROR 134.7 · calibrated p 3e-8 ✓
97.2 EB05 73.9 · IC025 +4.9
3/3 methods agree
Not in label — unassessedserious n=38 · ♀ 42% (drug 68%)not reported in cached trials
Mite allergy153134.0
111.7–160.8ROR 134.5 · calibrated p 1e-8 ✓
100.5 EB05 87.8 · IC025 +6.0
3/3 methods agree
Not in label — unassessedserious n=153 · ♀ 14% (drug 68%)not reported in cached trials
Fungal disease carrier24132.0
83.4–208.8ROR 132.0 · calibrated p 6e-8 ✓
93.3 EB05 66.0 · IC025 +4.4
3/3 methods agree
Reporting / coding artifactserious n=24not reported in cached trials
Acquired factor v deficiency26129.3
83.3–200.8ROR 129.4 · calibrated p 6e-8 ✓
92.5 EB05 66.3 · IC025 +4.5
3/3 methods agree
Not in label — unassessedserious n=26 · ♀ 0% (drug 68%)not reported in cached trials
Coagulation factor v level abnormal29128.9
85.0–195.5ROR 129.0 · calibrated p 6e-8 ✓
92.9 EB05 67.8 · IC025 +4.6
3/3 methods agree
Lab value / disease markerserious n=29 · ♀ 0% (drug 68%)not reported in cached trials
Facet joint syndrome723126.5
116.4–137.4ROR 128.3 · calibrated p 2e-8 ✓
97.1 EB05 91.3 · IC025 +6.4
3/3 methods agree
Not in label — unassessedserious n=723 · ♀ 100% (drug 68%) · 93% cliniciannot reported in cached trials
Respiratory gas exchange disorder79115.0
89.7–147.5ROR 115.2 · calibrated p 6e-8 ✓
88.5 EB05 73.3 · IC025 +5.5
3/3 methods agree
Not in label — unassessedserious n=79not reported in cached trials
Nasal polypectomy31108.0
72.7–160.2ROR 108.0 · calibrated p 2e-7 ✓
81.8 EB05 60.4 · IC025 +4.6
3/3 methods agree
Not in label — unassessedserious n=27 · 100% consumernot reported in cached trials
Obstructive airways disorder2,175102.8
98.2–107.7ROR 107.5 · calibrated p 7e-8 ✓
82.6 EB05 79.8 · IC025 +6.3
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
age-adj. PRR 143.7 · serious PRR 78.2NCT02105948: 1/184 (0.5%) on Mepolizumab; 1/229 (0.4%) control (serious AE)
Vocal cord dysfunction97102.4
82.0–127.8ROR 102.6 · calibrated p 1e-7 ✓
81.1 EB05 68.5 · IC025 +5.5
3/3 methods agree
Not in label — unassessedserious n=96 · ♀ 93% (drug 68%)not reported in cached trials
Sleep disorder due to a general medical condition3,118101.5
97.7–105.4ROR 108.2 · calibrated p 6e-8 ✓
81.8 EB05 79.4 · IC025 +6.3
3/3 methods agree
Not in label — unassessedage-adj. PRR 118.9 · serious PRR 147.4not reported in cached trials
Bronchial wall thickening13698.0
81.3–118.1ROR 98.3 · calibrated p 2e-7 ✓
78.7 EB05 68.2 · IC025 +5.7
3/3 methods agree
Likely indication confounding
shares a disease stem with the indications wording
serious n=136not reported in cached trials
Pulmonary function test abnormal29096.8
85.2–109.9ROR 97.4 · calibrated p 2e-7 ✓
78.4 EB05 71.1 · IC025 +5.9
3/3 methods agree
Reporting / coding artifactserious n=289not reported in cached trials
Malignant melanoma stage 03394.5
64.7–137.8ROR 94.5 · calibrated p 4e-7 ✓
74.0 EB05 55.2 · IC025 +4.6
3/3 methods agree
Not in label — unassessedserious n=33 · ♀ 0% (drug 68%) · 100% cliniciannot reported in cached trials
Congenital hiatus hernia4093.4
66.3–131.5ROR 93.5 · calibrated p 4e-7 ✓
73.9 EB05 56.6 · IC025 +4.8
3/3 methods agree
Not in label — unassessedserious n=40 · ♀ 0% (drug 68%) · 100% cliniciannot reported in cached trials
Coagulation factor deficiency2992.5
61.9–138.3ROR 92.6 · calibrated p 6e-7 ✓
72.4 EB05 52.9 · IC025 +4.4
3/3 methods agree
Not in label — unassessedserious n=29 · ♀ 0% (drug 68%)not reported in cached trials
Laryngeal stenosis10291.1
73.5–112.8ROR 91.3 · calibrated p 3e-7 ✓
74.0 EB05 62.7 · IC025 +5.5
3/3 methods agree
Not in label — unassessedserious n=102 · ♀ 100% (drug 68%) · 72% consumernot reported in cached trials
Nasal polyps84990.7
84.2–97.6ROR 92.2 · calibrated p 2e-7 ✓
74.6 EB05 70.4 · IC025 +6.0
3/3 methods agree
Likely indication confounding
term in indications; also in warnings
serious n=770not reported in cached trials

Clinical concept groups

MedDRA splits one clinical problem across several terms (e.g. "neutropenia", "neutrophil count decreased", "agranulocytosis"), which dilutes term-level signals. These rows count reports with any term in a concept group (an exact union, not a sum), compared with all other drugs. Groups are hand-built and listed in the methods.

ConceptReportsPRR 95% CIReading
Interstitial lung disease7633.43.2–3.6signal
Serious infection5,9003.33.2–3.3signal
Opportunistic infection6091.91.8–2.1raised
Liver injury1,3431.91.8–2.0raised
Depression1,2501.91.8–2.0raised
Hyperglycaemia / diabetes1,5111.91.8–2.0raised
Fall / fracture1,5091.71.6–1.8raised
Anaphylaxis / angioedema3491.21.1–1.3raised
Venous thromboembolism5951.21.1–1.3raised
Arrhythmia / qt5221.11.1–1.2raised
Heart failure3960.90.9–1.0no difference
Malignancy8060.90.8–1.0lower than other drugs
Pancreatitis1680.90.8–1.0no difference
Tendon disorder730.80.6–1.0no difference
Myocardial infarction3830.80.7–0.9lower than other drugs
Stroke3770.60.6–0.7lower than other drugs

Trial evidence (ClinicalTrials.gov)

✓ Trial adverse-event data found on ClinicalTrials.gov

Largest completed trials with posted results that list Mepolizumab 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 (1 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
Asthma12,76754.5
53.6–55.4ROR 73.2 · calibrated p 1e-6 ✓
48.3 EB05 47.6 · IC025 +5.6
3/3 methods agree
Likely indication confounding
term in indications; also in warnings
age-adj. PRR 64.0 · serious PRR 56.6NCT04718389: 2/855 (0.2%) on Mepolizumab (serious AE)
Dyspnoea (shortness of breath)10,5768.1
7.9–8.2ROR 10.0 · calibrated p 0.032 ✓
7.9 EB05 7.8 · IC025 +3.0
3/3 methods agree
Labeled adverse reaction
exact term
age-adj. PRR 9.2 · serious PRR 9.0NCT04718389: 1/855 (0.1%) on Mepolizumab (serious AE)
Wheezing7,13158.1
56.8–59.5ROR 67.8 · calibrated p 2e-6 ✓
51.2 EB05 50.2 · IC025 +5.6
3/3 methods agree
Not in label — unassessedage-adj. PRR 76.2 · serious PRR 61.2not reported in cached trials
Product dose omission issue6,63610.1
9.9–10.3ROR 11.5 · calibrated p 0.019 ✓
9.9 EB05 9.7 · IC025 +3.3
3/3 methods agree
Reporting / coding artifactage-adj. PRR 12.3 · serious PRR 9.1 · 74% consumernot reported in cached trials
Cough5,1007.9
7.7–8.1ROR 8.7 · calibrated p 0.052
7.7 EB05 7.6 · IC025 +2.9
3/3 methods agree
Labeled adverse reaction
exact term
age-adj. PRR 10.3 · serious PRR 10.9NCT04718389: 42/855 (4.9%) on Mepolizumab
Therapeutic product effect incomplete5,05132.6
31.7–33.5ROR 36.2 · calibrated p 9e-5 ✓
30.3 EB05 29.6 · IC025 +4.9
3/3 methods agree
Reporting / coding artifactage-adj. PRR 52.7 · serious PRR 51.4not reported in cached trials
Drug ineffective (drug did not work)4,6221.5
1.5–1.5ROR 1.5 · calibrated p 0.669
1.5 EB05 1.5 · IC025 +0.5Reporting / coding artifactage-adj. PRR 2.3 · serious PRR 2.8not reported in cached trials
Loss of personal independence in daily activities4,24141.5
40.3–42.8ROR 45.3 · calibrated p 2e-5 ✓
37.8 EB05 36.9 · IC025 +5.2
3/3 methods agree
Not in label — unassessedage-adj. PRR 51.4 · serious PRR 45.2not reported in cached trials
Sleep disorder due to a general medical condition3,118101.5
97.7–105.4ROR 108.2 · calibrated p 6e-8 ✓
81.8 EB05 79.4 · IC025 +6.3
3/3 methods agree
Not in label — unassessedage-adj. PRR 118.9 · serious PRR 147.4not reported in cached trials
Fatigue (tiredness)3,0781.7
1.6–1.7ROR 1.7 · calibrated p 0.788
1.7 EB05 1.6 · IC025 +0.7Labeled adverse reaction
exact term
age-adj. PRR 2.0 · serious PRR 2.2NCT04718389: 23/855 (2.7%) on Mepolizumab
Off label use (used outside approved label)3,0731.5
1.5–1.6ROR 1.5 · calibrated p 0.667
1.5 EB05 1.5 · IC025 +0.5Reporting / coding artifactage-adj. PRR 1.4 · serious PRR 1.3not reported in cached trials
Malaise (feeling unwell)2,7762.7
2.6–2.8ROR 2.8 · calibrated p 0.698
2.7 EB05 2.6 · IC025 +1.4
3/3 methods agree
Not in label — unassessedage-adj. PRR 3.5 · serious PRR 3.6not reported in cached trials
Condition aggravated2,7433.9
3.7–4.0ROR 4.1 · calibrated p 0.368
3.9 EB05 3.7 · IC025 +1.9
3/3 methods agree
Reporting / coding artifactage-adj. PRR 4.8 · serious PRR 4.6not reported in cached trials
Headache2,6961.8
1.8–1.9ROR 1.9 · calibrated p 0.876
1.8 EB05 1.8 · IC025 +0.8Labeled adverse reaction
exact term
age-adj. PRR 2.3 · serious PRR 2.6NCT04718389: 1/855 (0.1%) on Mepolizumab (serious AE)

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 Mepolizumab?

In FDA FAERS, the most frequently co-reported reaction terms for Mepolizumab are asthma, dyspnoea, wheezing, cough, pneumonia, loss of personal independence in daily activities. 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 Mepolizumab have an FDA boxed warning?

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

Do FAERS signals prove that Mepolizumab 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.