Mepolizumab side effects: what 49,291 FDA adverse event reports show
Drug class
Interleukin-5 Antagonist
Brand names
Nucala
Who reports
49,291 reports · 63% serious · 3,989 with death outcome · 68% female
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).
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.
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). 1,162 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 |
|---|---|---|---|---|---|---|
| Plethysmography | 25 | 10,447.2 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 — unassessed | serious n=25 · ♀ 100% (drug 68%) · 100% consumer | not reported in cached trials |
| Total lung capacity increased | 186 | 925.3 715.3–1,197.1ROR 928.8 · calibrated p 2e-16 ✓ | 280.3 EB05 248.0 · IC025 +7.1 3/3 methods agree | Not in label — unassessed | serious n=185 · ♀ 94% (drug 68%) | not reported in cached trials |
| Sputum culture | 25 | 870.6 437.4–1,732.7ROR 871.0 · calibrated p 9e-14 ✓ | 232.8 EB05 165.8 · IC025 +4.8 3/3 methods agree | Lab value / disease marker | serious n=25 | not reported in cached trials |
| Heart sounds | 63 | 797.8 523.6–1,215.5ROR 798.8 · calibrated p 5e-15 ✓ | 253.8 EB05 205.4 · IC025 +6.0 3/3 methods agree | Not in label — unassessed | serious n=63 · ♀ 100% (drug 68%) | not reported in cached trials |
| Airway remodelling | 68 | 516.7 362.1–737.1ROR 517.4 · calibrated p 2e-13 ✓ | 217.5 EB05 177.4 · IC025 +6.0 3/3 methods agree | Not in label — unassessed | serious n=68 · ♀ 33% (drug 68%) | not reported in cached trials |
| Hepatic enzyme | 73 | 469.3 336.0–655.5ROR 470.0 · calibrated p 5e-13 ✓ | 209.5 EB05 172.2 · IC025 +6.1 3/3 methods agree | Not in label — unassessed | serious n=73 · ♀ 100% (drug 68%) · 100% clinician | not reported in cached trials |
| Asthma-chronic obstructive pulmonary disease overlap syndrome | 255 | 411.4 346.2–489.0ROR 413.6 · calibrated p 6e-13 ✓ | 204.6 EB05 184.4 · IC025 +7.0 3/3 methods agree | Labeled (related wording) related wording | serious n=254 | not reported in cached trials |
| Reversible airways obstruction | 226 | 334.9 281.2–398.9ROR 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=226 | not reported in cached trials |
| Vital capacity decreased | 184 | 294.6 244.0–355.7ROR 295.7 · calibrated p 2e-11 ✓ | 170.2 EB05 150.5 · IC025 +6.6 3/3 methods agree | Not in label — unassessed | serious n=184 | not reported in cached trials |
| Total lung capacity abnormal | 146 | 265.3 215.6–326.3ROR 266.1 · calibrated p 5e-11 ✓ | 159.3 EB05 138.8 · IC025 +6.4 3/3 methods agree | Not in label — unassessed | serious n=145 · ♀ 0% (drug 68%) | not reported in cached trials |
| Prolonged expiration | 100 | 259.6 202.3–333.1ROR 260.1 · calibrated p 7e-11 ✓ | 155.8 EB05 131.8 · IC025 +6.2 3/3 methods agree | Not in label — unassessed | serious n=100 | not reported in cached trials |
| Hypocholesterolaemia | 109 | 233.6 184.8–295.2ROR 234.1 · calibrated p 2e-10 ✓ | 146.4 EB05 124.7 · IC025 +6.2 3/3 methods agree | Not in label — unassessed | serious n=109 · ♀ 100% (drug 68%) · 100% clinician | not reported in cached trials |
| Pulmonary vasculitis | 177 | 214.4 178.9–256.9ROR 215.2 · calibrated p 3e-10 ✓ | 139.9 EB05 123.5 · IC025 +6.4 3/3 methods agree | Not in label — unassessed | serious n=177 · ♀ 0% (drug 68%) | not reported in cached trials |
| Eosinophilic granulomatosis with polyangiitis | 671 | 212.1 193.4–232.7ROR 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 abnormal | 227 | 186.4 159.4–217.9ROR 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=217 | not reported in cached trials |
| Central nervous system mass | 27 | 173.6 110.8–271.9ROR 173.7 · calibrated p 7e-9 ✓ | 113.3 EB05 81.8 · IC025 +4.6 3/3 methods agree | Not in label — unassessed | serious n=27 · ♀ 0% (drug 68%) · 100% clinician | not reported in cached trials |
| Bronchopulmonary aspergillosis allergic | 262 | 170.3 147.5–196.5ROR 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=262 | not reported in cached trials |
| Spirometry abnormal | 163 | 163.3 136.3–195.7ROR 163.9 · calibrated p 3e-9 ✓ | 116.1 EB05 101.9 · IC025 +6.2 3/3 methods agree | Lab value / disease marker | serious n=162 · ♀ 10% (drug 68%) | not reported in cached trials |
| Eosinophilic bronchitis | 56 | 162.5 119.4–221.3ROR 162.7 · calibrated p 5e-9 ✓ | 112.9 EB05 90.2 · IC025 +5.4 3/3 methods agree | Labeled (related wording) related wording | serious n=56 · ♀ 26% (drug 68%) | not reported in cached trials |
| Capillaritis | 67 | 141.4 107.2–186.5ROR 141.6 · calibrated p 1e-8 ✓ | 102.9 EB05 83.8 · IC025 +5.5 3/3 methods agree | Not in label — unassessed | serious n=67 · ♀ 0% (drug 68%) | not reported in cached trials |
| Wall motion score index abnormal | 27 | 137.6 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 marker | serious n=27 · ♀ 0% (drug 68%) · 100% clinician | not reported in cached trials |
| Antacid therapy | 29 | 134.7 88.6–204.6ROR 134.7 · calibrated p 4e-8 ✓ | 95.8 EB05 70.0 · IC025 +4.6 3/3 methods agree | Reporting / coding artifact | serious n=29 · ♀ 0% (drug 68%) · 100% clinician | not reported in cached trials |
| Lung diffusion disorder | 38 | 134.6 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 — unassessed | serious n=38 · ♀ 42% (drug 68%) | not reported in cached trials |
| Mite allergy | 153 | 134.0 111.7–160.8ROR 134.5 · calibrated p 1e-8 ✓ | 100.5 EB05 87.8 · IC025 +6.0 3/3 methods agree | Not in label — unassessed | serious n=153 · ♀ 14% (drug 68%) | not reported in cached trials |
| Fungal disease carrier | 24 | 132.0 83.4–208.8ROR 132.0 · calibrated p 6e-8 ✓ | 93.3 EB05 66.0 · IC025 +4.4 3/3 methods agree | Reporting / coding artifact | serious n=24 | not reported in cached trials |
| Acquired factor v deficiency | 26 | 129.3 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 — unassessed | serious n=26 · ♀ 0% (drug 68%) | not reported in cached trials |
| Coagulation factor v level abnormal | 29 | 128.9 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 marker | serious n=29 · ♀ 0% (drug 68%) | not reported in cached trials |
| Facet joint syndrome | 723 | 126.5 116.4–137.4ROR 128.3 · calibrated p 2e-8 ✓ | 97.1 EB05 91.3 · IC025 +6.4 3/3 methods agree | Not in label — unassessed | serious n=723 · ♀ 100% (drug 68%) · 93% clinician | not reported in cached trials |
| Respiratory gas exchange disorder | 79 | 115.0 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 — unassessed | serious n=79 | not reported in cached trials |
| Nasal polypectomy | 31 | 108.0 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 — unassessed | serious n=27 · 100% consumer | not reported in cached trials |
| Obstructive airways disorder | 2,175 | 102.8 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 78.2 | NCT02105948: 1/184 (0.5%) on Mepolizumab; 1/229 (0.4%) control (serious AE) |
| Vocal cord dysfunction | 97 | 102.4 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 — unassessed | serious n=96 · ♀ 93% (drug 68%) | not reported in cached trials |
| Sleep disorder due to a general medical condition | 3,118 | 101.5 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 — unassessed | age-adj. PRR 118.9 · serious PRR 147.4 | not reported in cached trials |
| Bronchial wall thickening | 136 | 98.0 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=136 | not reported in cached trials |
| Pulmonary function test abnormal | 290 | 96.8 85.2–109.9ROR 97.4 · calibrated p 2e-7 ✓ | 78.4 EB05 71.1 · IC025 +5.9 3/3 methods agree | Reporting / coding artifact | serious n=289 | not reported in cached trials |
| Malignant melanoma stage 0 | 33 | 94.5 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 — unassessed | serious n=33 · ♀ 0% (drug 68%) · 100% clinician | not reported in cached trials |
| Congenital hiatus hernia | 40 | 93.4 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 — unassessed | serious n=40 · ♀ 0% (drug 68%) · 100% clinician | not reported in cached trials |
| Coagulation factor deficiency | 29 | 92.5 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 — unassessed | serious n=29 · ♀ 0% (drug 68%) | not reported in cached trials |
| Laryngeal stenosis | 102 | 91.1 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 — unassessed | serious n=102 · ♀ 100% (drug 68%) · 72% consumer | not reported in cached trials |
| Nasal polyps | 849 | 90.7 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=770 | not 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.
| Concept | Reports | PRR 95% CI | Reading |
|---|---|---|---|
| Interstitial lung disease | 763 | 3.43.2–3.6 | signal |
| Serious infection | 5,900 | 3.33.2–3.3 | signal |
| Opportunistic infection | 609 | 1.91.8–2.1 | raised |
| Liver injury | 1,343 | 1.91.8–2.0 | raised |
| Depression | 1,250 | 1.91.8–2.0 | raised |
| Hyperglycaemia / diabetes | 1,511 | 1.91.8–2.0 | raised |
| Fall / fracture | 1,509 | 1.71.6–1.8 | raised |
| Anaphylaxis / angioedema | 349 | 1.21.1–1.3 | raised |
| Venous thromboembolism | 595 | 1.21.1–1.3 | raised |
| Arrhythmia / qt | 522 | 1.11.1–1.2 | raised |
| Heart failure | 396 | 0.90.9–1.0 | no difference |
| Malignancy | 806 | 0.90.8–1.0 | lower than other drugs |
| Pancreatitis | 168 | 0.90.8–1.0 | no difference |
| Tendon disorder | 73 | 0.80.6–1.0 | no difference |
| Myocardial infarction | 383 | 0.80.7–0.9 | lower than other drugs |
| Stroke | 377 | 0.60.6–0.7 | lower 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).
- NCT04718389 — A Study of GSK3511294 (Depemokimab) Compared With Mepolizumab or Benralizumab in Participants With Severe Asth (N=1717, PHASE3; 154 AE terms posted; arms: Depemokimab 100mg SC; Mepolizumab 100 mg / Benralizumab 30 mg )
- NCT02105948 — Study to Evaluate Efficacy and Safety of Mepolizumab for Frequently Exacerbating Chronic Obstructive Pulmonary (N=837, PHASE3; 202 AE terms posted; arms: Placebo - High Stratum; Mepolizumab 100 mg - High Stratum; Placebo - Low Stratum; Mepolizumab 100 mg - Low Stratum)
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.
| Reaction | Reports | PRR 95% CI · ROR · χ²/p | EBGM EB05 · IC025 | Label screen | Serious-only & strata | Trial cross-check |
|---|---|---|---|---|---|---|
| Asthma | 12,767 | 54.5 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 56.6 | NCT04718389: 2/855 (0.2%) on Mepolizumab (serious AE) |
| Dyspnoea (shortness of breath) | 10,576 | 8.1 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 9.0 | NCT04718389: 1/855 (0.1%) on Mepolizumab (serious AE) |
| Wheezing | 7,131 | 58.1 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 — unassessed | age-adj. PRR 76.2 · serious PRR 61.2 | not reported in cached trials |
| Product dose omission issue | 6,636 | 10.1 9.9–10.3ROR 11.5 · calibrated p 0.019 ✓ | 9.9 EB05 9.7 · IC025 +3.3 3/3 methods agree | Reporting / coding artifact | age-adj. PRR 12.3 · serious PRR 9.1 · 74% consumer | not reported in cached trials |
| Cough | 5,100 | 7.9 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 10.9 | NCT04718389: 42/855 (4.9%) on Mepolizumab |
| Therapeutic product effect incomplete | 5,051 | 32.6 31.7–33.5ROR 36.2 · calibrated p 9e-5 ✓ | 30.3 EB05 29.6 · IC025 +4.9 3/3 methods agree | Reporting / coding artifact | age-adj. PRR 52.7 · serious PRR 51.4 | not reported in cached trials |
| Pneumonia (lung infection) | 4,644 | 6.2 6.0–6.3ROR 6.7 · calibrated p 0.111 | 6.1 EB05 5.9 · IC025 +2.6 3/3 methods agree | Labeled (related wording) related wording | age-adj. PRR 6.0 · serious PRR 5.8 | NCT04718389: 1/855 (0.1%) on Mepolizumab (serious AE) |
| Drug ineffective (drug did not work) | 4,622 | 1.5 1.5–1.5ROR 1.5 · calibrated p 0.669 | 1.5 EB05 1.5 · IC025 +0.5 | Reporting / coding artifact | age-adj. PRR 2.3 · serious PRR 2.8 | not reported in cached trials |
| Loss of personal independence in daily activities | 4,241 | 41.5 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 — unassessed | age-adj. PRR 51.4 · serious PRR 45.2 | not reported in cached trials |
| Sleep disorder due to a general medical condition | 3,118 | 101.5 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 — unassessed | age-adj. PRR 118.9 · serious PRR 147.4 | not reported in cached trials |
| Fatigue (tiredness) | 3,078 | 1.7 1.6–1.7ROR 1.7 · calibrated p 0.788 | 1.7 EB05 1.6 · IC025 +0.7 | Labeled adverse reaction exact term | age-adj. PRR 2.0 · serious PRR 2.2 | NCT04718389: 23/855 (2.7%) on Mepolizumab |
| Off label use (used outside approved label) | 3,073 | 1.5 1.5–1.6ROR 1.5 · calibrated p 0.667 | 1.5 EB05 1.5 · IC025 +0.5 | Reporting / coding artifact | age-adj. PRR 1.4 · serious PRR 1.3 | not reported in cached trials |
| Malaise (feeling unwell) | 2,776 | 2.7 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 — unassessed | age-adj. PRR 3.5 · serious PRR 3.6 | not reported in cached trials |
| Condition aggravated | 2,743 | 3.9 3.7–4.0ROR 4.1 · calibrated p 0.368 | 3.9 EB05 3.7 · IC025 +1.9 3/3 methods agree | Reporting / coding artifact | age-adj. PRR 4.8 · serious PRR 4.6 | not reported in cached trials |
| Headache | 2,696 | 1.8 1.8–1.9ROR 1.9 · calibrated p 0.876 | 1.8 EB05 1.8 · IC025 +0.8 | Labeled adverse reaction exact term | age-adj. PRR 2.3 · serious PRR 2.6 | NCT04718389: 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.
- Plethysmography — n=25, PRR 10,447.2
- Total lung capacity increased — n=186, PRR 925.3
- Heart sounds — n=63, PRR 797.8
- Airway remodelling — n=68, PRR 516.7
- Hepatic enzyme — n=73, PRR 469.3
- Vital capacity decreased — n=184, PRR 294.6
- Total lung capacity abnormal — n=146, PRR 265.3
- Prolonged expiration — n=100, PRR 259.6
- Hypocholesterolaemia — n=109, PRR 233.6
- Pulmonary vasculitis — n=177, PRR 214.4
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
- FDA label via openFDA (set ID fefb887c-e4ac-431e-8893-e9d1a5a63fea, effective 20250806; matched on
openfda.generic_name.exact:"MEPOLIZUMAB") - 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, 1,202 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
MEPOLIZUMAB, 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.