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Yellow Card reports
The MHRA Yellow Card scheme collects reports of suspected side effects from healthcare professionals and patients. View the Drug Analysis Profile (iDAP) for real-world adverse reaction data.
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Suspected adverse reactions reported for Mepolizumab
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Data from the MHRA Yellow Card scheme. A reported reaction does not necessarily mean the medicine caused it. Contains public sector information licensed under the Open Government Licence v3.0.
EudraVigilance
The European Medicines Agency (EMA) collects suspected adverse reaction reports from across the EU/EEA through the EudraVigilance system. Search for safety data on this medicine.
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Suspected adverse reactions reported for Mepolizumab
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1 branded products available
WHO defined daily dose (DDD)
3.6 mg
Not a recommended dose. The DDD is the assumed average maintenance dose per day for a drug used for its main indication in adults. It is a statistical measure used for research and comparison purposes only.
Source: WHO Collaborating Centre for Drug Statistics Methodology, distributed via the NHS dm+d supplementary BNF/ATC mapping files (NHSBSA). Contains public sector information licensed under the Open Government Licence v3.0.
Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
NHS prescribing volume and spending trends
Guidelines from the National Institute for Health and Care Excellence
NICE clinical guidance(11)
Mepolizumab for treating severe eosinophilic asthma (TA671)
Mepolizumab for maintenance treatment of uncontrolled chronic obstructive pulmonary disease with raised blood eosinophils (TA1166)
Mepolizumab for treating severe hypereosinophilic syndrome (terminated appraisal) (TA846)
Mepolizumab for treating eosinophilic granulomatosis with polyangiitis (terminated appraisal) (TA845)
Mepolizumab for treating severe chronic rhinosinusitis with nasal polyps (terminated appraisal) (TA847)
Benralizumab for treating severe eosinophilic asthma (TA565)
Dupilumab for treating severe asthma with type 2 inflammation (TA751)
Benralizumab for treating relapsing or refractory eosinophilic granulomatosis with polyangiitis (TA1096)
Reslizumab for treating severe eosinophilic asthma (TA479)
Asthma pathway (BTS, NICE, SIGN) (NG244)
Tezepelumab for treating severe asthma (TA880)
Source: National Institute for Health and Care Excellence (NICE). Contains public sector information licensed under the Open Government Licence v3.0.
Check stock at pharmacies and supply information
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Search for this medicine at major UK pharmacy chains. These links open the retailer's own website — results depend on their current online catalogue.
Supply & safety information
Official UK regulator monitoring and safety alerts
Pharmacy links redirect to the retailer's own search and do not represent real-time stock levels. Shortage and safety information sourced from MHRA drug safety updates (gov.uk, Crown Copyright under OGL v3.0).
Codes for healthcare professionals and prescribing systems
These codes are used by healthcare IT systems and prescribers to identify this medicine.
NHS UK identifiers
Browse tools
SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. BNF code shown is the factual mapping value distributed by NHS Business Services Authority (NHSBSA) in the dm+d supplementary file under OGL v3.0; it is not affiliated with, nor licensed from, the publishers of the British National Formulary. ATC codes from the WHO Collaborating Centre for Drug Statistics Methodology (whocc.no).
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
Reviews & meta-analyses: 21 · Randomised trials: 18 · 2012–2026
Showing the 50 most relevant studies, sorted by most relevant.
I. Agache, Jessica Beltran, C. Akdis, et al.
Allergy, 2020
Joseph K. Han, C. Bachert, W. Fokkens, et al.
The Lancet. Respiratory medicine, 2021
G. Chupp, E. Bradford, F. Albers, et al.
The Lancet. Respiratory medicine, 2017
F. Roufosse, J. Kahn, M. Rothenberg, et al.
The Journal of allergy and clinical immunology, 2020
D. Charles, Jemma Shanley, Sasha Temple, et al.
Clinical and Experimental Allergy, 2022
Qingwu Wu, Yana Zhang, W. Kong, et al.
International Archives of Allergy and Immunology, 2021
I. Dighriri, Anas I Alnughaythir, Amna A Albesisi, et al.
Cureus, 2023
Rishma Gattu, Michelle Demory Beckler, Marc M. Kesselman
Cureus, 2024
Sinclair De Frías J, Velo A, Olivero L, et al.
2026
- Pulmonary Disease, Chronic Obstructive
- Pulmonary Eosinophilia
- Antibodies, Monoclonal, Humanized
IntroductionUp to 40% of patients with COPD have an eosinophilic phenotype, which increases the risk of acute exacerbations. Mepolizumab, an anti - IL-5 monoclonal antibody, has shown mixed results. We conducted a systematic review and meta-analysis to evaluate the efficacy and safety of mepolizumab 100 mg in eosinophilic COPD.MethodsFollowing PRISMA and Cochrane guidelines, we searched PubMed, Embase, and Cochrane Central through 18 May 2025. Randomized controlled trials comparing mepolizumab 100 mg versus placebo in eosinophilic COPD were included. The primary outcome was the annualized rate of moderate or severe exacerbations. Data were pooled using random-effects models.ResultsFour RCTs (1,953 patients) were included. Mepolizumab reduced annualized rate of moderate or severe exacerbations (Rate Ratio 0.80; 95% CI: 0.73-0.89; p p p = 0.004). Patient-reported outcomes did not improve. Safety was favorable, with reduced serious adverse events, including deaths (RR 0.84; 95% CI: 0.73-0.98; p = 0.03).ConclusionsMepolizumab reduces exacerbations with good safety in eosinophilic COPD, though without improvement in quality-of-life outcomes.
Abstract licence: CC BY
T. Nopsopon, Grace Lassiter, Ming-Li Chen, et al.
The Journal of allergy and clinical immunology, 2022
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Pharmacology and chemical data from DrugBank
Key facts
Drug status
Approved
Major interactions
None known
Half-life
22 days
Mechanism
Hypereosinophilia is typically considered as an absolute eosinophil count of 150…
Food interactions
None known
Human targets
1 target
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
80%
Half-life
22 days
[L16518]
Volume of distribution
3.6 L
[L16518]
Metabolism
[L16518]
Clearance
0.28 L
[L16518]
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
Mepolizumab is a fully-humanized recombinant IgG1 kappa monoclonal antibody directed against IL-5 produced in Chinese hamster ovary cells. Mepolizumab was first approved by the FDA on November 4, 2015, as an add-on therapy for severe asthma and marketed under the brand name Nucala by GlaxoSmithKline. This indication was subsequently expanded to cover EGPA on December 12, 2017, and HES on September 25, 2020.[L16518]
[L16518]
Mepolizumab is additionally indicated as an add-on maintenance treatment of chronic rhinosinusitis with nasal polyps (CRSwNP) in patients ≥18 years old with inadequate response to nasal corticosteroids.
[L16518]
Known interactions with other medications. Always consult a healthcare professional.
Showing 50 of 681 interactions
[L16518]
Typically, eosinophils arise from both CD34+ and dual CD34+, IL-5 receptor-positive (IL-5R+) progenitor cells, which is in part mediated by the cytokines IL-5, IL-3, and granulocyte-macrophage colony-stimulating factor (GM-CSF).[A221063] Although there exists a population of eosinophils that are insensitive to IL-5 levels, the main population of inflammatory eosinophils proliferates and migrates into the tissue in response to IL-5.[A221063] Mepolizumab is a fully-humanized monoclonal IgG1 kappa antibody that binds IL-5 with a dissociation constant of 100 pM, preventing IL-5 from binding to and subsequently activating IL-5R+ cells.[L16518] This reduction lowers circulating blood eosinophil levels and therefore exerts a beneficial effect in eosinophilic disease; the exact mechanistic nature of mepolizumab action has not been definitively determined.[A221048][A221053][A221058][A221063][A221068][L16518] Not all patients will benefit from mepolizumab treatment, such as those with milder asthma or those with a sub-type of HES that is independent of IL-5 signalling.[A221048][A221063]
How the body processes this drug — absorption, distribution, metabolism, and elimination
[L16518]
[L16518]
[L16518]
[L16518]
[L16518]
Proteins and enzymes this drug interacts with in the body
PMID:2653458 PMID:9010276
Also acts on activated and resting B-cells to induce immunoglobulin production, growth, and differentiation (By similarity). Mechanistically, exerts its biological effects through a receptor composed of IL5RA subunit and the cytokine receptor common subunit beta/CSF2RB .
PMID:1495999 PMID:22528658
Binding to the receptor leads to activation of various kinases including LYN, SYK and JAK2 and thereby propagates signals through the RAS-MAPK and JAK-STAT5 pathways respectively PMID:7613138
ATC R03DX09
Chemical identifiers
CAS, UNII, InChI Key and database cross-references
Show
Chemical identifiers
CAS, UNII, InChI Key and database cross-references
Linked compound data from DrugBank Open Data (CC BY-NC 4.0)
Mepolizumab
Additional database identifiers
DrugBank citations
If you use DrugBank data in your research, please cite the following publications:
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Structured knowledge from the free knowledge base
Linked open data from Wikidata (Q3306175), a free and open knowledge base operated by the Wikimedia Foundation. Data is available under the Creative Commons CC0 1.0 Public Domain Dedication. WHO INN from the World Health Organization.