Abatacept 87.5mg/0.7ml solution for injection pre-filled syringes
Requires a prescription from a doctor or prescriber
Shortage warning
Current supply issues
High shortage warning
Healthcare professionals should be aware of the potential for delayed onset of angioedema and the distinction between bradykinin- and histamine-mediated cases, as treatment strategies differ significantly and bradykinin-medi…
Affected areas: UK
Official documents, adverse reaction reporting, and safety monitoring
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Official medicine documents
Safety monitoring data
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 Abatacept
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Submit a Yellow Card report to the MHRA
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 Abatacept
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EudraVigilance data is published by the European Medicines Agency (EMA). A suspected adverse reaction is not necessarily caused by the medicine.
1 branded products available
Part of the Orencia brand family (generic: Abatacept)
MHRA licensed products
View all licensed products for Abatacept on the MHRA register
WHO defined daily dose (DDD)
27 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(14)
Abatacept, adalimumab, etanercept and tocilizumab for treating juvenile idiopathic arthritis (TA373)
Adalimumab, etanercept, infliximab, rituximab and abatacept for the treatment of rheumatoid arthritis after the failure of a TNF inhibitor (TA195)
Adalimumab, etanercept, infliximab and abatacept for treating moderate rheumatoid arthritis after conventional DMARDs have failed (TA715)
Abatacept for treating psoriatic arthritis after DMARDs (terminated appraisal) (TA568)
Adalimumab, etanercept, infliximab, certolizumab pegol, golimumab, tocilizumab and abatacept for rheumatoid arthritis not previously treated with DMARDs or after conventional DMARDs only have failed (TA375)
Sarilumab for moderate to severe rheumatoid arthritis (TA485)
Upadacitinib for treating severe rheumatoid arthritis (TA665)
Baricitinib for moderate to severe rheumatoid arthritis (TA466)
Golimumab for the treatment of rheumatoid arthritis after the failure of previous disease-modifying anti-rheumatic drugs (TA225)
Certolizumab pegol for treating rheumatoid arthritis after inadequate response to a TNF-alpha inhibitor (TA415)
Tofacitinib for moderate to severe rheumatoid arthritis (TA480)
Filgotinib for treating moderate to severe rheumatoid arthritis (TA676)
Rheumatoid arthritis in adults: management (NG100)
Tocilizumab for the treatment of rheumatoid arthritis (TA247)
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
Pharmacy stock checkers
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: 14 · Randomised trials: 25 · 2005–2026
Showing the 50 most relevant studies, sorted by most relevant.
Carol A. Langford, D. Cuthbertson, Steven R. Ytterberg, et al.
Arthritis & rheumatology (Hoboken, N.J.), 2017
D. Khanna, C. Spino, S. Johnson, et al.
Arthritis & rheumatology (Hoboken, N.J.), 2019
Andrew Cope, M. Jasenecova, Joana C Vasconcelos, et al.
Lancet, 2024
C. Langford, D. Cuthbertson, S. Ytterberg, et al.
Arthritis & Rheumatology, 2017
Juergen Rech, K. Tascilar, M. Hagen, et al.
Lancet, 2024
A. Tjärnlund, Q. Tang, C. Wick, et al.
Annals of the Rheumatic Diseases, 2017
W. Russell, B. Bundy, Mark S. Anderson, et al.
Diabetes Care, 2023
A. Pugliesi, Amanda Borges de Oliveira, Ana Oliveira, et al.
Advances in Rheumatology, 2023
Jane A. O’Halloran, E. Ko, K. Anstrom, et al.
JAMA, 2023
Hannah A. Blair, E. Deeks
Drugs, 2017
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
14.3 days
Mechanism
Abatacept is a selective costimulation modulator - like CTLA-4, the drug has sho…
Food interactions
None known
Human targets
2 targets
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
10 mg/k
Half-life
14.3 days
13.1 (8-25) days in RA subjects;
14.3 days when subcutaneously administered to adult RA patients.
Volume of distribution
0.07 L/kg
* 0.09 L/kg [Healthy Subjects, IV administration]
* 0.11…
Elimination
Clearance
0.23 mL
* 0.22…
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
[L48811]
In patients two years of age and older, abatacept is also indicated for the treatment of moderately-to-severely active juvenile idiopathic arthritis.
[L20504]
Abatacept is also indicated for the prophylaxis of acute graft-versus-host disease, in combination with [methotrexate] and a calcineurin inhibitor such as [tacrolimus], in patients two years of age and older who are undergoing hematopoietic stem cell transplantation from a matched or 1 allele-mismatched unrelated donor.
[L20504]
Known interactions with other medications. Always consult a healthcare professional.
Showing 50 of 1041 interactions
How the body processes this drug — absorption, distribution, metabolism, and elimination
13.1 (8-25) days in RA subjects;
14.3 days when subcutaneously administered to adult RA patients.
* 0.09 L/kg [Healthy Subjects, IV administration]
* 0.11 L/kg [RA patients, subcutaneous administration]
* 0.22 mL/h/kg [RA Patients after multiple 10 mg/kg Intravenous Infusions]
* 0.4 mL/h/kg [juvenile idiopathic arthritis patients].
The mean systemic clearance is 0.28 mL/h/kg when a subcutaneously administered to adult RA patients.
The clearance of abatacept increases with increasing body weight.
Proteins and enzymes this drug interacts with in the body
PMID:38467718
Acts as the primary auxiliary signal augmenting the MHC/TCR signal in naive T-cells together with the CD28 receptor which is constitutively expressed on the cell surface of T-cells .
PMID:12196291
In turn, activates different signaling pathways such as NF-kappa-B or MAPK leading to the production of different cytokines .
PMID:10438913
In addition, CD28/CD80 costimulatory signal stimulates glucose metabolism and ATP synthesis of T-cells by activating the PI3K/Akt signaling pathway .
PMID:12121659
Also acts as a regulator of PDL1/PDCD1 interactions to limit excess engagement of PDL1 and its inhibitory role in immune responses .
PMID:36727298
Expressed on B-cells, plays a critical role in regulating interactions between B-cells and T-cells in both early and late germinal center responses, which are crucial for the generation of effective humoral immune responses (By similarity)
PMID:12196291
May play a critical role in the early events of T-cell activation and costimulation of naive T-cells, such as deciding between immunity and anergy that is made by T-cells within 24 hours after activation .
PMID:7527824
Also involved in the regulation of B cells function, plays a role in regulating the level of IgG(1) produced. Upon CD40 engagement, activates NF-kappa-B signaling pathway via phospholipase C and protein kinase C activation (By similarity)
ATC L04AA24
Chemical identifiers
CAS, UNII, InChI Key and database cross-references
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Chemical identifiers
CAS, UNII, InChI Key and database cross-references
Linked compound data from DrugBank Open Data (CC BY-NC 4.0)
Abatacept
Additional database identifiers
Drugs Product Database (DPD)
15233
HUGO Gene Nomenclature Committee (HGNC)
HGNC:1700
GenAtlas
CD80
GeneCards
CD80
GenBank Gene Database
M27533
GenBank Protein Database
306916
Guide to Pharmacology
2744
UniProt Accession
CD80_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:1705
GenAtlas
CD86
GeneCards
CD86
GenBank Gene Database
L25259
GenBank Protein Database
439839
Guide to Pharmacology
2745
UniProt Accession
CD86_HUMAN
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
ATC classifications (Wikidata)
Linked open data from Wikidata (Q2697833), a free and open knowledge base operated by the Wikimedia Foundation. Data is available under the Creative Commons CC0 1.0 Public Domain Dedication.