Lixisenatide 10micrograms/0.2ml solution for injection 3ml pre-filled disposable devices
Lixisenatide is a glucagon-like peptide-1 (GLP-1) receptor agonist used in the treatment of type II diabetes mellitus (T2DM).
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 Lixisenatide
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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 Lixisenatide
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Learn about EU pharmacovigilance and safety monitoring
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
WHO defined daily dose (DDD)
20 microgram
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 NHS dm+d BNF mapping files. Contains public sector information licensed under the Open Government Licence v3.0.
Therapeutically similar medicines
Similarity based on WHO Anatomical Therapeutic Chemical (ATC) classification and NHS BNF section grouping. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
NHS prescribing volume and spending trends
Clinical guidelines and formulary information
British National Formulary
Lixisenatide
Source: British National Formulary, NICE. Joint Formulary Committee. Contains public sector information licensed under the Open Government Licence v3.0.
NICE clinical guidance(1)
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
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Supply & product information
Official product databases and supply status monitoring
Pharmacy links redirect to the retailer's own search and do not represent real-time stock levels. emc (electronic medicines compendium) is operated by Datapharm Ltd. Shortage information sourced from NHS Specialist Pharmacy Service (SPS), sps.nhs.uk.
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 codes from NHS Business Services Authority (NHSBSA). 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.
Pharmacology and chemical data from DrugBank
Key facts
Drug status
Approved
Major interactions
None known
Half-life
3 hours
Mechanism
The activation of the GLP-1 receptor by lixisenatide results in the activation of adenylyl cyclase.
Food interactions
2 warnings
Human targets
1 target
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
1-3.5 hours
Half-life
3 hours
[L48400]…
Protein binding
55%
[L764]
Volume of distribution
100 L
[L48400]
Metabolism
[L48400]
Elimination
[L48400]
Clearance
35 L/h
[L48400]
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
[L48400]
It is also available in combination with [insulin glargine] for the same indication.
[L48405]
Known interactions with other medications. Always consult a healthcare professional.
Showing 50 of 1217 interactions
[L48400]
Overdose is associated with GI side effects typical of GLP-1 receptor agonists.
How the body processes this drug — absorption, distribution, metabolism, and elimination
[L48400]
[L48400]
[L764]
[L48400]
[L48400]
[L48400]
[L48400]
Proteins and enzymes this drug interacts with in the body
PMID:19861722 PMID:26308095 PMID:27196125 PMID:28514449 PMID:7517895 PMID:8216285 PMID:8405712
Ligand binding triggers activation of a signaling cascade that leads to the activation of adenylyl cyclase and increased intracellular cAMP levels .
PMID:19861722 PMID:26308095 PMID:27196125 PMID:28514449 PMID:7517895 PMID:8216285 PMID:8405712
Plays a role in regulating insulin secretion in response to GLP-1 (By similarity)
ATC A10AE54
ATC A10BJ03
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)
Lixisenatide
Additional database identifiers
Drugs Product Database (DPD)
22870
ChemSpider
17295846
HUGO Gene Nomenclature Committee (HGNC)
HGNC:4324
GenAtlas
GLP1R
GeneCards
GLP1R
GenBank Gene Database
U01104
GenBank Protein Database
405082
Guide to Pharmacology
249
UniProt Accession
GLP1R_HUMAN
Patent information
21 active patents, 18 expired
Source: DrugBank · CC BY-NC 4.0. Patent data sourced from national patent offices. Expiry dates may not reflect extensions, regulatory exclusivity periods, or legal challenges.
DrugBank citations
If you use DrugBank data in your research, please cite the following publications: