Terlipressin 1mg powder and solvent for solution for injection vials
Requires a prescription from a doctor or prescriber
Terlipressin is a synthetic analogue of vasopressin, which is an endogenous neurohormone that acts as a vasoconstrictor.[A2601] It is a prodrug of [lypressin], or lysine vasopressin.
Official documents, adverse reaction reporting, and safety monitoring
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Drug safety updates
MHRA alerts for Terlipressin
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 Terlipressin
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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 Terlipressin
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3 branded products available
MHRA licensed products
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Glypressin 1mg powder and solvent for solution for injection vials
Terlipressin 1mg powder and solvent for solution for injection vials
Variquel 1mg powder and solvent for solution for injection vials
WHO defined daily dose (DDD)
12 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 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(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
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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. 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: 30 · Randomised trials: 18 · 1990–2026
Showing the 50 most relevant studies, sorted by most relevant.
George N. Ioannou, Jenny Doust, Don C. Rockey
Cochrane Database of Systematic Reviews, 2003
- Terlipressin
- Acute Disease
- Catheterization
Vinod Arora, Rakhi Maiwall, Vijayaraghavan Rajan, et al.
Hepatology, 2018
- Terlipressin
- Norepinephrine
- Vasoconstrictor Agents
George N. Ioannou, Jenny Doust, Don C. Rockey
Alimentary Pharmacology & Therapeutics, 2002
- Terlipressin
- Esophageal and Gastric Varices
- Gastrointestinal Hemorrhage
Arun J. Sanyal, Thomas Boyer, Guadalupe García–Tsao, et al.
Gastroenterology, 2008
- Terlipressin
- Germany
- Hepatorenal Syndrome
M. Cavallin, Patrick S. Kamath, Manuela Merli, et al.
Hepatology, 2015
- Terlipressin
- Albumins
- Analysis of Variance
Prashant Solanki, Atul Chawla, Ramesh Garg, et al.
Journal of Gastroenterology and Hepatology, 2003
- Terlipressin
- Blood Pressure
- Creatinine
Àngels Escorsell, L Ruíz del Arbol, Ramón Planas, et al.
Hepatology, 2000
- Terlipressin
- Acute Disease
- Hemorrhage
Ary Serpa Neto, Antônio Paulo Nassar, Sérgio Oliveira Cardoso, et al.
Critical Care, 2012
- Terlipressin
- Hemodynamics
- Lypressin
Antônio Paulo Nassar, Alberto Queiróz Farias, Luiz Augusto Carneiro D′Albuquerque, et al.
PLoS ONE, 2014
- Terlipressin
- Hepatorenal Syndrome
- Lypressin
Lise Lotte Gluud, Kurt Christensen, Erik Christensen, et al.
Cochrane Database of Systematic Reviews, 2012
- Terlipressin
- Albumins
- Hepatorenal Syndrome
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
1 found
Half-life
0.9 hours
Mechanism
Endogenous vasopressin, also referred to as antidiuretic hormone (ADH) or argini…
Food interactions
None known
Human targets
3 targets
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
1 mg
Half-life
0.9 hours
[L43217]
Volume of distribution
6.3 L
[L43217]
Metabolism
Elimination
1%
[L43217]
Clearance
27.4 L/h
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
[L43217]
Known interactions with other medicines. Always consult a healthcare professional.
Showing 50 of 396 interactions
[L43217]
Vasopressin is considered a stress hormone as it is released into the bloodstream in response to various volume and pressure stimuli, such as pain, surgery, syncope and shock.[A2601][A2605][A252677] Shock conditions such as hypovolemia initially cause an increase in the release of vasopressin to maintain organ perfusion; however, as the shock state progresses, plasma vasopressin concentrations decrease due to several causes such as depleted stores of vasopressin in refractory shock and a central inhibitory effect of initially elevated vasopressin levels on further vasopressin release.[A2605]
Terlipressin is a synthetic vasopressin analogue that can cause sustained increases in blood pressure in patients with shock conditions.[A2605] It exhibits twice the selectivity for vasopressin V1 receptors versus V2 receptors. Terlipressin is pharmacologically active but acts as a prodrug for [lypressin] (also known as lysine vasopressin), a vasoconstrictor and antidiuretic agent. The exact mechanism of action of terlipressin is not fully understood; however, terlipressin works to cause vasoconstriction in shock and other conditions associated with vasodilation. Hepatorenal syndrome (HRS) is caused by splanchnic and systemic arterial vasodilation along with a reduced mean arterial pressure (MAP) and cardiac output, resulting in a marked decrease in effective circulating volume.[A252672] Terlipressin is thought to increase renal blood flow in patients with HRS-1 by reducing portal hypertension and blood circulation in portal vessels and increasing effective arterial volume and mean arterial pressure (MAP).[L43217]
Terlipressin increases arterial pressure (diastolic, systolic, and mean) and decreases heart rate in patients with hepatorenal syndrome type 1 (HRS-1). After the administration of a single 0.85 mg dose of terlipressin in patients with HRS-1, cardiovascular effects were observed within five minutes after dosing and were maintained for at least six hours after dosing. The maximum change in blood pressure and heart rate occurred at 1.2 to two hours post-dose.[L43217]
How the body processes this drug — absorption, distribution, metabolism, and elimination
Plasma concentrations of terlipressin demonstrate proportional increases with the dose administered.
[L43217]
[L43217]
[L43217]
Due to the ubiquitous nature of peptidases in body tissues, it is unlikely that the metabolism of terlipressin will be affected by disease state or other drugs.
[L43217]
[L43217]
[L43217]
Proteins and enzymes this drug interacts with in the body
ATC H01BA04
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)
Terlipressin
Additional database identifiers
ChemSpider
65067
HUGO Gene Nomenclature Committee (HGNC)
HGNC:895
GenAtlas
AVPR1A
GeneCards
AVPR1A
GenBank Gene Database
L25615
GenBank Protein Database
667068
Guide to Pharmacology
366
UniProt Accession
V1AR_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:896
GenAtlas
AVPR1B
GeneCards
AVPR1B
GenBank Gene Database
D31833
GenBank Protein Database
563982
Guide to Pharmacology
367
UniProt Accession
V1BR_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:897
GenAtlas
AVPR2
GeneCards
AVPR2
GenBank Gene Database
U04357
GenBank Protein Database
28418
Guide to Pharmacology
368
UniProt Accession
V2R_HUMAN
DrugBank citations
If you use DrugBank data in your research, please cite:
- DrugBank 6.02024Recommended citationKnox C., Wilson M., Klinger C.M., et alDrugBank 6.0: the DrugBank Knowledgebase for 2024Nucleic Acids Res. 2024 Jan 552(D1):D1265-D1275
- DrugBank 5.02018Wishart D.S., Feunang Y.D., Guo A.C., et alDrugBank 5.0: a major update to the DrugBank database for 2018Nucleic Acids Res. 2017 Nov 846(D1):D1074-D1082
- DrugBank 4.02014Law V., Knox C., Djoumbou Y., et alDrugBank 4.0: shedding new light on drug metabolismNucleic Acids Res. 2014 Jan 142(1):D1091-7
- DrugBank 3.02011Knox C., Law V., Jewison T., et alDrugBank 3.0: a comprehensive resource for 'omics' research on drugsNucleic Acids Res. 2011 Jan39(Database issue):D1035-41
- DrugBank 2.02008Wishart D.S., Knox C., Guo A.C., et alDrugBank: a knowledgebase for drugs, drug actions and drug targets.Nucleic Acids Research2008 Jan36(Database issue):D901-6
- DrugBank 1.02006Wishart D.S., Knox C., Guo A.C., et alDrugBank: a comprehensive resource for in silico drug discovery and exploration.Nucleic Acids Research2006 Jan 134(Database issue):D668-72