Clevidipine 25mg/50ml emulsion for infusion vials
Clevidipine is a dihydropyridine L-type calcium channel blocker that is selective for vascular smooth muscle and is indicated for blood pressure reduction when oral therapy is not an option.
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Suspected adverse reactions reported for Clevidipine
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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.
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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: 17 · Randomised trials: 2 · 2004–2026
Showing the 50 most relevant studies, sorted by most relevant.
Ali Seifi, Amirhossein Azari Jafari, Seyyedmohammadsadeq Mirmoeeni, et al.
Clinical Neurology and Neurosurgery, 2023
- Cerebrovascular Disorders
- Hypertension
- Antihypertensive Agents
Ángel Espinosa, Javier Ripollés‐Melchor, R. Casans‐Francés, et al.
PLoS ONE, 2016
- Antihypertensive Agents
- Atrial Fibrillation
- Blood Pressure
Alice Bottussi, Jacopo D’Andria Ursoleo, Viviana Teresa Agosta, et al.
Frontiers in Medicine, 2025
Khan NN, Zurayyir EJ, Alghamdi AM, et al.
2024
A hypertensive crisis is defined as a sudden and significant rise in blood pressure. The blood pressure reading is 180/120 mmHg or higher. A hypertensive crisis is a medical emergency. It can lead to a heart attack, stroke, or other life-threatening medical problems. Investigating the management of the hypertensive crisis was the goal of this study. English-language articles were collected from 2010 to 2024 demonstrating the management of the hypertensive crisis. Overall, there were 15 articles. Surveys and analyses of national databases were the most widely used methods (n=15). The scientific studies documented (1) all investigative studies or reports that included a hypertensive crisis diagnosis, (2) data integrity and reproducibility, and (3) management studies. Other studies show that acute severe hypertension in the hospital is associated with high rates of mortality and morbidity, particularly with new or worsening end-organ damage. The problem is linked to poor medical adherence, but alarmingly low follow-up rates are likely to contribute to a high recurrence rate. The treatment of acute severe hypertension varies according to the hospital unit (medical ward or intensive care unit), medication, and blood pressure targets or thresholds. Because of a lack of evidence-based guidance, arbitrary blood pressure control targets are used, or blood pressure targets are crudely extrapolated from guidelines intended primarily for outpatient management. Patients with acute aortic dissection need to be administered intravenous esmolol within 5 to 10 minutes in order to lower their blood pressure right away. The goal is to maintain a systolic reading of less than 120 mm Hg. Vasodilators such as nitroglycerin or nitroprusside may be administered if the blood pressure persists following beta blocking. Intravenous administration of clevidipine, nicardipine, or phentolamine is required; the initial dose is 5 mg, with subsequent doses given every 10 minutes as necessary to achieve the desired reduction in blood pressure.
Abstract licence: CC BY
Monika Widiastuti, Dewi Yulianti Bisri, Iwan Abdul Rachman
Scientific Reports, 2024
- Hypertension
- Pyridines
- Antihypertensive Agents
Seifi A, Jafari AA, Mirmoeeni S, et al.
2022
Abstract Background: The term "cerebrovascular diseases (CVDs)" refers to a broad category of diseases that affect the brain's blood vessels and cerebral circulation. According to a substantial body of evidence, controlling acute hypertension (HTN) by antihypertensive drugs such as clevidipine and nicardipine can be a highly efficient method of lowering the incidence of CVDs. The aim of this systematic review and meta-analysis is to compare and analyze the outcomes of clevidipine and nicardipine in CVD patients for the first time. Methods: For identifying potential eligible studies, two independent researchers systematically searched PubMed, Scopus, and Web of Science online databases, and the gray literature search, including Google scholar and hand-searching, were performed. Included studies were any observational (Retrospective/prospective cohort and cross-sectional) literature that compares adult patients receiving clevidipine or nicardipine for controlling HTN in the setting of CVD. Results: We reviewed 487 articles and finally included 5 studies, including 546 patients (211 received clevidipine, and 335 received nicardipine). The pooled standardized mean difference (SMD) for time to goal SBP was -0.04 (95% CI: [-0.66; 0.58], p-value: 0.86, I2: 79.0%, pooled MD: -12.90 min), meaning that the clevidipine group has shorter time to goal systolic blood pressure (SBP) compared to nicardipine. The pooled SMD for total volume infusion was -0.52 (95% CI: [-0.93; -0.12], p-value: 0.03, I2: 0.0%, pooled MD: -1118.81 mL), showing a notable less total volume infused to patients in the clevidipine group. Conclusion: We found that clevidipine reaches the SBP goal faster than nicardipine; however, there is no statistically significant difference between the two drugs. The total volume infused to achieve the goal SBP is significantly less in the clevidipine group. Both clevidipine and nicardipine are safe, and their adverse effects are comparable. Further prospective studies in a blinded and protocolized condition are needed to compare clevidipine and nicardipine in CVD patients on a large scale.
Abstract licence: CC BY 4.0
Neil Singla, David C. Warltier, Sweeta D. Gandhi, et al.
Anesthesia & Analgesia, 2008
- Acute Disease
- Calcium Channel Blockers
- Cardiac Surgical Procedures
Lv Q, Chen C, Lin L, et al.
2026
- Hypertension
- Pyridines
- Nicardipine
Solomon Aronson, Cornelius Dyke, Kevin A. Stierer, et al.
Anesthesia & Analgesia, 2008
- Cardiac Surgical Procedures
- Acute Disease
- Antihypertensive Agents
Alexandru Ulici, J. Jancik, Timothy Lam, et al.
The American Journal of Emergency Medicine, 2017
- Acute Disease
- Aortic Dissection
- Blood Pressure
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
53 found
Half-life
1 minute
Mechanism
Possibly by deforming the channel, inhibiting ion-control gating mechanisms, and…
Food interactions
None known
Human targets
4 targets
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Half-life
1 minute
Protein binding
99.5%
Metabolism
Elimination
63-74%
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
Known interactions with other medications. Always consult a healthcare professional.
Showing 50 of 1766 interactions
How the body processes this drug — absorption, distribution, metabolism, and elimination
Proteins and enzymes this drug interacts with in the body
They are blocked by dihydropyridines (DHP), phenylalkylamines, and by benzothiazepines. Activates at more negative voltages and does not undergo calcium-dependent inactivation (CDI), due to incoming calcium ions, during depolarization
They are blocked by dihydropyridines (DHP), phenylalkylamines, and by benzothiazepines
PMID:12181424 PMID:15454078 PMID:15863612 PMID:16299511 PMID:17224476 PMID:20953164 PMID:23677916 PMID:24728418 PMID:26253506 PMID:27218670 PMID:29078335 PMID:29742403 PMID:30023270 PMID:30172029 PMID:34163037 PMID:8099908
Mediates influx of calcium ions into the cytoplasm, and thereby triggers calcium release from the sarcoplasm (By similarity). Plays an important role in excitation-contraction coupling in the heart. Required for normal heart development and normal regulation of heart rhythm .
PMID:15454078 PMID:15863612 PMID:17224476 PMID:24728418 PMID:26253506
Required for normal contraction of smooth muscle cells in blood vessels and in the intestine.
Essential for normal blood pressure regulation via its role in the contraction of arterial smooth muscle cells .
PMID:28119464
Long-lasting (L-type) calcium channels belong to the 'high-voltage activated' (HVA) group (Probable)
Enzymes involved in drug metabolism — important for understanding drug interactions
ATC C08CA16
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)
Clevidipine
Additional database identifiers
Drugs Product Database (DPD)
20686
ChemSpider
135722
BindingDB
50088387
HUGO Gene Nomenclature Committee (HGNC)
HGNC:1393
GenAtlas
CACNA1F
GeneCards
CACNA1F
GenBank Gene Database
AJ006216
GenBank Protein Database
3183953
Guide to Pharmacology
531
UniProt Accession
CAC1F_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:1397
GenAtlas
CACNA1S
GeneCards
CACNA1S
GenBank Gene Database
U30707
GenBank Protein Database
1698403
Guide to Pharmacology
528
UniProt Accession
CAC1S_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:1391
GenAtlas
CACNA1D
GeneCards
CACNA1D
GenBank Gene Database
M76558
GenBank Protein Database
179764
Guide to Pharmacology
530
UniProt Accession
CAC1D_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:1390
GenAtlas
CACNA1C
GeneCards
CACNA1C
GenBank Gene Database
M92270
Guide to Pharmacology
529
UniProt Accession
CAC1C_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:2623
GenAtlas
CYP2C9
GeneCards
CYP2C9
GenBank Gene Database
AY341248
Guide to Pharmacology
1326
UniProt Accession
CP2C9_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:2625
GenAtlas
CYP2D6
GeneCards
CYP2D6
GenBank Gene Database
M20403
GenBank Protein Database
181350
Guide to Pharmacology
1329
UniProt Accession
CP2D6_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:2631
GeneCards
CYP2E1
GenBank Gene Database
J02625
GenBank Protein Database
181360
Guide to Pharmacology
1330
UniProt Accession
CP2E1_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:2621
GeneCards
CYP2C19
GenBank Gene Database
M61854
GenBank Protein Database
181344
Guide to Pharmacology
1328
UniProt Accession
CP2CJ_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:2637
GenAtlas
CYP3A4
GeneCards
CYP3A4
GenBank Gene Database
M18907
Guide to Pharmacology
1337
UniProt Accession
CP3A4_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:983
GenAtlas
BCHE
GeneCards
BCHE
GenBank Gene Database
M32391
GenBank Protein Database
1311630
Guide to Pharmacology
2471
UniProt Accession
CHLE_HUMAN
DrugBank citations
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Structured knowledge from the free knowledge base
ATC classifications (Wikidata)
Linked open data from Wikidata (Q5132338), 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.