Cisatracurium besilate 150mg/30ml solution for injection vials
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Cisatracurium besilate 150mg/30ml solution for injection vials
Cisatracurium besilate 150mg/30ml solution for injection vials
Cisatracurium besilate 150mg/30ml solution for injection vials
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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Codes for healthcare professionals and prescribing systems
These codes are used by healthcare IT systems and prescribers to identify this medicine.
NHS UK identifiers
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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. 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: 7 · Randomised trials: 18 · 1999–2026
Showing the 50 most relevant studies, sorted by most relevant.
Vascular and Endovascular Review, 2025
Mengya Cao, Hui-qiong Huang, Jianbin Tong, et al.
BMC Anesthesiology, 2023
Behzad Nazemroaya, Sahand Taei
Archives of Anesthesia and Critical Care, 2024
Swati Taneja, Amardeep Kaur, Shalvi Mahajan, et al.
Archives of Anesthesia and Critical Care, 2023
F. Rokhtabnak, Saeed Safari, Soudabeh Djalali Motlagh, et al.
Iranian Journal of Medical Sciences, 2023
Sapna Suresh, A. Hrishi, Jithendra Thiruvathra, et al.
Surgical Neurology International, 2025
Background: Transcranial motor-evoked potentials (TcMEPs) are essential for monitoring spinal cord integrity during spine surgery, but are highly sensitive to neuromuscular blocking agents. This study compared the effects of rocuronium reversed with sugammadex versus cisatracurium on TcMEP amplitude and recovery characteristics during thoracic and lumbar spine surgery. Methods: A double-blinded, randomized controlled trial was conducted in 60 patients undergoing elective spine surgery. Participants were randomized to receive either rocuronium 0.6 mg/kg with sugammadex reversal (Group R, n = 30) or cisatracurium 0.15 mg/kg (Group C, n = 30). Primary outcomes included MEP amplitude and latency at 5, 10, 20, 30, and 60 min post-obtaining the fourth twitch in the train-of-four (TOF) sequence with a peripheral nerve stimulator. Secondary outcomes measured TOF recovery times and intraoperative adverse events. Data were presented as mean ± standard deviation. The normally distributed continuous variables were compared using Student’s t-test, with P < 0.05 considered statistically significant. Results: Group R demonstrated significantly higher MEP amplitudes and shorter MEP latency at all time points from baseline till 30 min as compared to group C (P < 0.05). TOF recovery was significantly faster in group R (P < 0.001) as compared to group C. Group R had a higher incidence of nociception-induced movements (P = 0.076) and excessive field movements (P = 0.118), which was not statistically significant. The total propofol dosage in group R was significantly higher (P = 0.042) compared to group C. No postoperative neurological deficits occurred in either group. Conclusion: At similar TOF ratios, sugammadex-facilitated reversal of rocuronium results in superior quality of MEP parameters, such as higher MEP amplitude and shorter MEP latency, with no significant difference in adverse movements compared to single-dose cisatracurium.
Abstract licence: CC BY-NC-SA
Rui An, Chunnan Lin, Zeguang Lu, et al.
BMC Anesthesiology, 2025
- Ketamine
- Propofol
- Atracurium
Gegal Pruthi, K. Bharathi, P. Simha, et al.
The Indian Anaesthetists Forum, 2025
Karimi M, Ghaheri A, Saleh K, et al.
2024
- Atracurium
- Electrocardiography
- Anesthesia, General
Feng Y, Jia JM, Cheng YX, et al.
2025
- Propofol
- Benzodiazepines
- Flumazenil
BackgroundLaparoscopic partial hepatectomy, characterized by significant surgical trauma, profound stress responses, prolonged duration, and high anesthetic requirements, may lead to delayed recovery or emergence agitation. Whether remimazolam and propofol combined with flumazenil reversal can accelerate the recovery and enhance hemodynamic stability remains controversial.MethodsFifty patients aged 18-70 years with American Society of Anesthesiologists (ASA) class I-III and Child-Pugh classification A or B undergoing elective laparoscopic partial hepatectomy were enrolled. Participants were randomly assigned to either the remimazolam combined with propofol group (RP group) or the propofol group (P group). Both groups received intravenous sufentanil and cisatracurium for induction, followed by either remimazolam-propofol with flumazenil reversal or propofol alone. Emergence parameters, including time to obey verbal commands, BIS over 80, and tracheal tube removal were recorded. The Sedation-Agitation Scale (SAS) and Visual Analog Scale (VAS) scores at predefined intervals, hemodynamics, and adverse events were recorded.ResultsThe time to obey verbal commands (p), BIS over 80 (p =0.0011), and tracheal tube removal (p=0.0002) were all significantly shorter in the RP group than in the P group. The SAS score after 30 min (p=0.0488) in the PACU was significantly higher, but the VAS score after 15 min (p=0.0086) and 30 min (p=0.0084) in the PACU, were significantly lower in the RP group than in the P group. MAP at T1 (p=0.0470) was significantly lower in the P group than in the RP group. In addition, the RP group demonstrated reduced post-induction hypotension, required no postoperative rescue analgesia, and reported no emergence agitation.ConclusionCompared to propofol alone, remimazolam-propofol with flumazenil reversal provides faster and more complete recovery, superior hemodynamic stability perioperatively, and reduced analgesic requirements in laparoscopic partial hepatectomy patients.
Abstract licence: CC BY-NC
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
22 minutes
Mechanism
Like other non-depolarising neuromuscular blocking agents, cisatracurium binds c…
Food interactions
None known
Human targets
4 targets
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
6%
[A253602][L43577]
…
Half-life
22 minutes
[L43577]
Protein binding
[L43577]
Volume of distribution
145 mL
[L43577]
…
Metabolism
Elimination
80%
Clearance
4.57 mL/min/kg
[L43577]
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
[L43577]
Known interactions with other medicines. Always consult a healthcare professional.
Showing 50 of 1379 interactions
If complete neuromuscular blockade is evident or suspected, cholinesterase inhibitors should not be administered. The reversal of paralysis may not be sufficient to maintain a patent airway and an appropriate level of spontaneous ventilation.
[L43577]
The long-term carcinogenicity of cisatracurium has not been evaluated. In an in vitro mouse lymphoma forward gene mutation assay, cisatracurium besylate led to mutations in the presence and absence of exogenous metabolic activation.
Other assays did not show evidence of mutagenicity or clastogenicity.
[L43577]
The use of cisatracurium may lead to residual paralysis, as well as a higher risk of seizure. Medication errors increase the risk of death, and the use of certain drugs may potentiate the neuromuscular blocking action of cisatracurium.[L43577]
How the body processes this drug — absorption, distribution, metabolism, and elimination
[A253602][L43577]
Cisatracurium is metabolized into laudanosine and monoquaternary alcohol metabolite (MQA). Following the IV infusion of cisatracurium, the Cmax of laudanosine and MQA were 6% and 11% of the parent compound, respectively.
[L43577]
Compared to young patients, the volume of distribution of cisatracurium is slightly larger in elderly patients, which also leads to longer half-life values. The plasma clearance of cisatracurium was not affected by age.
Patients with hepatic impairment have a slightly higher volume of distribution and plasma clearance values; however, these minor pharmacokinetic differences are not considered clinically significant. Additionally, the pharmacokinetic parameters of cisatracurium in patients with end-stage renal disease were similar to those detected in healthy adult patients.
[L43577]
[L43577]
[L43577]
[L43577]
The volume of distribution of cisatracurium besylate is small due to its relatively large molecular weight and high polarity.
[A253602]
The MQA can also undergo Hofmann elimination, but the rate of this process is slower than the one detected for cisatracurium. Laudanosine is further metabolized to desmethyl metabolites that are conjugated with glucuronic acid and excreted in the urine. Laudanosine may cause transient hypotension and, in higher doses, cerebral excitatory effects when administered to several animal species; however, the effects of laudanosine in humans have not been established.
[L43577]
[L43577]
In healthy male patients (n=6) given 14C-cisatracurium, 4% of the recovered dose was found in feces, and 95% was found in urine, mostly as conjugated metabolites. Less than 10% of the cisatracurium dose was excreted as the unchanged patent drug.
In another group of patients with Foley catheters for surgical management given non-radiolabeled cisatracurium (n=12), 15% of the cisatracurium dose was excreted unchanged in urine.
[L43577]
[L43577]
Proteins and enzymes this drug interacts with in the body
PMID:20881005 PMID:31488329 PMID:8663494 PMID:8906617 PMID:9203638
CHRNB4 forms heteropentameric neuronal acetylcholine receptors with CHRNA2, CHRNA3 and CHRNA4, as well as CHRNA5 and CHRNB3 as accesory subunits .
PMID:11118490 PMID:20881005 PMID:8663494
CHRNA3:CHRNB4 being predominant in neurons of the autonomic ganglia, it is known as ganglionic nicotinic receptor .
PMID:31488329
CHRNA3:CHRNB4 or CHRNA3:CHRNA5:CHRNB4 play also an important role in the habenulo-interpeduncular tract, modulating the mesolimbic dopamine system and affecting reward circuits and addiction (By similarity). Hypothalamic CHRNA3:CHRNB4 nAChR activation by nicotine leads to activation of POMC neurons and a decrease in food intake (By similarity)
PMID:18723036
CHRNA2 forms heteropentameric neuronal acetylcholine receptors with CHRNB2 and CHRNB4 and plays a role in nicotine dependence PMID:24467848 PMID:27493220
ATC M03AC11
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)
Cisatracurium
Additional database identifiers
Drugs Product Database (DPD)
11084
ChemSpider
56615
ZINC
ZINC000238809664
HUGO Gene Nomenclature Committee (HGNC)
HGNC:13800
GenAtlas
CHRNA10
GeneCards
CHRNA10
GenBank Gene Database
AJ278118
GenBank Protein Database
12053839
Guide to Pharmacology
470
UniProt Accession
ACH10_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:1956
GenAtlas
CHRNA2
GeneCards
CHRNA2
GenBank Gene Database
U62431
GenBank Protein Database
1458110
Guide to Pharmacology
463
UniProt Accession
ACHA2_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:1957
GeneCards
CHRNA3
GenBank Gene Database
M86383
GenBank Protein Database
177898
Guide to Pharmacology
464
UniProt Accession
ACHA3_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:1958
GenAtlas
CHRNA4
GeneCards
CHRNA4
GenBank Gene Database
L35901
GenBank Protein Database
755648
Guide to Pharmacology
465
UniProt Accession
ACHA4_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:1959
GeneCards
CHRNA5
GenBank Gene Database
M83712
GenBank Protein Database
177926
UniProt Accession
ACHA5_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:15963
GeneCards
CHRNA6
GenBank Gene Database
U62435
GenBank Protein Database
1458118
Guide to Pharmacology
467
UniProt Accession
ACHA6_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:1960
GenAtlas
CHRNA7
GeneCards
CHRNA7
GenBank Gene Database
X70297
GenBank Protein Database
496607
Guide to Pharmacology
468
UniProt Accession
ACHA7_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:14079
GenAtlas
CHRNA9
GeneCards
CHRNA9
GenBank Gene Database
AJ243342
GenBank Protein Database
6688136
Guide to Pharmacology
469
UniProt Accession
ACHA9_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:1962
GenAtlas
CHRNB2
GeneCards
CHRNB2
GenBank Gene Database
X53179
GenBank Protein Database
32017
UniProt Accession
ACHB2_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:1963
GeneCards
CHRNB3
GenBank Gene Database
U62438
GenBank Protein Database
1458124
UniProt Accession
ACHB3_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:1964
GeneCards
CHRNB4
GenBank Gene Database
U62439
GenBank Protein Database
1458126
UniProt Accession
ACHB4_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:1956
GenAtlas
CHRNA2
GeneCards
CHRNA2
GenBank Gene Database
U62431
GenBank Protein Database
1458110
Guide to Pharmacology
463
UniProt Accession
ACHA2_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:1955
GeneCards
CHRNA1
Guide to Pharmacology
462
UniProt Accession
ACHA_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:1951
GenAtlas
CHRM2
GeneCards
CHRM2
GenBank Gene Database
M16404
GenBank Protein Database
177990
Guide to Pharmacology
14
UniProt Accession
ACM2_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