Atracurium besilate 25mg/2.5ml solution for injection ampoules
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Atracurium besilate 25mg/2.5ml solution for injection ampoules
Atracurium besilate 25mg/2.5ml solution for injection ampoules
Atracurium besilate 25mg/2.5ml solution for injection ampoules
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: 7 · Randomised trials: 10 · 1981–2026
Showing the 50 most relevant studies, sorted by most relevant.
Alipour M, Ghanei S, Sheikh S, et al.
2025
- Dexmedetomidine
- Atracurium
- Intubation, Intratracheal
Karimi M, Ghaheri A, Saleh K, et al.
2024
- Atracurium
- Electrocardiography
- Anesthesia, General
BackgroundMuscle relaxants are used during surgery, but their impact on ECG may differ, potentially affecting cardiac safety. This study aimed to compare the effects of Atracurium versus Cisatracurium on QT interval changes in patients undergoing cataract surgery.MethodThis double-blind, parallel-group randomized clinical trial (RCT) was conducted in 2023 in Hamadan, Iran. A total of 80 patients undergoing cataract surgery under general anesthesia were randomly assigned to receive either Atracurium (n = 40) or Cisatracurium (n = 40). QT interval changes were measured at four time points to assess and compare the corrected QT interval (QTc) between the two groups. Data were analyzed using SPSS version 29, and a p-value ResultsCisatracurium demonstrated significant reductions in QTc from pre-anesthesia to post-anesthesia and through recovery, with values of -9.325 ms (P = 0.045), -9.925 ms (P = 0.038), and - 19.359 ms (P = 0.016), respectively. Atracurium also showed reductions but a notable increase in QTc after anesthesia to the end of surgery (32.322 ms, P = 0.0019). Throughout the procedure, Cisatracurium maintained shorter QTc intervals compared to Atracurium (e.g., T0: 420.07 ms vs. 434.75 ms, P = 0.03), but post-recovery, no significant differences were observed (Cisatracurium: 440.05 ms; Atracurium: 439.80 ms, P = 0.489).ConclusionsAtracurium causes more QT prolongation than Cisatracurium. While both affect QTc intervals, Cisatracurium has a more stable impact on cardiac repolarization, making it safer for patients at risk of QT prolongation. Cisatracurium's minimal impact on cardiovascular function, especially in patients with low ejection fraction, makes it the preferred choice for maintaining cardiac stability.Trial registrationIRCT20120215009014N441.
Abstract licence: CC BY
Okonkwo TC, Adigun TA, Idowu OK
2026
- Atracurium
- Pancuronium
- Neuromuscular Nondepolarizing Agents
BackgroundSuxamethonium, a rapid-acting muscle relaxant, has been conventionally preferred during rapid sequence induction (RSI). The priming principle, which uses non-depolarising muscle relaxants, is an alternative in situations where it is contraindicated. Unfortunately, its efficacy has not been sufficiently documented in Nigerian patients.AimsThe study aimed to use atracurium and pacuronium to evaluate the efficacy of the priming principle.Materials and methodsIn this randomised controlled trial, ninety adults undergoing elective surgery under general anaesthesia were randomly allocated into three equal groups. Group A (Atracurium), Group P (Pancuronium) and Group C (control) received 0.05 mg/kg atracurium, 0.01 mg/kg pancuronium and 1 ml saline, respectively, as the priming agent. Three minutes after, anaesthesia was induced with 2 mg/kg propofol and then the intubating dose of pancuronium administered. The onset time of neuromuscular block, intubating condition and occurrence of muscle weakness during the priming interval were noted. Data were analysed using the Statistical Package for the Social Sciences version 25, and a P ResultsThe mean onset time in Groups A, P and C was 215.7 ± 59.9 s, 237.1 ± 76.5 s and 265.8 ± 72.0 s, respectively, P = 0.024. Post hoc analysis showed that the onset time was only significant between Groups A and C (P = 0.02). The intubating condition was comparable in all groups (P = 0.25). The incidence of muscle weakness during the priming interval was 6.67% in the priming groups.ConclusionIn adults, priming with atracurium but not pancuronium shortens the onset time of pancuronium. However, during RSI, where a fast onset is crucial, the shortened onset time with priming is not clinically relevant.
Abstract licence: CC BY-NC-SA
Shilpa Bansal, Mridul M Pandit Rao, Minnu Mridul Pandit Rao
Journal of Clinical and Diagnostic Research, 2023
Luo R, Ge Y, Chen Y, et al.
2025
- Postoperative Complications
- Neostigmine
- Laparoscopy
BackgroundIt is uncertain whether neostigmine reversal improves postoperative pulmonary outcomes. This study aimed to evaluate the association between neostigmine and postoperative atelectasis, and other complications in elderly patients undergoing laparoscopic pancreaticoduodenectomy (LPD).MethodsThis single-center retrospective cohort study included elderly patients who underwent LPD between 2019 and 2022, using cis-atracurium as the sole neuromuscular blocking agent. Participants were divided into two groups based on exposure to neostigmine: the neostigmine reversal group (exposed) and the control group (not exposed). The primary endpoint was the incidence of atelectasis within the first 3 postoperative days. Secondary endpoints included the incidence of pneumonia, pleural effusion, acute respiratory distress syndrome (ARDS), time to extubation, length of stay in the post-anesthesia care unit (PACU) and hospital, reintubation, postoperative blood gas analysis, 30-day readmission, and 30-day mortality. Propensity score matching (PSM) was performed based on baseline and intraoperative characteristics to minimize potential bias.ResultsOf the 501 patients initially included, 302 were successfully matched after PSM at a 1:5 ratio, comprising 89 patients in the neostigmine reversal group and 213 in the control group. Compared to the control group, the incidence of postoperative atelectasis was lower in the neostigmine reversal group (OR 0.43 [95% CI 0.24-0.75], p = 0.003) in elderly patients undergoing elective LPD. For secondary outcomes, time to extubation (Median [IQR] 20.00 [10.00-32.50] min vs. 25.00 [15.00-41.00] min, p ConclusionsIn this single-center PSM study, neostigmine reversal was associated with lower incidence of atelectasis within the first 3 postoperative days, shorter time to extubation, shorter length of stay in the PACU, and increased OI at 2 h after extubation in elderly patients undergoing elective LPD. Postoperative atelectasis was associated with older age, greater intraoperative total fluid infusion, and the absence of neostigmine reversal. These results should be interpreted as hypothesis-generating, and warrant validation through randomized controlled trials.
Abstract licence: CC BY-NC-ND
X. Durrmeyer, S. Breinig, O. Claris, et al.
JAMA, 2018
Ronald D. Miller, Stephen M. Rupp, Dennis M. Fisher, et al.
Anesthesiology, 1984
- Acid-Base Equilibrium
- Age Factors
- Anesthesia
H. Berg, J. Viby-Mogensen, J. Roed, et al.
Acta Anaesthesiologica Scandinavica, 1997
- Postoperative Complications
- Hypoxia
- Atracurium
K. Leslie, D. Sessler, A. Bjorksten, et al.
Anesthesia & Analgesia, 1995
- Hypothermia, Induced
- Anesthesia
- Atracurium
E. Sundman, H. Witt, R. Olsson, et al.
Anesthesiology, 2000
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
Not available
Mechanism
Not available
Food interactions
None known
Human targets
None mapped
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Known interactions with other medications. Always consult a healthcare professional.
Showing 50 of 1119 interactions
ATC M03AC04
Chemical identifiers
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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)
Atracurium
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Linked open data from Wikidata (Q165660), 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.