Sugammadex 200mg/2ml solution for injection vials
Requires a prescription from a doctor or prescriber
Sugammadex is a selective relaxant binding agent indicated for reversal of neuromuscular blockade induced by rocuronium bromide and vecuronium bromide during surgery.
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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 Sugammadex
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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.
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Suspected adverse reactions reported for Sugammadex
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EudraVigilance data is published by the European Medicines Agency (EMA). A suspected adverse reaction is not necessarily caused by the medicine.
13 branded products available
MHRA licensed products
View all licensed products for Sugammadex on the MHRA register
Bridion 200mg/2ml solution for injection vials
Sugammadex 200mg/2ml solution for injection vials
Sugammadex 200mg/2ml solution for injection vials
Sugammadex 200mg/2ml solution for injection vials
Sugammadex 200mg/2ml solution for injection vials
Sugammadex 200mg/2ml solution for injection vials
Sugammadex 200mg/2ml solution for injection vials
Sugammadex 200mg/2ml solution for injection vials
Sugammadex 200mg/2ml solution for injection vials
Sugammadex 200mg/2ml solution for injection vials
Sugammadex 200mg/2ml solution for injection vials
Sugammadex 200mg/2ml 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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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: 28 · Randomised trials: 21 · 2017–2026
Showing the 50 most relevant studies, sorted by most relevant.
A. Hristovska, P. Duch, Mikkel Allingstrup, et al.
Anaesthesia, 2018
A. Hristovska, P. Duch, Mikkel Allingstrup, et al.
The Cochrane database of systematic reviews, 2017
Hong-Mei Liu, Hong Yu, Yiding Zuo, et al.
BMC Anesthesiology, 2023
B. Togioka, D. Yanez, M. Aziz, et al.
British journal of anaesthesia, 2020
Nancy Abou Nafeh, M. Aouad, Amro Khalili, et al.
Anesthesia & Analgesia, 2024
Leslie K, Braat S, Darvall JN, et al.
2026
Ni Z, Sun R, Zhang Q, et al.
2025
- Urinary Retention
- Postoperative Complications
- Sugammadex
BackgroundPostoperative urinary retention (POUR) is a frequent complication following general anesthesia. There is growing interest in whether sugammadex, a neuromuscular blockade (NMB) reversal agent that does not require anticholinergic coadministration, might reduce its incidence. This systematic review and meta-analysis aimed to evaluate the effects of sugammadex on POUR and other postoperative recovery outcomes, such as 30-day readmission rates and postoperative pain scores (POPS).MethodsPubMed, Cochrane, Embase, and Web of Science were comprehensively searched for studies published through June 3, 2024. Randomized controlled trials (RCTs) and cohort studies comparing sugammadex with conventional reversal agents or no reversal agents were included. Meta-analysis was performed using Stata 15.1 to synthesize the results.ResultsThe analysis ultimately included 25 studies involving a total of 163,367 patients: 84,362 received sugammadex, while 79,005 received neostigmine, or did not receive an antagonist.Meta-analysis revealed a significant reduction in the incidence of POUR with sugammadex use (Relative Risk (RR): 0.47, 95% Confidence Interval (CI): 0.34-0.64, P ConclusionThese findings suggest that sugammadex substantially reduces POUR incidence, with no significant impact on POPS or 30-day readmission rates. Further research is warranted to explore its role in diverse patient populations and surgical procedures and to investigate its potential influence on postoperative pain management and readmission rates.
Abstract licence: CC BY-NC-ND
Ping-Cheng Shih, Han-Yu Lin, Po-Chuan Yu, et al.
BMC Anesthesiology, 2026
- Intraocular Pressure
- Sugammadex
- Neostigmine
Martins de Brito H, Ferraz Pozzer Gularte D, de Queiroz Vasconcelos V, et al.
2026
Postoperative cognitive dysfunction is a major clinical concern, particularly in elderly patients, leading to reduced quality of life and increased mortality. The impact of neuromuscular blockade reversal agents, such as sugammadex and neostigmine, on cognitive recovery remains uncertain. A systematic search of PubMed, EMBASE, and Cochrane databases identified randomized controlled trials (RCTs) and observational studies comparing sugammadex and neostigmine (± anticholinergics) for reversal of neuromuscular blockade in adults under general anesthesia for elective surgery. Studies published up to February 2025 that used the Mini-Mental State Examination (MMSE) or the cognitive domain of the Postoperative Quality Recovery Scale (PQRS) were included, as they both evaluate cognition on multiple aspects. Standardized mean differences (SMD) and standard errors (SE) were calculated, and a meta-analysis using the generic inverse variance method was performed. Heterogeneity was assessed with the I² statistic. Six RCTs and three observational studies, including 1,116 patients, were analyzed. Sugammadex was associated with better early cognitive recovery (40 to 60 minutes postoperatively) compared to neostigmine (SMD 0.20; 95% CI (0.07, 0.33); p = 0.003). No significant cognitive differences were observed immediately (≤15 minutes), on day one, or on days three to seven postoperatively. Sugammadex also improved physiological recovery at 40 minutes (RR 1.20; 95% CI (1.09, 1.30); p < 0.0001). Sensitivity analysis confirmed these findings. No differences were found in nociceptive, emotive, activities of daily living, or overall recovery domains. Sugammadex may improve early postoperative cognitive and physiological recovery over neostigmine, which could lead to a faster post-anesthesia care unit (PACU) discharge. No differences were observed at other time points or PQRS domains.
Abstract licence: CC BY
Tian L, Wang Y, Bu Y, et al.
2026
BackgroundPostoperative pulmonary complications (PPCs) remain common after video-assisted thoracoscopic (VATS) lung surgery. Whether sugammadex reduces the incidence of PPCs compared with traditional antagonists remains uncertain. This meta-analysis aimed to evaluate the impact of sugammadex on PPCs in patients undergoing VATS pulmonary resection.MethodsThis meta-analysis was conducted in accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA 2020). PubMed, Web of Science, Cochrane Library, and CNKI were searched from inception to December 13, 2024. Randomized controlled trials (RCTs) and cohort studies comparing sugammadex with other antagonists (e.g., neostigmine or pyridostigmine) in patients undergoing VATS pulmonary resection were included. The primary outcome was overall PPCs. Risk of bias was assessed using the Cochrane risk-of-bias tool for RCTs and the Newcastle-Ottawa Scale (NOS) for cohort studies. Odds ratios (ORs) with 95% confidence intervals (CIs) were pooled using fixed- or random-effects models according to heterogeneity.ResultsNine studies involving 2,240 patients were included, of which eight reported data on overall PPCs and were included in the primary meta-analysis. Sugammadex significantly reduced the incidence of overall PPCs compared with control agents (OR = 0.68, 95% CI: 0.58-0.80, P ConclusionsSugammadex may effectively reduce the risk of PPCs, particularly atelectasis, in patients undergoing VATS pulmonary resection. Further large-scale, high-quality studies are warranted.
Abstract licence: CC BY
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
82 found
Half-life
2 hours
Mechanism
Sugammadex is a modified gamma-cyclodextrin which forms very tight water soluble…
Food interactions
None known
Human targets
None mapped
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
Half-life
2 hours
Protein binding
Volume of distribution
11-14 L
Metabolism
Elimination
24 hours
Clearance
88L
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
[L52335]
Known interactions with other medicines. Always consult a healthcare professional.
Showing 50 of 104 interactions
How the body processes this drug — absorption, distribution, metabolism, and elimination
ATC V03AB35
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)
Sugammadex
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