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Sugammadex information


Sugammadex
Clinical data
Pronunciationsoo GAM ma dex
Trade namesBridion
Other namesORG-25969
AHFS/Drugs.comMonograph
License data
  • US DailyMed: Sugammadex
Pregnancy
category
  • AU: B2
Routes of
administration
Intravenous
ATC code
  • V03AB35 (WHO)
Legal status
Legal status
  • AU: S4 (Prescription only)[1][2]
  • CA: ℞-only[3]
  • UK: POM (Prescription only)[4]
  • US: ℞-only[5]
  • EU: Rx-only[6][7]
  • In general: ℞ (Prescription only)
Identifiers
CAS Number
  • 343306-71-8 ☒N
PubChem CID
  • 6918585
  • as salt: 6918584
DrugBank
  • DB06206 checkY
ChemSpider
  • 32689915 ☒N
UNII
  • 361LPM2T56
  • as salt: ERJ6X2MXV7 checkY
KEGG
  • as salt: D05940 checkY
ChEBI
  • CHEBI:90953 ☒N
  • as salt: CHEBI:90952 ☒N
ChEMBL
  • ChEMBL2111107
  • as salt: ChEMBL2107374
ECHA InfoCard100.121.931 Edit this at Wikidata
Chemical and physical data
FormulaC72H112O48S8
Molar mass2002.12 g·mol−1
3D model (JSmol)
  • Interactive image
SMILES
  • O=C(O)CCSC[C@H]1O[C@@H]2O[C@@H]3[C@@H](CSCCC(=O)O)O[C@H](O[C@@H]4[C@@H](CSCCC(=O)O)O[C@H](O[C@@H]5[C@@H](CSCCC(=O)O)O[C@H](O[C@@H]6[C@@H](CSCCC(=O)O)O[C@H](O[C@@H]7[C@@H](CSCCC(=O)O)O[C@H](O[C@@H]8[C@@H](CSCCC(=O)O)O[C@H](O[C@@H]9[C@@H](CSCCC(=O)O)O[C@H](O[C@H]1[C@H](O)[C@H]2O)[C@H](O)[C@H]9O)[C@H](O)[C@H]8O)[C@H](O)[C@H]7O)[C@H](O)[C@H]6O)[C@H](O)[C@H]5O)[C@H](O)[C@H]4O)[C@H](O)[C@H]3O
InChI
  • InChI=1S/C72H112O48S8/c73-33(74)1-9-121-17-25-57-41(89)49(97)65(105-25)114-58-26(18-122-10-2-34(75)76)107-67(51(99)43(58)91)116-60-28(20-124-12-4-36(79)80)109-69(53(101)45(60)93)118-62-30(22-126-14-6-38(83)84)111-71(55(103)47(62)95)120-64-32(24-128-16-8-40(87)88)112-72(56(104)48(64)96)119-63-31(23-127-15-7-39(85)86)110-70(54(102)46(63)94)117-61-29(21-125-13-5-37(81)82)108-68(52(100)44(61)92)115-59-27(19-123-11-3-35(77)78)106-66(113-57)50(98)42(59)90/h25-32,41-72,89-104H,1-24H2,(H,73,74)(H,75,76)(H,77,78)(H,79,80)(H,81,82)(H,83,84)(H,85,86)(H,87,88)/t25-,26-,27-,28-,29-,30-,31-,32-,41-,42-,43-,44-,45-,46-,47-,48-,49-,50-,51-,52-,53-,54-,55-,56-,57-,58-,59-,60-,61-,62-,63-,64-,65-,66-,67-,68-,69-,70-,71-,72-/m1/s1 ☒N
  • Key:WHRODDIHRRDWEW-VTHZAVIASA-N ☒N
 ☒NcheckY (what is this?)  (verify)

Sugammadex, sold under the brand name Bridion, is a medication for the reversal of neuromuscular blockade induced by rocuronium and vecuronium[5] in general anaesthesia. It is the first selective relaxant binding agent (SRBA). It is marketed by Merck.[8]

The most common side effects include cough, airway problems due to the anaesthesia wearing off, reduced blood pressure and other complications such as changes in heart rate.[6]

Sugammadex is available as a generic medication.[9]

  1. ^ SUGAMMADEX ACCORD (Accord Healthcare Pty Ltd) Archived 2022-10-12 at the Wayback Machine Department of Health and Aged Care. Retrieved 30 March 2023
  2. ^ SUGAMMADEX SANDOZ (Sandoz Pty Ltd) Archived 2022-10-12 at the Wayback Machine Department of Health and Aged Care. Retrieved 30 March 2023
  3. ^ "Health Canada New Drug Authorizations: 2016 Highlights". Health Canada. 14 March 2017. Retrieved 7 April 2024.
  4. ^ "Bridion 100 mg/ml solution for injection - Summary of Product Characteristics (SmPC)". (emc). 18 March 2021. Archived from the original on 27 June 2021. Retrieved 27 June 2021.
  5. ^ a b Cite error: The named reference Bridion FDA label was invoked but never defined (see the help page).
  6. ^ a b "Bridion EPAR". European Medicines Agency (EMA). 17 September 2018. Archived from the original on 10 June 2020. Retrieved 10 June 2020. Text was copied from this source which is © European Medicines Agency. Reproduction is authorized provided the source is acknowledged.
  7. ^ "Sugammadex Adroiq". Union Register of medicinal products. 30 May 2023. Retrieved 6 June 2023.
  8. ^ "Dosing for Bridion (sugammadex)". www.merckconnect.com. Archived from the original on 2019-01-12. Retrieved 2019-01-11.
  9. ^ "Sugammadex Adroiq". European Medicines Agency. 16 June 2023. Retrieved 19 June 2023.

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Sugammadex

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Sugammadex, sold under the brand name Bridion, is a medication for the reversal of neuromuscular blockade induced by rocuronium and vecuronium in general...

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Rocuronium bromide

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derivative sugammadex (trade name Bridion) is an agent to reverse the action of rocuronium by binding to it with high affinity. Sugammadex has been in...

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Vecuronium bromide

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of acetylcholine on skeletal muscles. The effects may be reversed with sugammadex or a combination of neostigmine and glycopyrrolate. To minimize residual...

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Rapid sequence induction

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possibility of waking the patient with paralytic reversal medications such as sugammadex. Conversely, the induction drugs classically used for RSI have short durations...

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Selective relaxant binding agents

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neuromuscular blocking agents (NMBAs). The first drug introduction of an SRBA is sugammadex. . SRBAs exert a chelating action that effectively terminates an NMBA...

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Anesthetic

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Neostigmine, helps to reverse the effects of non-depolarizing muscle relaxants Sugammadex, helps to reverse the effects of non-depolarizing muscle relaxants Goldberg...

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General anaesthesia

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such as sugammadex may also be used; it works by directly binding muscle relaxants and removing it from the neuromuscular junction. Sugammadex was approved...

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Postoperative residual curarization

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Neuromuscular function monitoring and the use of the appropriate dosage of sugammadex to reverse blockade produced by rocuronium can reduce the incidence of...

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ATC code V03

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V03AB32 Glutathione V03AB33 Hydroxocobalamin V03AB34 Fomepizole V03AB35 Sugammadex V03AB36 Phentolamine V03AB37 Idarucizumab V03AB38 Andexanet alfa V03AB54...

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Fred Hassan

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Prize was awarded to researchers for its work on a new anaesthesia drug, sugammadex.[failed verification] It currently employs 250 scientists across a range...

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