Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Sugammadex
Drug ID BADD_D02084
Description Sugammadex is a selective relaxant binding agent indicated for reversal of neuromuscular blockade induced by rocuronium bromide and vecuronium bromide during surgery in adults. Rocuronium bromide and vecuronium bromide are neuromuscular blocking medications that cause temporary paralysis and are especially useful for general anesthesia, ventilation, or tracheal intubation that patients may require for surgery. Sugammadex provides a new treatment option to reverse the effects of those medications and possibly help patients recover sooner post-surgery. Sugammadex (brand name Bridion) is marketed by Merck Sharp and Dohme, and was approved by the United States FDA on December 15, 2015.
Indications and Usage Sugammadex is indicated for the reversal of neuromuscular blockade induced by rocuronium bromide and vecuronium bromide in adults undergoing surgery.
Marketing Status Prescription
ATC Code V03AB35
DrugBank ID DB06206
KEGG ID D05940
MeSH ID D000077122
PubChem ID 6918585
TTD Drug ID D08RID
NDC Product Code 0006-5423; 48087-0153; 48087-0151; 71872-7187; 0006-5425; 63552-003; 58175-0618; 60870-0464; 63552-004
Synonyms Sugammadex | Org 25969 | Sugammadex Sodium | 6-Perdeoxy-6-per(2-carboxyethyl)thio-gamma-cyclodextrin sodium salt | Bridion
Chemical Information
Molecular Formula C72H112O48S8
CAS Registry Number 343306-71-8
SMILES C(CSCC1C2C(C(C(O1)OC3C(OC(C(C3O)O)OC4C(OC(C(C4O)O)OC5C(OC(C(C5O)O)OC6C(OC(C(C6O) O)OC7C(OC(C(C7O)O)OC8C(OC(C(C8O)O)OC9C(OC(O2)C(C9O)O)CSCCC(=O)O)CSCCC(=O)O)CSCCC (=O)O)CSCCC(=O)O)CSCCC(=O)O)CSCCC(=O)O)CSCCC(=O)O)O)O)C(=O)O
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Not AvailableNot AvailableNot AvailableNot AvailableNot Available
ADRs Induced by Drug
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Pruritus23.03.12.0010.008747%
Pulmonary oedema22.01.03.003; 02.05.02.0030.020409%
Pulse absent13.14.04.0050.008747%Not Available
Pyrexia08.05.02.003--
Rash23.03.13.001--Not Available
Rash erythematous23.03.06.003--Not Available
Red blood cell count decreased13.01.05.007--Not Available
Respiratory arrest22.02.01.0090.014578%Not Available
Respiratory depression22.02.01.010; 17.02.05.0470.014578%Not Available
Restlessness19.11.02.002; 17.02.05.021--
Shock24.06.02.0020.008747%Not Available
Stridor22.04.02.0030.005831%
Subcutaneous emphysema23.07.04.006; 12.02.06.0020.005831%
Supraventricular tachycardia02.03.03.012--
Swollen tongue23.04.01.014; 10.01.05.015; 07.14.02.003--Not Available
Tachycardia02.03.02.0070.017494%Not Available
Tongue oedema23.04.01.009; 10.01.05.008; 07.14.02.0070.005831%Not Available
Type I hypersensitivity10.01.03.0060.005831%Not Available
Unresponsive to stimuli17.02.05.0310.005831%Not Available
Urticaria10.01.06.001; 23.04.02.0010.008747%
Ventricular fibrillation02.03.04.0080.002282%
Ventricular tachycardia02.03.04.0100.005831%
Vomiting07.01.07.003--
Airway complication of anaesthesia22.02.07.006; 12.02.12.001--Not Available
Post procedural haemorrhage24.07.01.014; 12.02.05.0040.005831%
Wound haemorrhage24.07.01.029; 12.01.08.017--Not Available
Eye oedema06.08.03.0130.005831%Not Available
Procedural complication12.02.05.005--
Incision site pain08.01.08.008; 12.02.05.006--Not Available
Pulseless electrical activity02.03.04.0200.014578%Not Available
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