Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Atracurium besylate
Drug ID BADD_D00188
Description A non-depolarizing neuromuscular blocking agent with short duration of action. Its lack of significant cardiovascular effects and its lack of dependence on good kidney function for elimination provide clinical advantage over alternate non-depolarizing neuromuscular blocking agents.
Indications and Usage For use, as an adjunct to general anesthesia, to facilitate endotracheal intubation and to provide skeletal muscle relaxation during surgery or mechanical ventilation.
Marketing Status Prescription; Discontinued
ATC Code M03AC04
DrugBank ID DB00732
KEGG ID D00758
MeSH ID D001279
PubChem ID 47320
TTD Drug ID D0Q1PR
NDC Product Code 55486-1597; 17404-0008; 0409-1105; 25021-672; 55150-216; 71288-701; 0409-1109; 55150-217; 71288-702; 25021-659
Synonyms Atracurium | 33 A 74 | A 74, 33 | Relatrac | Tracrium | BW-33A | BW 33A | BW33A | Atracurium Besylate | Atracurium Besilate | Besilate, Atracurium | Atracurium Dibesylate
Chemical Information
Molecular Formula C65H82N2O18S2
CAS Registry Number 64228-81-5
SMILES C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)OC)OC)OC)CCC(=O)OCCCCCOC(=O)CC[N+]4(CC C5=CC(=C(C=C5C4CC6=CC(=C(C=C6)OC)OC)OC)OC)C.C1=CC=C(C=C1)S(=O)(=O)[O-].C1=CC=C(C =C1)S(=O)(=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)
Anaphylactic shock24.06.02.004; 10.01.07.002--Not Available
Anaphylactoid reaction24.06.03.007; 10.01.07.003--Not Available
Angioedema23.04.01.001; 10.01.05.009--Not Available
Bradycardia02.03.02.002--Not Available
Bronchospasm22.03.01.004; 10.01.03.012--
Cardiac arrest02.03.04.001--
Cardiovascular disorder24.03.02.009; 02.01.01.001--Not Available
Dermatitis23.03.04.002--Not Available
Dyspnoea22.02.01.004; 02.01.03.002--
Erythema23.03.06.001--Not Available
Flushing24.03.01.002; 23.06.05.003; 08.01.03.025--
Heart rate decreased13.14.04.001--Not Available
Heart rate increased13.14.04.002--Not Available
Hypersensitivity10.01.03.003--
Hypertension24.08.02.001--
Hypotension24.06.03.002--
Hypoxia22.02.02.003--
Injection site reaction12.07.03.015; 08.02.03.014--
Laryngospasm22.04.02.002--
Mean arterial pressure13.14.03.018--Not Available
Mean arterial pressure decreased13.14.03.016--Not Available
Mean arterial pressure increased13.14.03.015--Not Available
Muscular weakness17.05.03.005; 15.05.06.001--
Myopathy15.05.05.001--Not Available
Neuromuscular block prolonged17.05.04.005; 12.02.12.004--Not Available
Neuromuscular blockade17.05.04.003--Not Available
Pruritus23.03.12.001--
Rash23.03.13.001--Not Available
Seizure17.12.03.001--
Tachycardia02.03.02.007--Not Available
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