Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Propofol
Drug ID BADD_D01864
Description Propofol is an intravenous anaesthetic agent used for induction and maintenance of general anaesthesia. IV administration of propfol is used to induce unconsciousness after which anaesthesia may be maintained using a combination of medications. Recovery from propofol-induced anaesthesia is generally rapid and associated with less frequent side effects (e.g. drowsiness, nausea, vomiting) than with thiopental, methohexital, and etomidate. Propofol may be used prior to diagnostic procedures requiring anaesthesia, in the management of refractory status epilepticus, and for induction and/or maintenance of anaesthesia prior to and during surgeries.
Indications and Usage Used for induction and/or maintenance of anaesthesia and for management of refractory status epilepticus.
Marketing Status Prescription; Discontinued
ATC Code N01AX10
DrugBank ID DB00818
KEGG ID D00549
MeSH ID D015742
PubChem ID 4943
TTD Drug ID D0A3HB
NDC Product Code 72572-612; 69135-0010; 52584-699; 0409-4699; 50090-4569; 0641-6194; 25021-608; 63323-269; 0069-0209; 0069-0234; 51504-0003; 58032-2019; 51662-1470; 14593-885; 51662-1471; 72572-583; 44657-0044; 70518-3256; 0591-2136; 72572-590; 0641-6195; 0641-6196; 72572-585; 72572-601; 51662-1293; 18124-027; 65219-427; 0069-0248; 65219-800; 23155-345; 72572-584; 0404-9943; 66064-1015; 52133-0023; 52584-098
Synonyms Propofol | 2,6-Diisopropylphenol | 2,6 Diisopropylphenol | 2,6-Bis(1-methylethyl)phenol | Disoprofol | Diprivan | Disoprivan | Fresofol | ICI-35,868 | ICI 35,868 | ICI35,868 | ICI-35868 | ICI 35868 | ICI35868 | Ivofol | Propofol Fresenius | Propofol MCT | Propofol Rovi | Propofol-Lipuro | Recofol | Aquafol | Propofol Abbott
Chemical Information
Molecular Formula C12H18O
CAS Registry Number 2078-54-8
SMILES CC(C)C1=C(C(=CC=C1)C(C)C)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)
Dry mouth07.06.01.002--
Dysarthria19.19.03.001; 17.02.08.0010.001182%
Dysgeusia07.14.03.001; 17.02.07.003--
Dyskinesia17.01.02.0060.003941%
Dysphagia07.01.06.003--
Dysphoria19.04.02.0040.000788%Not Available
Dyspnoea22.02.01.004; 02.01.03.002--
Dystonia17.01.03.0010.000788%Not Available
Ear pain04.03.01.003--
Electrocardiogram abnormal13.14.05.0010.001182%Not Available
Electrocardiogram QRS complex prolonged13.14.05.0030.000788%Not Available
Electrocardiogram ST segment abnormal13.14.05.0170.001182%Not Available
Electrocardiogram ST segment depression13.14.05.0050.001182%Not Available
Electrocardiogram ST segment elevation13.14.05.0250.000925%Not Available
Emotional disorder19.04.02.005--Not Available
Encephalopathy17.13.02.0010.001970%
Epilepsy17.12.03.0020.001576%Not Available
Erythema23.03.06.0010.008670%Not Available
Euphoric mood19.04.02.006--
Extrapyramidal disorder17.01.02.0070.000788%
Extrasystoles02.03.02.0030.000788%Not Available
Extravasation08.01.03.0080.007881%Not Available
Eye pain06.08.03.002--
Face oedema23.04.01.004; 10.01.05.002; 08.01.07.0030.001182%
Fatigue08.01.01.002--
Feeling abnormal08.01.09.014--Not Available
Feeling cold08.01.09.0080.000788%Not Available
Feeling hot08.01.09.0090.000788%Not Available
Feeling jittery08.01.09.0160.001182%Not Available
Flushing24.03.01.002; 23.06.05.003; 08.01.03.025--
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