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)
Abdominal pain07.01.05.002--
Abnormal dreams19.02.03.001; 17.15.02.001--Not Available
Acidosis14.01.03.0020.002759%
Acute hepatic failure09.01.03.0010.000617%Not Available
Acute respiratory distress syndrome22.01.03.0010.000617%
Acute respiratory failure22.02.06.001; 14.01.04.0040.001028%Not Available
Aggression19.05.01.0010.001182%Not Available
Agitation19.06.02.001; 17.02.05.0120.014187%
Alanine aminotransferase increased13.03.01.003--
Amaurosis06.02.02.0080.000788%Not Available
Amblyopia06.02.01.001--Not Available
Anaemia01.03.02.001--
Anaesthetic complication neurological17.02.10.015; 12.02.12.0090.000788%Not Available
Anaesthetic complication pulmonary22.02.07.005; 12.02.12.0070.001970%Not Available
Anaphylactic reaction24.06.03.006; 10.01.07.0010.009458%
Anaphylactic shock24.06.02.004; 10.01.07.0020.031526%Not Available
Anaphylactoid reaction24.06.03.007; 10.01.07.0030.001182%Not Available
Angioedema10.01.05.009; 23.04.01.0010.001970%Not Available
Anticholinergic syndrome17.05.01.001--Not Available
Anxiety19.06.02.002--
Apnoea22.02.01.0010.003941%
Arrhythmia02.03.02.0010.000411%Not Available
Arrhythmia supraventricular02.03.03.001--Not Available
Arthralgia15.01.02.001--
Aspartate aminotransferase increased13.03.01.0060.001576%
Aspiration22.02.07.0070.001234%
Asthenia08.01.01.001--Not Available
Athetosis17.01.01.004--Not Available
Atrial fibrillation02.03.03.0020.003547%
Atrioventricular block02.03.01.0020.000788%Not Available
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