Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Ketamine
Drug ID BADD_D01228
Description Ketamine is an NMDA receptor antagonist with a potent anesthetic effect.[A31869] It was developed in 1963 as a replacement for phencyclidine (PCP) by Calvin Stevens at Parke Davis Laboratories. It started being used for veterinary purposes in Belgium and in 1964 was proven that compared to PCP, it produced minor hallucinogenic effects and shorter psychotomimetic effects. It was FDA approved in 1970, and from there, it has been used as an anesthetic for children or patients undergoing minor surgeries but mainly for veterinary purposes.[L1332]
Indications and Usage Ketamine is indicated as an anesthetic agent for recommended diagnostic and surgical procedures. If skeletal muscle relaxation is needed, it should be combined with a muscle relaxant. If the surgical procedure involves visceral pain, it should be supplemented with an agent that obtunds visceral pain. Ketamine can be used for induction of anesthesia prior other general anesthetic agents and as a supplement of low potency agents.[L1336, FDA label] Reports have indicated a potential use of ketamine as a therapeutic tool for the management of depression when administered in lower doses.[A31873] These reports have increased the interest for ketamine in this area and several clinical trials are launched for this indication.[L1337, A31874]
Marketing Status approved; vet_approved
ATC Code N01AX03
DrugBank ID DB01221
KEGG ID D08098
MeSH ID D007649
PubChem ID 3821
TTD Drug ID D0UM7O
NDC Product Code Not Available
UNII 690G0D6V8H
Synonyms Ketamine | 2-(2-Chlorophenyl)-2-(methylamino)cyclohexanone | CI-581 | CI 581 | CI581 | Ketalar | Ketaset | Ketanest | Calipsol | Kalipsol | Calypsol | Ketamine Hydrochloride
Chemical Information
Molecular Formula C13H16ClNO
CAS Registry Number 6740-88-1
SMILES CNC1(CCCCC1=O)C2=CC=CC=C2Cl
Chemical Structure
ADRs Induced by Drug
*The priority for ADR severity classification is based on FAERS assessment, followed by the most severe level in CTCAE rating. If neither is available, it will be displayed as 'Not available'.
**The 'Not Available' level is hidden by default and can be restored by clicking on the legend twice.
ADR Term ADReCS ID ADR Frequency (FAERS) ADR Severity Grade (FAERS) ADR Severity Grade (CTCAE)
Abdominal pain07.01.05.0020.000714%
Abdominal pain upper07.01.05.0030.000536%
Acidosis14.01.03.0020.000268%
Anaphylactic shock10.01.07.002; 24.06.02.0040.000179%-
Anxiety19.06.02.0020.000357%
Apnoea22.02.01.001--
Arrhythmia02.03.02.001---
Ataxia08.01.02.004; 17.02.02.0010.000179%
Atrial fibrillation02.03.03.0020.000179%
Biliary colic09.02.01.0010.000179%-
Bladder neck obstruction20.03.01.0100.000357%-
Bladder pain20.02.02.001---
Bradycardia02.03.02.0020.000357%-
Bronchospasm10.01.03.012; 22.03.01.0040.000268%
Cardiac arrest02.03.04.0010.000714%
Cardio-respiratory arrest02.03.04.002; 22.02.06.0070.000357%-
Cholangitis09.02.01.0020.000179%-
Cholangitis sclerosing09.02.01.003; 10.04.09.0020.000357%-
Clonus17.02.05.002---
Completed suicide08.04.01.010; 19.12.01.0010.000447%-
Condition aggravated08.01.03.0040.000357%-
Contracted bladder20.03.03.0050.000536%-
Cystitis11.01.14.001; 20.03.02.002--
Cystitis haemorrhagic20.03.02.0030.000179%-
Cystitis interstitial10.02.01.039; 20.03.02.0050.001786%-
Death08.04.01.0010.002411%
Delirium19.13.02.0010.000268%
Dermatitis23.03.04.002---
Diabetes insipidus05.03.03.004; 14.05.07.0030.000268%-
Diplopia06.02.06.002; 17.17.01.005---
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ADReCS-Target
Drug Name ADR Term Target
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