Adverse Drug Reaction Classification System

         

Pharmaceutical Information
Drug Name Aminocaproic acid
Drug ID BADD_D00106
Description An antifibrinolytic agent that acts by inhibiting plasminogen activators which have fibrinolytic properties.
Indications and Usage For use in the treatment of excessive postoperative bleeding.
Marketing Status approved; investigational
ATC Code B02AA01
DrugBank ID DB00513
KEGG ID D00160
MeSH ID D015119
PubChem ID 564
TTD Drug ID D0FD0H
NDC Product Code 59285-019; 69766-054; 0517-9120; 0517-9191; 72205-049; 47621-310; 60687-529; 69238-1637; 69539-161; 69680-116; 80005-128; 46438-0641; 54288-151; 60687-739; 0404-9812; 69680-115; 70377-104; 76055-0030; 17478-447; 49411-050; 80005-129; 65571-0025; 70966-0010; 31722-035; 42799-054; 49411-052; 0409-4346; 62559-225; 69238-1596; 73216-110; 71052-265; 17478-768; 59651-573; 60687-724; 66689-330; 70377-102; 70377-103; 80005-130; 17478-769; 73216-111; 0904-7165; 72572-015; 49411-051; 51672-4226; 52817-815
UNII U6F3787206
Synonyms Aminocaproic Acid | 6-Aminohexanoic Acid | 6 Aminohexanoic Acid | epsilon-Aminocaproic Acid | epsilon Aminocaproic Acid | 6-Aminocaproic Acid | 6 Aminocaproic Acid | Capralense | Capramol | Caproamin | Caprocid | Hexalense | CY-116 | CY 116 | CY116 | Epsamon | Epsikapron | Hemocaprol | Amicar | Caprolest
Chemical Information
Molecular Formula C6H13NO2
CAS Registry Number 60-32-2
SMILES C(CCC(=O)O)CCN
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 pain07.01.05.002--
Agranulocytosis01.02.03.001--Not Available
Anaphylactic reaction24.06.03.006; 10.01.07.001--
Anaphylactic shock24.06.02.004; 10.01.07.002--Not Available
Anaphylactoid reaction24.06.03.007; 10.01.07.003--Not Available
Anxiety19.06.02.0020.000229%
Blood creatine phosphokinase increased13.04.01.001--
Blood urea increased13.13.01.006--Not Available
Bradycardia02.03.02.002--Not Available
Cerebrovascular accident24.03.05.001; 17.08.01.007--
Coagulopathy01.01.02.001--Not Available
Confusional state19.13.01.001; 17.02.03.005--
Delirium19.13.02.001--
Dermatitis23.03.04.002--Not Available
Diarrhoea07.02.01.001--
Discomfort08.01.08.003--Not Available
Dizziness02.11.04.006; 24.06.02.007; 17.02.05.0030.000846%
Drug hypersensitivity10.01.01.0010.000777%Not Available
Drug ineffective08.06.01.0060.000846%Not Available
Dyspnoea02.11.05.003; 22.02.01.004--
Ejaculation disorder21.03.01.002--
Epistaxis24.07.01.005; 22.04.03.0010.001966%
Erythema23.03.06.0010.000229%Not Available
Feeling abnormal08.01.09.014--Not Available
Flushing23.06.05.003; 08.01.03.025; 24.03.01.0020.000777%
Gastrointestinal pain07.01.05.005--
Gingival bleeding24.07.02.010; 07.09.07.0010.000343%Not Available
Haemarthrosis24.07.01.046; 15.01.01.004; 12.04.03.0010.000686%Not Available
Hallucination19.10.04.003--
Headache17.14.01.001--
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ADReCS-Target
Drug Name ADR Term Target
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