Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Tranexamic acid
Drug ID BADD_D02261
Description Tranexamic acid is a synthetic derivative of [lysine] used as an antifibrinolytic in the treatment and prevention of major bleeding. It possesses a similar mechanism of action to [aminocaproic acid] but is approximately 10-fold more potent.[L31883] It was first patented in 1957[A230108] and received its initial US approval in 1986.[L31858]
Indications and Usage Taken orally, tranexamic acid is indicated for the treatment of hereditary angioedema,[L31883] cyclic heavy menstrual bleeding in premenopausal females,[L31858] and other instances of significant bleeding in the context of hyperfibrinolysis.[L31883] Given intravenously, tranexamic acid is indicated for short-term use (2-8 days) in patients with hemophilia to prevent or reduce bleeding following tooth extraction.[L31853]
Marketing Status approved
ATC Code B02AA02
DrugBank ID DB00302
KEGG ID D01136
MeSH ID D014148
PubChem ID 5526
TTD Drug ID D05HXX
NDC Product Code 51927-0022; 73309-178; 42571-189; 50268-772; 69918-301; 70771-1085; 0591-3720; 49452-7876; 51552-0513; 81999-0001; 82920-038; 70121-1398; 23155-524; 43066-008; 55150-188; 63629-8838; 67850-041; 68083-160; 71335-1981; 60505-6169; 65145-106; 0517-0960; 81284-611; 12079-2001; 62991-3131; 82920-045; 51662-1532; 63629-8599; 67457-197; 70860-400; 70860-407; 71335-1957; 81284-612; 14537-115; 65388-0156; 61990-0611; 67850-042; 38779-3211; 57218-951; 25021-415; 42571-314; 50090-5072; 63323-563; 68382-891; 72611-760; 12848-1004; 0013-1114; 69918-300; 49452-7877; 71052-166; 23155-166; 51754-0108; 62559-265; 72485-107; 38779-2794; 39822-1000
UNII 6T84R30KC1
Synonyms Tranexamic Acid | AMCHA | trans-4-(Aminomethyl)cyclohexanecarboxylic Acid | t-AMCHA | AMCA | Anvitoff | Cyklokapron | Ugurol | KABI 2161 | Spotof | Transamin | Amchafibrin | Exacyl
Chemical Information
Molecular Formula C8H15NO2
CAS Registry Number 701-54-2
SMILES C1CC(CCC1CN)C(=O)O
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)
Visual impairment06.02.10.0130.011535%Not Available
Vomiting07.01.07.003--
Wheezing22.03.01.0090.004676%
Cardiotoxicity12.03.01.007; 02.11.01.0090.006235%Not Available
Factor VIII inhibition01.01.02.0120.009352%Not Available
Intracardiac thrombus02.11.01.017; 24.01.05.0030.003117%Not Available
Poor venous access24.03.02.017--Not Available
Seasonal allergy22.04.04.008; 10.01.04.001; 06.04.01.013--Not Available
Brain oedema17.07.02.003; 12.01.10.0100.004676%
Allergic sinusitis10.01.03.021; 22.04.06.003--Not Available
Balance disorder08.01.03.081; 17.02.02.007--Not Available
Musculoskeletal chest pain22.09.01.001; 15.03.04.0120.003117%
Deep vein thrombosis24.01.02.0030.034292%Not Available
Acute coronary syndrome24.04.04.011; 02.02.02.015--Not Available
Haemodynamic instability24.03.02.0060.014029%Not Available
Musculoskeletal discomfort15.03.04.001--Not Available
Myoclonic epilepsy17.12.03.0070.014029%Not Available
Haemorrhage24.07.01.0020.052062%Not Available
Paraesthesia oral07.05.05.035; 17.02.06.0080.003117%Not Available
Cognitive disorder19.21.02.001; 17.03.03.0030.006235%
Venous occlusion24.04.02.009--Not Available
Angiopathy24.03.02.007--Not Available
Ischaemic cerebral infarction24.04.06.013; 17.08.01.0220.006235%Not Available
Cardiac disorder02.11.01.003--Not Available
Embolism24.01.01.0090.003117%
Infarction24.04.02.017--Not Available
Ischaemia24.04.02.004--Not Available
Ischaemic stroke24.04.06.010; 17.08.01.0180.029616%Not Available
Mediastinal disorder22.09.03.001--Not Available
Partial seizures17.12.03.0100.004676%Not Available
The 7th Page    First    Pre   7 8 9    Next   Last    Total 9 Pages