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)
Injection site pain08.02.03.010; 12.07.03.011--Not Available
Intestinal infarction07.15.02.006; 24.04.08.008--Not Available
Iron deficiency anaemia14.13.02.001; 01.03.01.0020.009976%Not Available
Joint stiffness15.01.02.003--Not Available
Joint swelling15.01.02.0040.009352%Not Available
Leukocytosis01.02.01.0020.003117%
Loss of consciousness17.02.04.0040.009352%Not Available
Low cardiac output syndrome02.05.01.0080.003117%Not Available
Malaise08.01.01.003--
Menstruation irregular21.01.01.005; 05.05.01.008--
Metabolic acidosis14.01.01.0030.003117%Not Available
Migraine17.14.02.001; 24.03.05.0030.010911%Not Available
Multiple allergies10.01.03.030--Not Available
Muscle haemorrhage12.01.07.016; 24.07.01.037; 15.05.03.0170.007794%Not Available
Muscle spasms15.05.03.004--
Muscle twitching15.05.03.0050.003117%Not Available
Muscular weakness17.05.03.005; 15.05.06.0010.010911%
Musculoskeletal pain15.03.04.0070.004676%
Myalgia15.05.02.001--
Myocardial infarction24.04.04.009; 02.02.02.0070.028057%
Myocardial ischaemia24.04.04.010; 02.02.02.008--Not Available
Myoclonus17.02.05.0080.052997%Not Available
Myopathy15.05.05.0010.003117%Not Available
Nausea07.01.07.001--
Neck pain15.03.04.0090.004676%
Nervous system disorder17.02.10.001--Not Available
Neurotoxicity17.02.10.002; 12.03.01.0110.017146%Not Available
Night blindness06.02.10.010; 14.12.03.0010.003117%
Nystagmus17.02.02.006; 06.05.02.0060.003117%
Pain08.01.08.004--
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