Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Trandolapril
Drug ID BADD_D02259
Description Trandolapril is a non-sulhydryl prodrug that belongs to the angiotensin-converting enzyme (ACE) inhibitor class of medications. It is metabolized to its biologically active diacid form, trandolaprilat, in the liver. Trandolaprilat inhibits ACE, the enzyme responsible for the conversion of angiotensin I (ATI) to angiotensin II (ATII). ATII regulates blood pressure and is a key component of the renin-angiotensin-aldosterone system (RAAS). Trandolapril may be used to treat mild to moderate hypertension, to improve survival following myocardial infarction in clinically stable patients with left ventricular dysfunction, as an adjunct treatment for congestive heart failure, and to slow the rate of progression of renal disease in hypertensive individuals with diabetes mellitus and microalbuminuria or overt nephropathy.
Indications and Usage For the treatment of mild to moderate hypertension, as an adjunct in the treatment of congestive heart failure (CHF), to improve survival following myocardial infarction (MI) in individuals who are hemodynamically stable and demonstrate symptoms of left ventricular systolic dysfunction or signs of CHF within a few days following acute MI, and to slow progression of renal disease in hypertensive patients with diabetes mellitus and microalbuminuria or overt nephropathy.
Marketing Status approved
ATC Code C09AA10
DrugBank ID DB00519
KEGG ID D00383
MeSH ID C052035
PubChem ID 5484727
TTD Drug ID D0M5OC
NDC Product Code 65862-165; 57237-089; 50370-0004; 65862-386; 63629-8003; 71335-1431; 57237-090; 68180-567; 65862-164; 66039-811; 68180-566; 68180-568; 65862-166; 57237-091; 63827-0003
UNII 1T0N3G9CRC
Synonyms trandolapril | 1-(2-((1-(ethoxycarbonyl)-3-phenylpropyl)amino)-1-oxopropyl)octahydro-1H-indol-2-carboxylic acid | Odrik | Udrik | RU 44570 | RU44570 | RU-44570 | Mavik | Gopten
Chemical Information
Molecular Formula C24H34N2O5
CAS Registry Number 87679-37-6
SMILES CCOC(=O)C(CCC1=CC=CC=C1)NC(C)C(=O)N2C3CCCCC3CC2C(=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)
Abdominal distension07.01.04.001--
Abdominal pain07.01.05.002--
Agitation17.02.05.012; 19.06.02.001--
Agranulocytosis01.02.03.001---
Alanine aminotransferase increased13.03.04.005--
Alopecia23.02.02.001--
Anaemia01.03.02.001--
Angina pectoris02.02.02.002; 24.04.04.002--
Angioedema10.01.05.009; 22.04.02.008; 23.04.01.001---
Anxiety19.06.02.002--
Apathy19.04.04.002---
Arrhythmia02.03.02.001---
Arrhythmia supraventricular02.03.03.001---
Arthralgia15.01.02.001--
Arthritis15.01.01.001--
Aspartate aminotransferase increased13.03.04.011--
Asthenia08.01.01.001---
Atrial fibrillation02.03.03.002--
Atrial flutter02.03.03.003--
Atrioventricular block02.03.01.002---
Atrioventricular block first degree02.03.01.004--
Azotaemia20.01.01.001---
Back pain15.03.04.005--
Blepharitis06.04.04.001; 23.03.04.012---
Blood creatinine decreased13.13.01.003---
Blood creatinine increased13.13.01.004--
Blood potassium increased13.11.01.011---
Blood pressure fluctuation24.06.01.002---
Blood urea increased13.13.01.006---
Blood uric acid increased13.02.04.001---
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ADReCS-Target
Drug Name ADR Term Target
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