Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Enalaprilat
Drug ID BADD_D00768
Description Enalaprilat is the active metabolite of the orally available pro-drug, [enalapril]. Used in the treatment of hypertension, enalapril is an ACE inhibitor that prevents Angiotensin Converting Enzyme (ACE) from transforming angiotensin I into angiotensin II. As angiotensin II is responsible for vasoconstriction and sodium reabsorption in the proximal tubule of the kidney, down-regulation of this protein results in reduced blood pressure and blood fluid volume. Enalaprilat was originally created to overcome the limitations of the first ACE inhibitor, captopril, which had numerous side effects and left a metallic taste in the mouth. Removal of the problematic thiol group from captopril resulted in enalaprilat, which was then modified further with an ester to create the orally available pro-drug enalapril. Enalaprilat is poorly orally available and is therefore only available as an intravenous injection for the treatment of hypertension when oral therapy is not possible.
Indications and Usage Enalaprilat injection is indicated for the treatment of hypertension when oral therapy is not practical.
Marketing Status approved
ATC Code Not Available
DrugBank ID DB09477
KEGG ID D03769
MeSH ID D015773
PubChem ID 5462501
TTD Drug ID D0N5HJ
NDC Product Code 51662-1477; 0143-9786; 43598-078; 71796-040; 43598-169; 0143-9787
UNII Q508Q118JM
Synonyms Enalaprilat | Enalaprilic Acid | Enalaprilat Dihydrate | Enalaprilat Citrate, Anhydrous | Enalaprilat, (R)-Isomer, Anhydrous | Pres iv | Vasotec | Enalaprilat Anhydrous | Xanef | 1-(N-((S)-1-Carboxy-3-phenylpropyl)-L-alanyl)-L-proline dihydrate | MK-422 | MK 422 | MK422
Chemical Information
Molecular Formula C18H24N2O5
CAS Registry Number 76420-72-9
SMILES CC(C(=O)N1CCCC1C(=O)O)NC(CCC2=CC=CC=C2)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)
Abdominal distension07.01.04.0010.004052%
Abdominal pain07.01.05.0020.018236%
Abnormal dreams19.02.03.001; 17.15.02.001--Not Available
Acidosis hyperchloraemic14.01.01.0070.002026%Not Available
Actinic keratosis23.01.06.0010.003039%Not Available
Acute febrile neutrophilic dermatosis23.03.03.033; 01.02.01.0060.006079%Not Available
Acute hepatic failure09.01.03.0010.002026%Not Available
Acute myocardial infarction24.04.04.001; 02.02.02.0010.004052%Not Available
Acute respiratory failure14.01.04.004; 22.02.06.0010.005065%Not Available
Ageusia17.02.07.001; 07.14.03.0030.002026%Not Available
Alkalosis14.01.02.0010.002026%
Alopecia23.02.02.001--
Anaemia01.03.02.0010.014183%
Anaemia macrocytic14.12.01.002; 01.03.02.0020.002026%Not Available
Anaphylactic reaction24.06.03.006; 10.01.07.0010.009523%
Anaphylactic shock24.06.02.004; 10.01.07.0020.003039%Not Available
Anaphylactoid reaction24.06.03.007; 10.01.07.003--Not Available
Angina pectoris24.04.04.002; 02.02.02.0020.004052%
Angina unstable24.04.04.004; 02.02.02.0040.003039%Not Available
Angioedema22.04.02.008; 23.04.01.001; 10.01.05.0090.182965%Not Available
Anosmia22.04.03.006; 17.04.04.001--
Anuria20.01.03.0020.007092%Not Available
Apathy19.04.04.0020.004052%Not Available
Aphasia19.21.01.001; 17.02.03.0010.002026%
Aphonia22.12.03.001; 19.19.01.002; 17.02.08.0090.002026%
Arrhythmia02.03.02.0010.003039%Not Available
Arthralgia15.01.02.001--
Arthritis15.01.01.0010.002026%
Asphyxia22.02.02.001; 12.01.08.0110.004052%Not Available
Asthenia08.01.01.001--Not Available
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ADReCS-Target
Drug Name ADR Term Target
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