Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Hydralazine
Drug ID BADD_D01081
Description Originally developed in the 1950s as a malaria treatment, hydralazine showed antihypertensive ability and was soon repurposed.[A186841] Hydralazine is a hydrazine derivative vasodilator used alone or as adjunct therapy in the treatment of hypertension and only as adjunct therapy in the treatment of heart failure.[A186820,L8782,L8785] Hydralazine is no longer a first line therapy for these indications since the development of newer antihypertensive medications.[T691] Hydralazine hydrochloride was FDA approved on 15 January 1953.[L8779]
Indications and Usage Hydralazine is indicated alone or adjunct to standard therapy to treat essential hypertension.[L8782] A combination product with isosorbide dinitrate is indicated as an adjunct therapy in the treatment of heart failure.[L8785]
Marketing Status approved
ATC Code C02DB02
DrugBank ID DB01275
KEGG ID D08044
MeSH ID D006830
PubChem ID 3637
TTD Drug ID D0K1XK
NDC Product Code Not Available
UNII 26NAK24LS8
Synonyms Hydralazine | Hydrallazin | Hydrazinophthalazine | Apressin | Nepresol | Hydralazine mono-Hydrochloride | Hydralazine mono Hydrochloride | mono-Hydrochloride, Hydralazine | Apressoline | Apresoline | Hydralazine Hydrochloride | Hydrochloride, Hydralazine
Chemical Information
Molecular Formula C8H8N4
CAS Registry Number 86-54-4
SMILES C1=CC=C2C(=C1)C=NN=C2NN
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)
Pulmonary alveolar haemorrhage22.01.02.005; 24.07.01.0150.002386%-
Pulmonary haemorrhage22.12.01.009; 24.07.01.0160.000579%
Pulmonary oedema02.05.02.003; 22.01.03.0030.000170%
Purpura01.01.04.003; 23.06.01.004; 24.07.06.0050.000184%
Pyrexia08.05.02.003--
Rash23.03.13.001---
Rash morbilliform23.03.13.0050.000068%-
Renal failure20.01.03.0050.000341%-
Renal haemorrhage12.01.05.004; 20.01.02.013; 24.07.07.0020.000068%
Renal tubular necrosis20.01.07.0030.000102%-
Renal vasculitis10.02.02.013; 20.01.07.007; 24.12.04.0210.000750%-
Respiratory depression17.02.05.047; 22.02.01.0100.000068%-
Respiratory distress22.02.01.0120.000170%-
Respiratory failure14.01.04.003; 22.02.06.0020.000729%
Restlessness17.02.05.021; 19.11.02.0020.000150%
Retinal vasculitis06.04.06.011; 10.02.02.0210.000068%-
Retroperitoneal fibrosis07.07.03.003; 10.02.01.026; 20.06.01.006---
Sensory loss17.02.07.007---
Sinus tachycardia02.03.03.0100.000184%
Splenomegaly01.09.02.001---
Strangury20.02.02.017---
Supraventricular tachycardia02.03.03.0120.000170%
Systemic lupus erythematosus10.04.03.004; 15.06.02.003; 23.03.02.0060.001343%-
Systemic lupus erythematosus rash10.04.03.005; 15.06.02.005; 23.03.13.0070.000232%-
Tachycardia02.03.02.0070.000239%-
Thrombocytopenia01.08.01.002---
Tremor17.01.06.002--
Urinary retention20.02.02.011--
Urticaria10.01.06.001; 23.04.02.001--
Vascular purpura01.01.04.007; 23.06.01.008; 24.07.06.011---
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ADReCS-Target
Drug Name ADR Term Target
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