Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Iopromide
Drug ID BADD_D01182
Description Iopromide is a low osmolar, non-ionic X-ray contrast agent for intravascular administration. It functions as a contrast agent by opacifying blood vessels in the path of flow of the contrast agent, permitting radiographic visualization of the internal structures until significant hemodilution occurs. Available as the FDA-approved product Ultravist, iopromide is used in radiographic studies such as intra-arterial digital subtraction angiography (IA-DSA), cerebral and peripheral arteriography, peripheral venography, excretory urography, brain computer tomography (CT), coronary arteriography, left ventriculography, visceral angiography, and aortography.
Indications and Usage Iopromide, as the product Iovist, is indicated for use as an X-ray contrast agent in the following procedures: Intra-arterial digital subtraction angiography (IA-DSA) (150 mg I/mL) Cerebral arteriography and peripheral arteriography (300 mg I/mL) Coronary arteriography and left ventriculography, visceral angiography and aortography (370 mg I/mL) Peripheral venography (240 mg I/mL) Excretory urography (300 mg I/mL) Contrast computed tomography (CT) imaging of head and body (300 mg I/mL and 370 mg I/mL)
Marketing Status approved
ATC Code V08AB05
DrugBank ID DB09156
KEGG ID D01893
MeSH ID C038192
PubChem ID 3736
TTD Drug ID D07GNP
NDC Product Code 50419-344; 50419-346; 50419-347; 50419-348
UNII 712BAC33MZ
Synonyms iopromide | lopromid | N,N'-bis(2,3-dihydroxypropyl)-2,4,6-triiodo-5-(2-methoxyacetamido)-N-methylisophthalamide | iopromid | Ultravist 300 | Clarograf | Ultravist
Chemical Information
Molecular Formula C18H24I3N3O8
CAS Registry Number 73334-07-3
SMILES CN(CC(CO)O)C(=O)C1=C(C(=C(C(=C1I)C(=O)NCC(CO)O)I)NC(=O)COC)I
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 discomfort07.01.06.001--Not Available
Abdominal pain07.01.05.002--
Abdominal pain upper07.01.05.003--
Acidosis14.01.03.0020.007113%
Acne23.02.01.0010.017783%Not Available
Acute myocardial infarction24.04.04.001; 02.02.02.0010.035567%Not Available
Acute pulmonary oedema22.01.03.005; 02.05.02.0040.024897%Not Available
Acute respiratory distress syndrome24.03.02.034; 10.02.01.067; 22.01.03.0010.007113%
Acute respiratory failure22.02.06.001; 14.01.04.0040.007113%Not Available
Agitation19.06.02.001; 17.02.05.0120.028454%
Altered state of consciousness19.07.01.003; 17.02.04.0010.049794%Not Available
Amaurosis06.02.10.0010.039124%Not Available
Amnesia19.20.01.001; 17.03.02.001--
Anaphylactic reaction24.06.03.006; 10.01.07.0010.212690%
Anaphylactic shock10.01.07.002; 24.06.02.0040.316546%Not Available
Anaphylactoid reaction24.06.03.007; 10.01.07.0030.028454%Not Available
Angina pectoris24.04.04.002; 02.02.02.0020.014227%
Angioedema10.01.05.009; 22.04.02.008; 23.04.01.0010.138000%Not Available
Anuria20.01.03.0020.010670%Not Available
Anxiety19.06.02.002--
Aphasia17.02.03.001; 19.21.01.0010.029876%
Aphonia22.12.03.001; 19.19.01.002; 17.02.08.0090.017783%
Apnoea22.02.01.0010.014227%
Arrhythmia02.03.02.0010.021340%Not Available
Arteriosclerosis coronary artery24.04.04.012; 02.02.01.0110.007113%Not Available
Arthralgia15.01.02.001--
Arthropathy15.01.01.003--Not Available
Asphyxia22.02.02.001; 12.01.08.0110.081804%Not Available
Asthenia08.01.01.001--Not Available
Asthma22.03.01.002; 10.01.03.010--Not Available
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ADReCS-Target
Drug Name ADR Term Target
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