Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Ferumoxsil
Drug ID BADD_D00888
Description Not Available
Indications and Usage Not Available
Marketing Status approved; experimental
ATC Code V08CB01
DrugBank ID DB09507
KEGG ID D04175
MeSH ID C088769
PubChem ID Not Available
TTD Drug ID D0V7QT
NDC Product Code Not Available
UNII 6HJV9H13XS
Synonyms ferumoxsil | siloxane-coated superparamagnetic iron oxide | siloxane-coated SPIO | Lumirem | AMI 121 | AMI-121 | Gastromark
Chemical Information
Molecular Formula Not Available
CAS Registry Number 171544-35-7
SMILES Not Available
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 pain07.01.05.002--
Chills08.01.09.001; 15.05.03.016--
Diarrhoea07.02.01.001--
Dysgeusia07.14.03.001; 17.02.07.003--
Dyspepsia07.01.02.001--
Eructation07.01.02.003--
Flatulence07.01.04.002--
Headache17.14.01.001--
Nausea07.01.07.001--
Oedema peripheral02.05.04.007; 08.01.07.007; 14.05.06.011--
Pruritus23.03.12.001--
Pyrexia08.05.02.003--
Rash pustular11.01.12.002; 23.03.10.003--
Stomatitis07.05.06.005--
Urticaria10.01.06.001; 23.04.02.001--
Vomiting07.01.07.003--
Postoperative ileus07.02.05.004; 12.02.03.012---
Paraesthesia oral07.05.05.035; 17.02.06.008---
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