Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Deferoxamine mesylate
Drug ID BADD_D00597
Description Natural product isolated from Streptomyces pilosus. It forms iron complexes and is used as a chelating agent, particularly in the mesylate form.
Indications and Usage Used to treat acute iron or aluminum toxicity (an excess of aluminum in the body) in certain patients. Also used in certain patients with anemia who must receive many blood transfusions.
Marketing Status Prescription; Discontinued
ATC Code V03AC01
DrugBank ID DB00746
KEGG ID D01186
MeSH ID D003676
PubChem ID 62881
TTD Drug ID D0FJ8A
NDC Product Code 68083-173; 68083-172; 63323-597; 63323-599; 47781-624; 0409-2337; 0078-0467; 60505-6236; 60505-6238; 17337-0060; 46014-1003; 60505-6237; 51846-1016; 46014-1127
Synonyms Deferoxamine | Desferrioxamine | Desferioximine | Deferoxamine B | Desferrioxamine B | Deferoximine | Deferrioxamine B | Desferroxamine | Desferrioxamine B Mesylate | Mesylate, Desferrioxamine B | Deferoxamine Mesilate | Mesilate, Deferoxamine | Deferoxamine Mesylate | Mesylate, Deferoxamine | Deferoxamine Methanesulfonate | Methanesulfonate, Deferoxamine | Desferal
Chemical Information
Molecular Formula C26H52N6O11S
CAS Registry Number 138-14-7
SMILES CC(=O)N(CCCCCNC(=O)CCC(=O)N(CCCCCNC(=O)CCC(=O)N(CCCCCN)O)O)O.CS(=O)(=O)O
Chemical Structure
ADR Related Proteins Induced by Drug
ADR Term Protein Name UniProt AC TTD Target ID PMID
Not AvailableNot AvailableNot AvailableNot AvailableNot Available
ADRs Induced by Drug
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--
Acute respiratory distress syndrome22.01.03.001--
Anaphylactic reaction24.06.03.006; 10.01.07.001--
Angioedema23.04.01.001; 10.01.05.009--Not Available
Arthralgia15.01.02.001--
Asthma22.03.01.002; 10.01.03.010--Not Available
Blindness17.17.01.003; 06.02.02.001--Not Available
Blister23.03.01.001; 12.01.06.002--Not Available
Burning sensation08.01.09.029; 17.02.06.001--Not Available
Cataract06.06.01.001--
Chromatopsia06.02.05.001--Not Available
Deafness neurosensory17.04.07.001; 04.02.01.002--Not Available
Diarrhoea07.02.01.001--
Dizziness17.02.05.003; 02.01.02.004; 24.06.02.007--
Dysuria20.02.02.002--
Encephalopathy17.13.02.001--
Erythema23.03.06.001--Not Available
Headache17.14.01.001--
Hypotension24.06.03.002--
Injection site extravasation08.02.03.002; 12.07.03.002--Not Available
Iris atrophy06.06.06.004--Not Available
Muscle spasms15.05.03.004--
Myalgia15.05.02.001--
Nausea07.01.07.001--
Neuropathy peripheral17.09.03.003--Not Available
Night blindness14.12.03.001; 06.02.02.003--
Optic neuritis17.04.05.001; 10.04.10.002; 06.04.08.002--Not Available
Pain08.01.08.004--
Paraesthesia17.02.06.005--
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