Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Dexrazoxane hydrochloride
Drug ID BADD_D00634
Description An antimitotic agent with immunosuppressive properties. Dexrazoxane, the (+)-enantiomorph of razoxane, provides cardioprotection against anthracycline toxicity. It appears to inhibit formation of a toxic iron-anthracycline complex. [PubChem] The Food and Drug Administration has designated dexrazoxane as an orphan drug for use in the prevention or reduction in the incidence and severity of anthracycline-induced cardiomyopathy.
Indications and Usage For reducing the incidence and severity of cardiomyopathy associated with doxorubicin administration in women with metastatic breast cancer who have received a cumulative doxorubicin hydrochloride dose of 300 mg/m^2 and would benefit from continued doxorubicin therapy. Also approved for the treatment of extravasation from intravenous anthracyclines.
Marketing Status Prescription
ATC Code V03AF02
DrugBank ID DB00380
KEGG ID D07807
MeSH ID D064730
PubChem ID 6918223
TTD Drug ID D07XVN
NDC Product Code 76310-110; 51991-942
Synonyms Dexrazoxane | Razoxane, (S)-Isomer | Cardioxane | Cardioxan | Zinecard | ICRF-187 | ICRF 187 | ICRF187 | NSC-169780 | NSC 169780 | NSC169780 | ADR-529 | ADR 529 | ADR529 | Dexrazoxane Hydrochloride | Hydrochloride, Dexrazoxane | Razoxane, (S)-Isomer, Hydrochloride
Chemical Information
Molecular Formula C11H17ClN4O4
CAS Registry Number 149003-01-0
SMILES CC(CN1CC(=O)NC(=O)C1)N2CC(=O)NC(=O)C2.Cl
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)
Malaise08.01.01.003--
Nausea07.01.07.001--
Neurotoxicity17.02.10.002; 12.03.01.011--Not Available
Neutropenia01.02.03.004--Not Available
Neutrophil count decreased13.01.06.010--
Oedema peripheral14.05.06.011; 08.01.07.007; 02.05.04.007--
Oesophagitis07.08.05.001--
Phlebitis24.05.03.001; 12.02.01.002--
Platelet count decreased13.01.04.001--
Pneumonia11.01.09.003; 22.07.01.003--Not Available
Pyrexia08.05.02.003--
Sepsis11.01.11.003--
Stomatitis07.05.06.005--
Urticaria23.04.02.001; 10.01.06.001--
Vomiting07.01.07.003--
White blood cell count decreased13.01.06.012--
Musculoskeletal disorder15.03.01.004--Not Available
Injection site discomfort12.07.03.019; 08.02.03.018--Not Available
Haemorrhage24.07.01.002--Not Available
Blood bilirubin abnormal13.03.01.016--Not Available
Angiopathy24.03.02.007--Not Available
Blood alkaline phosphatase increased13.04.02.004--
Blood alkaline phosphatase abnormal13.04.02.005--Not Available
Recall phenomenon12.02.06.001; 23.03.07.005--
Cardiac disorder02.01.01.003--Not Available
Connective tissue disorder15.06.01.006--Not Available
Decreased appetite14.03.01.005; 08.01.09.028--
Renal impairment20.01.03.010--Not Available
Bone marrow failure01.03.03.005--
Post procedural infection11.01.08.019; 12.02.05.010--Not Available
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