Adverse Drug Reaction Classification System

Pharmaceutical Information
Drug Name Dexrazoxane
Drug ID BADD_D00633
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 D03730
MeSH ID D064730
PubChem ID 71384
TTD Drug ID D07XVN
NDC Product Code 67457-208; 33656-0001; 0143-9248; 45562-1119; 54893-0097; 67457-207; 50384-0200; 0143-9247
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 C11H16N4O4
CAS Registry Number 24584-09-6
SMILES CC(CN1CC(=O)NC(=O)C1)N2CC(=O)NC(=O)C2
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)
Pneumonia22.07.01.003; 11.01.09.003--Not Available
Pruritus23.03.12.001--
Pyrexia08.05.02.003--
Sensory loss17.02.07.007--Not Available
Sepsis11.01.11.003--
Shock24.06.02.002--Not Available
Skin disorder23.03.03.007--Not Available
Somnolence19.02.05.003; 17.02.04.006--
Stomatitis07.05.06.005--
Syncope17.02.04.008; 24.06.02.012; 02.01.02.008--
Thrombocytopenia01.08.01.002--Not Available
Thrombophlebitis superficial24.01.02.002--
Tremor17.01.06.002--
Urticaria23.04.02.001; 10.01.06.001--
Vaginal haemorrhage24.07.03.005; 21.08.01.001--
Vomiting07.01.07.003--
Weight decreased13.15.01.005--
White blood cell count decreased13.01.06.012--
Cardiotoxicity12.03.01.007; 02.01.01.002--Not Available
Lymphatic disorder01.09.01.003--Not Available
Musculoskeletal discomfort15.03.04.001--Not Available
Injection site swelling12.07.03.018; 08.02.03.017--Not Available
Infusion site pain08.02.05.014; 12.07.05.002--Not Available
Wound complication12.01.08.010--
Haemorrhage24.07.01.002--Not Available
Blood bilirubin abnormal13.03.01.016--Not Available
Angiopathy24.03.02.007--Not Available
Neutropenic infection11.01.08.024; 01.02.03.009--Not Available
Blood alkaline phosphatase increased13.04.02.004--
Recall phenomenon23.03.07.005; 12.02.06.001--
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