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Marketing Status approved; withdrawn
ATC Code V03AF02
DrugBank ID DB00380
KEGG ID D03730
MeSH ID D064730
PubChem ID 71384
TTD Drug ID D07XVN
NDC Product Code 0143-9247; 55150-434; 55150-437; 54893-0097; 0143-9248; 33656-0001; 45562-1119; 50384-0200; 59651-735
UNII 048L81261F
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
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)
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--
Syncope02.11.04.015; 24.06.02.012; 17.02.04.008--
Thrombocytopenia01.08.01.002--Not Available
Tremor17.01.06.002--
Urticaria23.04.02.001; 10.01.06.001--
Vaginal haemorrhage21.08.01.001; 24.07.03.005--
Vomiting07.01.07.003--
Weight decreased13.15.01.005--
White blood cell count decreased13.01.06.012--
Cardiotoxicity02.11.01.009; 12.03.01.007--Not Available
Lymphatic disorder01.09.01.003--Not Available
Musculoskeletal discomfort15.03.04.001--Not Available
Injection site swelling08.02.03.017; 12.07.03.018--Not Available
Infusion site pain08.02.05.014; 12.07.05.002--Not Available
Wound complication23.03.11.044; 12.01.08.010--
Haemorrhage24.07.01.002--Not Available
Blood bilirubin abnormal13.03.04.016--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--
Breast disorder21.05.04.004--Not Available
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