Clinical effect not specified
Source: DDInter
Antidote · Antidote; Cardioprotective Agent; Extravasation Treatment
Also known as ZINECARD, CARDIOXANE, SAVENE
Dexrazoxane is an iron chelator. Anthracyclines can form semiquinone radical intermediates that react with O2 to produce superoxide anion radicals, which generate hydrogen peroxide and hydroxyl radicals, attacking DNA. The production of free radicals is significantly stimulated by the interaction of doxorubicin with iron. Dexrazoxane chelates iron, thereby protecting against cardiac toxicity and reducing free radical formation.
Clinical effect not specified
Source: DDInter
Clinical effect not specified
Source: DDInter
Clinical effect not specified
Source: DDInter
Clinical effect not specified
Source: DDInter
Clinical effect not specified
Source: DDInter
Clinical effect not specified
Source: DDInter
Reduces the incidence and severity of doxorubicin-induced cardiotoxicity. However, it may also reduce the antitumor efficacy of doxorubicin in some settings.
Dexrazoxane is specifically used to mitigate doxorubicin cardiotoxicity in patients receiving high cumulative doses or those with pre-existing cardiac risk factors. Its use should be carefully weighed against potential impact on antitumor efficacy, especially in the adjuvant setting.
Source: DDInter
5 additional low-confidence interactions hidden — those rows lack a documented mechanism or management plan in our sources.
Continue into a citation-backed clinical answer with the drug context already attached.
Sources: KD Tripathi 7e, Katzung, BNF, Harriet Lane·Verified: 2026-05-10 · House clinical team