API
Doxorubicin
Doxorubicin
Antineoplastic agents (anthracycline antibiotic).
Powder For Injection
10mg
Adults: 60–75 mg/m² IV every 21 days or 20–30 mg/m² IV on days 1–3 every 21 days. Pediatrics: 25–30 mg/m² IV weekly. Reduce dose in hepatic impairment (bilirubin 1.2–3 mg/dL: 50% dose; >3 mg/dL: 25% dose). Adjust for prior anthracycline exposure.
Intercalates into DNA, inhibiting topoisomerase IIα, preventing DNA replication and transcription; generates free radicals via redox cycling, inducing DNA and cell membrane damage; disrupts cell cycle progression, leading to apoptosis in rapidly dividing cells.
Breast cancer, ovarian cancer, bladder cancer, lung cancer, thyroid cancer, gastric cancer, Hodgkin lymphoma, non-Hodgkin lymphoma, acute lymphoblastic leukemia, acute myeloid leukemia, multiple myeloma, neuroblastoma, Wilms tumor, soft tissue sarcoma, bone sarcoma.
Myelosuppression, cardiotoxicity (including heart failure), alopecia, mucositis, nausea, vomiting, extravasation tissue necrosis, secondary malignancies, hepatotoxicity, infusion-related reactions, hyperpigmentation of skin and nails.
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