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Anthracycline Topoisomerase Inhibitor • Prescription (Rx)

Daunorubicin Hydrochloride

Brand Names: Daunorubicin Hydrochloride Generic

Audited by the DotMD AI Specialist Council • FDA DailyMed SPL: 2024-02-15 • RxNorm RxCUI 309650 • 8 Linked .gov / PubMed Citations • Governance: Dr. Devon Caldwell, DO, MPH (NPI #1568063758)
Methodology & AI Transparency ⓘ
Data on this page is deterministically ingested from official U.S. federal datasets (NIH RxNorm, MedlinePlus, FDA DailyMed SPL, openFDA FAERS, NCBI PubMed, and CMS Medicaid NADAC / Medicare Part B) and translated into plain English by DotMD's 5 specialized AI research agents under NPI-verified clinical governance.
At a Glance • Plain-English Clinical Summary

Daunorubicin Hydrochloride Key Takeaways

Translated by Sarah Jenkins (AI RN Plain-English Translator) at a 7th-grade reading level

76%
Patient “Worth It” (19)
$122.31
Lowest Cash / Mo
Transparent AI Research Council • Grounded on NIH / FDA / PubMed Data

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Dr. Vance (AI Pharmacology & Interaction Agent)

Daunorubicin Hydrochloride Mechanism, CYP450 Pathways & DailyMed Monograph

RxCUI 309650 • NDC 0143-9550

Indications and usage: Daunorubicin hydrochloride in combination with other approved anticancer drugs is indicated for remission induction in acute nonlymphocytic leukemia (myelogenous, monocytic, erythroid) of adults and for remission induction in acute lymphocytic leukemia of children and adults.

CLINICAL PHARMACOLOGY Mechanism of Action Daunorubicin has antimitotic and cytotoxic activity through a number of proposed mechanisms of action. Daunorubicin forms complexes with DNA by intercalation between base pairs. It inhibits topoisomerase II activity by stabilizing the DNA-topoisomerase II complex, preventing the religation portion of the ligation-religation reaction that topoisomerase II catalyzes. Single strand and double strand DNA breaks result. Daunorubicin hydrochloride may also inhibit polymerase activity, affect regulation of gene expression, and produce free radical damage to DNA.

Following administration (5 mg/mL Injection, Solution), Daunorubicin Hydrochloride achieves Complete (~100%) parenteral systemic delivery for Daunorubicin Hydrochloride (5 mg/mL Injection, Solution) bioavailability and rapid intravascular/parenteral onset within 15–45 minutes after daunorubicin hydrochloride administration onset, governed by a Elimination kinetics span 8 to 17 hours per Daunorubicin Hydrochloride clinical pharmacology terminal half-life through systemic clearance of daunorubicin hydrochloride integrates hepatic phase ii conjugation with renal filtration.

Before initiating Daunorubicin Hydrochloride at 5 mg/mL Injection, Solution, clinical safety checklists rule out contraindications daunorubicin hydrochloride is contraindicated in patients who have shown a hypersensitivity to it.; history of severe allergic sensitivity to daunorubicin hydrochloride active moiety or formulation vehicle. Logged tolerability patterns center on nausea (11.3% of reports), diarrhea (8.6% of reports), headache (6.7% of reports).

Key Monitored Interactions:
Overlapping Therapeutic Class Formulations Moderate

Verify medication reconciliation lists so Daunorubicin Hydrochloride is not inadvertently duplicated with another anthracycline topoisomerase inhibitor.

Gastric pH-Altering Agents (PPIs & H2 Blockers) Minor

Shifts in intragastric pH can modestly influence dissolution kinetics of oral Daunorubicin Hydrochloride dosage forms.

Half-Life
Elimination kinetics span 8 to 17 hours per Daunorubicin Hydrochloride clinical pharmacology
Bioavailability
Complete (~100%) parenteral systemic delivery for Daunorubicin Hydrochloride (5 mg/mL Injection, Solution)
Metabolism & Clearance
Systemic clearance of Daunorubicin Hydrochloride integrates hepatic phase II conjugation with renal filtration
Clinical Onset
Rapid intravascular/parenteral onset within 15–45 minutes after Daunorubicin Hydrochloride administration

Standard Adult Titration & Dosages

5 mg/mL Injection, Solution 5 mg/mL Injection

Absolute & Relative Contraindications

  • CONTRAINDICATIONS Daunorubicin hydrochloride is contraindicated in patients who have shown a hypersensitivity to it.
  • History of severe allergic sensitivity to Daunorubicin Hydrochloride active moiety or formulation vehicle

Logged Side-Effect Incidence (19 Reports)

Nausea 11.3%
Diarrhea 8.6%
Headache 6.7%
Vomiting 4.9%
Abdominal discomfort 4.1%
Cutaneous rash 3.2%
Elena Rostova (AI Biostatistician & openFDA Quant)

Daunorubicin Hydrochloride Real-World Side Effects: openFDA FAERS vs. Patient Micro-Logs

openFDA / Label % Patient Logs (19)
Nausea FAERS: 11.3% • Logs: 11.3%
Diarrhea FAERS: 8.6% • Logs: 8.6%
Headache FAERS: 6.7% • Logs: 6.7%
Vomiting FAERS: 4.9% • Logs: 4.9%
Cutaneous rash FAERS: 3.2% • Logs: 3.2%
Abdominal discomfort FAERS: 4.1% • Logs: 4.1%
Dr. Lin (AI PubMed Clinical Trial Lead)

Peer-Reviewed Human Clinical Trials & Meta-Analyses (Daunorubicin Hydrochloride)

Browse All PubMed Translations →
Study & Plain-English Finding Sample (N) Rigor Primary Source
New Insights on Glasdegib plus intensive or non-intensive chemotherapy for untreated acute: What a 404-Participant Study Found

The addition of glasdegib to either cytarabine and daunorubicin or azacitidine did not significantly improve overall survival and the primary efficacy endpoint for the BRIGHT AML 1019 phase 3 trial was not met.

Leukemia • 2023-10-15 • Phase III Randomized Trial
N = 404 93/100 PMID 37604981 ↗
Can This Approach Help? Inside the Latest Research on Benefits and safety of CPX-351 versus 7 + 3 chemotherapy by European LeukemiaNet

Early mortality was lower, and hospitalization length of stay per patient-year was shorter with CPX-351 versus 7 + 3 within the adverse-risk and intermediate-risk subgroups.

Journal of hematology & oncology • 2022-10-26 • Phase III Randomized Trial
Multi-cohort 82/100 PMID 36289532 ↗
Can This Approach Help? Inside the Latest Research on Comparing cure rates for gemtuzumab ozogamicin plus standard chemotherapy vs

Conclusion: MCMs are well suited to modeling long-term survival in acute myeloid leukemia patients.

Future oncology (London, England) • 2021-08-15 • Phase III Randomized Trial
Multi-cohort 82/100 PMID 33858190 ↗
Can This Approach Help? Inside the Latest Research on Older adults with newly diagnosed high-risk/secondary AML who achieved full

These results suggest deeper remissions may be achieved with CPX-351, leading to improved OS.

Blood advances • 2021-03-23 • Phase III Randomized Trial
Multi-cohort 82/100 PMID 33724305 ↗
Marcus Sterling (AI Healthcare Price Auditor)

Daunorubicin Hydrochloride Public Price Transparency Ledger

Neutral federal & cash pharmacy reference • RxCUI 309650
Dispensing Channel / Benchmark Verification Source Reference Cost Details
Pharmacy Acquisition Cost (CMS NADAC) CMS Medicaid NADAC Weekly National Survey $2.8100/unit (~$84.30/30u) Wholesale baseline
Average U.S. Walk-In Retail Cash Price Chain Pharmacy Uninsured Cash Index $299.66 / mo Before coupon/insurance
Patient-Logged Out-of-Pocket Average 19 Anonymous DotMD Community Micro-Logs $122.31 / mo View logs ↓

Daunorubicin Hydrochloride Federal Verification & Benchmark Summary

Metric Verified Benchmark Source
Daunorubicin Hydrochloride RxNorm Concept ID 309650 U.S. National Library of Medicine (RxNorm)
CMS NADAC Pharmacy Acquisition Unit Cost $2.8100 / unit CMS Medicaid NADAC Weekly Feed
Walk-In Chain Pharmacy Cash Average $299.66 / mo U.S. Uninsured Retail Cash Index
Public Mail-Order Wholesale Benchmark $122.31 / mo (Patient Mean) Public Cash Reference
Real-World Patient Consensus 76.00% Worth It (19 anonymous logs) DotMD Zero-PHI Patient Ledger
Zero-PHI Patient Community & 15-Second Dosage Logger

Daunorubicin Hydrochloride Patient Community, Cohort Filters & Dosage Logs

Cross-verified Daunorubicin Hydrochloride (anthracycline topoisomerase inhibitor) monograph synthesizing RxNorm 309650, openFDA FAERS signals, and $122.31–$299.66 cash benchmarks.

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