Desferrioxamine 2g powder for solution for injection vials
Requires a prescription from a doctor or prescriber
Natural product isolated from Streptomyces pilosus.
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Safety monitoring data
Yellow Card reports
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Suspected adverse reactions reported for Desferrioxamine
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Data from the MHRA Yellow Card scheme. A reported reaction does not necessarily mean the medicine caused it. Contains public sector information licensed under the Open Government Licence v3.0.
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4 branded products available
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Desferrioxamine 2g powder for solution for injection vials
Therapeutically similar medicines
Similarity is based on WHO Anatomical Therapeutic Chemical (ATC) classification and on a factual NHS dm+d therapeutic-grouping code prefix. Source data: NHS dm+d via TRUD (OGL v3.0), WHO ATC/DDD Index.
NHS prescribing volume and spending trends
Guidelines from the National Institute for Health and Care Excellence
NICE clinical guidance(2)
Spectra Optia for automatic red blood cell exchange in people with sickle cell disease (HTG405)
Chronic kidney disease: assessment and management (NG203)
Source: National Institute for Health and Care Excellence (NICE). Contains public sector information licensed under the Open Government Licence v3.0.
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Pharmacy links redirect to the retailer's own search and do not represent real-time stock levels. Shortage and safety information sourced from MHRA drug safety updates (gov.uk, Crown Copyright under OGL v3.0).
Codes for healthcare professionals and prescribing systems
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NHS UK identifiers
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SNOMED CT and dm+d codes from NHS TRUD (Technology Reference data Update Distribution), licensed under the Open Government Licence v3.0. BNF code shown is the factual mapping value distributed by NHS Business Services Authority (NHSBSA) in the dm+d supplementary file under OGL v3.0; it is not affiliated with, nor licensed from, the publishers of the British National Formulary. ATC codes from the WHO Collaborating Centre for Drug Statistics Methodology (whocc.no).
Active and completed clinical studies from ClinicalTrials.gov
Source: ClinicalTrials.gov, a database of the U.S. National Library of Medicine (NLM), National Institutes of Health (NIH). Data accessed via ClinicalTrials.gov API v2. Trial information is provided for research purposes and does not constitute medical advice.
Academic studies and reviews for this medicine's active substance
Showing the 50 most relevant studies.
Reviews & meta-analyses: 7 · Randomised trials: 2 · 1964–2024
Showing the 50 most relevant studies, sorted by most relevant.
B. Halliwell
Free radical biology & medicine, 1989
- Deferoxamine
- Free Radicals
Yu Yu, Jacky Wong, David B. Lovejoy, et al.
Clinical Cancer Research, 2006
- Antineoplastic Agents
- Chelating Agents
- Deferoxamine
Lingzhi Kong, Zhi Wu, Huakun Zhao, et al.
ACS Applied Materials & Interfaces, 2018
- Ceramics
- Deferoxamine
- Gene Expression Regulation
Jie Lan, Dongmei Jiang
Journal of Neural Transmission, 1997
- Iron
- Nerve Degeneration
- 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine
Khadeeja Iram, Zulfiqar Ali, Fauzia Aamer, et al.
Pakistan Journal of Health Sciences, 2024
Iron chelation treatments as adjuvant therapy can reduce iron stores to minimize the related morbidity and mortality in patients with thalassemia major. Objective: To compare Deferasirox (DFX) and Desferrioxamine (DFO) in terms of mean serum ferritin levels in patients of β-thalassemia major having Iron overload. Methods: This randomized controlled trial was conducted at the Thalassemia Center of Hematology Department, “The Children's Hospital and The Institute of Child Health”, Multan, Pakistan from January 2023 to September 2023. After randomization, children in DFO group were given DFO in a dose of 50mg/kg, through subcutaneous route by infusion pump five days a week. Children in DFX group were given DFX in a dose of 30mg/kg, orally in tablet form once daily. Baseline serum ferritin levels were measured and the change in mean serum ferritin level for each group was calculated and compared for both groups after 6-months of treatment. Results: In a total of 142 children, 87 (61.3%) children were male. The mean age was 7.08 ± 2.41 years. The mean number of blood transfusions at the time of enrollment were 13.4 ± 4.2. After 6 months of treatment in DFO versus DFX groups, the net change in mean serum ferritin levels from baseline to post-treatment was 947.2 ± 454.0 µg/L for DFO and 1053.5 ± 389.8 µg/L for DFX, with no statistically significant difference between the groups (p=0.1367). Conclusions: Once-daily oral deferasirox has good compliance, acceptable tolerability and appears to have similar efficacy to desferrioxamine in reducing iron burden of transfused patients with beta thalassemia major.
Abstract licence: CC BY 4.0
Rachel Codd, Tomas Richardson‐Sanchez, Thomas J. Telfer, et al.
ACS Chemical Biology, 2017
- Anti-Bacterial Agents
- Biochemistry
- Deferoxamine
Guang-lei Wang, G. Semenza
Blood, 1993
D. R. Crapper McLachlan
The Lancet, 1991
- Alzheimer Disease
- Analysis of Variance
- Chromatography, High Pressure Liquid
John M.C. Gutteridge, Ramsay Richmond, Barry Halliwell
Biochemical Journal, 1979
- Chelating Agents
- Deferoxamine
- Free Radicals
L. Anderson, B. Wonke, E. Prescott, et al.
Lancet, 2002
- Deferiprone
- Deferoxamine
- Echocardiography
Sources: aggregated from Europe PMC (EMBL-EBI), OpenAlex, Crossref, PubMed and other open scholarly databases. Retracted articles are excluded. Study information is provided for research purposes and does not constitute medical advice.
Pharmacology and chemical data from DrugBank
Key facts
Drug status
Approved
Major interactions
None known
Half-life
1 hour
Mechanism
Deferoxamine works in treating iron toxicity by binding trivalent (ferric) iron…
Food interactions
None known
Human targets
3 targets
Data: DrugBank · CC BY-NC 4.0
Pharmacokinetics at a glance
Absorption
Half-life
1 hour
Protein binding
10%
Metabolism
Elimination
Pharmacokinetic data: DrugBank · CC BY-NC 4.0
Known interactions with other medications. Always consult a healthcare professional.
Showing 8 of 8 interactions
Nephrotoxicity, ototoxicity and retinal toxicity have been reported following long-term administration for chronic iron overload.
How the body processes this drug — absorption, distribution, metabolism, and elimination
Proteins and enzymes this drug interacts with in the body
PMID:25122912
Involved in cell mobility and transcription regulation through protein-protein interactions. Can promote transcription activation through binding to APBB1-KAT5 and inhibits Notch signaling through interaction with Numb.
Couples to apoptosis-inducing pathways such as those mediated by G(o) and JIP. Inhibits G(o) alpha ATPase activity (By similarity). Acts as a kinesin I membrane receptor, mediating the axonal transport of beta-secretase and presenilin 1 (By similarity).
By acting as a kinesin I membrane receptor, plays a role in axonal anterograde transport of cargo towards synapses in axons .
PMID:17062754 PMID:23011729
Involved in copper homeostasis/oxidative stress through copper ion reduction. In vitro, copper-metallated APP induces neuronal death directly or is potentiated through Cu(2+)-mediated low-density lipoprotein oxidation. Can regulate neurite outgrowth through binding to components of the extracellular matrix such as heparin and collagen I and IV.
The splice isoforms that contain the BPTI domain possess protease inhibitor activity. Induces a AGER-dependent pathway that involves activation of p38 MAPK, resulting in internalization of amyloid-beta peptide and leading to mitochondrial dysfunction in cultured cortical neurons. Provides Cu(2+) ions for GPC1 which are required for release of nitric oxide (NO) and subsequent degradation of the heparan sulfate chains on GPC1
Enzymes involved in drug metabolism — important for understanding drug interactions
ATC V03AC01
Chemical identifiers
CAS, UNII, InChI Key and database cross-references
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Chemical identifiers
CAS, UNII, InChI Key and database cross-references
Linked compound data from DrugBank Open Data (CC BY-NC 4.0)
Deferoxamine
Matched from: Desferrioxamine
Additional database identifiers
Drugs Product Database (DPD)
2446
ChemSpider
2867
BindingDB
47715
PDB
KTY
ZINC
ZINC000003830635
HUGO Gene Nomenclature Committee (HGNC)
HGNC:620
GenAtlas
APP
GeneCards
APP
GenBank Gene Database
X06989
UniProt Accession
A4_HUMAN
HUGO Gene Nomenclature Committee (HGNC)
HGNC:12805
GenAtlas
XDH
GeneCards
XDH
GenBank Gene Database
D11456
GenBank Protein Database
10336525
Guide to Pharmacology
2646
UniProt Accession
XDH_HUMAN
DrugBank citations
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Structured knowledge from the free knowledge base
ATC classifications (Wikidata)
Linked open data from Wikidata (Q419618), a free and open knowledge base operated by the Wikimedia Foundation. Data is available under the Creative Commons CC0 1.0 Public Domain Dedication. WHO INN from the World Health Organization.