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Desferrioxamine

Antidote · Treatment of iron and aluminum overload

Also known as Desferrioxamine mesilate, Deferoxamine Mesilate, Desferal

AntidoteTreatment of iron and aluminum overloadATC V03AC01
CDSCO approvedSchedule HATC V03AC01
EXCRETION
not curated
INTERACTIONS
none in our sources
PREGNANCY
Teratogenic in animal studies. Manufacturer advises use only if potential benefit outweighs risk.
FDA category + note

Mechanism

Deferoxamine is an iron chelating agent that exhibits a remarkably high affinity for ferric iron (Ka = 10^31) and a very low affinity for calcium. It removes iron from hemosiderin and ferritin, and to a lesser extent, from transferrin, but iron in hemoglobin or cytochromes is not removed. It also acts as an effective chelator of copper, mercury, zinc, and lead, promoting their excretion in the urine.

Indications

Chronic iron overload (low iron overload)Chronic iron overload (established overload)Severe iron toxicity (serum iron levels >500 μg/dL)Moderately toxic cases of iron overload (serum iron 350-500 μg/dL)Chronic iron intoxication (e.g., thalassemia)Chelation of aluminum in dialysis patientsAcute iron poisoning

Dosing

Adult
For chronic iron overload: 20–50 mg/kg daily by subcutaneous infusion. For severe iron toxicity (serum iron levels >500 μg/dL): 10–15 mg/kg/hour by constant intravenous infusion. For moderately toxic cases (serum iron 350–500 μg/dL): 50 mg/kg intramuscularly. For chronic iron intoxication (e.g., thalassemia): 0.5–1.0 g/day intramuscularly or 1–2 g/day by continuous subcutaneous administration.…
Max dose
1 g for intramuscular use in moderately toxic cases. 2 g/day for continuous subcutaneous administration in chronic iron intoxication. 2 g per unit of blood for slow intravenous infusion during blood transfusion.

Pharmacokinetics

Bioavailability
Poorly absorbed after oral administration
Metabolism
Metabolized by plasma enzymes, but the pathways have not yet been defined
Excretion
Excreted readily in the urine

Contraindications

  • Aluminium-related encephalopathy (may exacerbate neurological dysfunction)
  • Primary hemochromatosis

Side effects

Common
Arthralgiabone disorderfevergrowth retardationheadachemuscle complaintsnauseaskin reactions
Serious
  • Abdominal pain
  • asthma
  • deafness neurosensory
  • tinnitus
  • vomiting
  • Angioedema
  • blood disorder
  • cataract
  • diarrhoea
  • dizziness
  • encephalopathy
  • eye disorders
  • hypersensitivity
  • hypotension (more common when given too rapidly by intravenous injection)
  • increased risk of infection
  • nerve disorders
  • nervous system disorder
  • paraesthesia
  • respiratory disorders
  • shock
  • tachycardia
  • thrombocytopenia
  • vision disorders
  • Acute kidney injury
  • hypocalcaemia
  • leucopenia
  • renal tubular disorder
  • seizure
  • urine red

Pregnancy & lactation

Pregnancy

Teratogenic in animal studies. Manufacturer advises use only if potential benefit outweighs risk.

Lactation

Manufacturer advises use only if potential benefit outweighs risk—no information available.

Related guidelines

Other Antidote drugs

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Sources: KD Tripathi 7e, BNF·Verified: 2026-05-13 · House clinical team