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deferoxamine.md

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Deferoxamine

DesFERAL inj 500mg

臨採
TAH Drug Code IDES
Indications Transfusional hemosiderosis especially in thalassemia major; idiopathic hemochromatosis; porphyria cutanea tarda. Acute Fe poisoning. Chronic Al overload with Al-related disease &/or encephalopathy. Test for Fe & Al overload.
Dosing If the patient is normotensive, Desferal is usually given in a single IM dose: 2 g for an adult and 1 g for a child. If the patient is hypotensive, the IV route is recommended. The maximum rate for administration IV is 15 mg/kg/hr and is reduced after 4-6 hrs so that the total IV dose in general does not exceed 80 mg/kg/24 hrs. In an adult patient with severe iron poisoning even infusion of 37.1 g Desferal over 52 hrs has been tolerated without apparent unwanted effects. Therapy should be continued until the serum iron levels are less than the total iron-binding capacity.
Hepatic Impairment Dose adjustment not necessary
Renal Impairment Dose adjustment not necessary
Contraindications Known hypersensitivity to the active substance, except where desensitisation proves possible.
Adverse Effects Rarely, allergic skin reactions, anaphylactic reactions; local irritation at inj site; audiovisual disturbances, lens opacities; GI disturbances; leg cramps; renal or hepatic impairment; reddish brown urine discoloration; thrombocytopenia; CV & neurological disturbances.
Pregnancy Compatible
Lactation No (Limited) Human Data - Probably Compatible
More Info UpToDate