Parenteral Manual

Deferoxamine mesylate

Disclaimer: Official controlled document is the CHEO online copy. It is the responsibility of user to ensure that any paper copy version is the same as the online version before use.

Alternate Name(s): 
DESFERAL®
Classification: 
Iron Chelating Agent
Original Date: 
August 2005
Revised Date: 
September 2011
Indications: 
  • Facilitate removal of iron in acute iron intoxication
  • Facilitate removal of iron overload associated with hemochromatoses or other chronic iron overload
Reconstitution and Stability: 

VIAL SIZE

STERILE WATER for INJECTION REQUIRED

FINAL CONCENTRATION

500 mg

2 mL

210 mg/mL

2,000 mg

8 mL

210 mg/mL

  • Reconstituted solution stable 7 days at room temperature, do not refrigerate
  • Solutions diluted in NS or D5W stable 16 days at room temperature
  • Protect from light
Compatibility: 

- Solutions Compatible: D5W, NS, ringer's lactate

- Incompatible: do not mix with any other drug

Administration: 

(For approved routes of administration by nursing personnel, refer to Policy for the Administration of Intravenous Medications.)

Chronic Iron Overload: IV or SC infusion

Acute Iron Overload:

SC NO
IM YES
Usual dilution: undiluted
IV Direct

NO

IV Intermittent Infusion YES
Usual dilution: 210 mg/mL
Infusion rate: do not exceed 15 mg/kg/hour
IV Continuous Infusion

YES:

  • When patient in shock or major clinical findings present
  • Adapt rate of infusion to severity of poisoning

Usual dilution: 210 mg/mL
Infusion rate: do not exceed 15 mg/kg/hour

Dosage: 

(For neonatal dosages, refer to Neonatal IV Drug Manual.)

Pediatric
-  Acute iron overdose:     

  • 15 mg/kg/hr IV (Maximum:  6 g/day)
  • 50 mg/kg/dose IM Q6H (Maximum:  6 g/day)
         OR
  • Alternatively: 20 mg/kg IV/IM (Max: 1,000 mg) initially followed by 10 mg/kg IV/IM (Max: 500 mg) at 4-hour intervals for 2 doses; may repeat with 10 mg/kg (Max:500 mg) Q4-12H depending on clinical response (Maximum: 6 g/day)

- Chronic iron overload:  

  • 20-50 mg/kg/day  to be infused subcutaneously over 8-12 hours and repeated daily (Maximum: 2 g/day)
  • 15 mg/kg/hr IV (Maximum: 12 g/day)

 Adult
- Acute iron overdose:     

  • 15 mg/kg/hour IV (Maximum: 6 g/day)
  • 1 g IM stat, then 0.5 g IM Q 4 hours for 2 doses, additional doses of 0.5 g IM Q 4-12 hours up to 6 g/day may be needed depending on the clinical response

- Chronic iron overdose:  

  • 15 mg/kg/hour IV (Maximum: 12 g/day)
  • 0.5-1 g/day IM
  • 1-2 g/day SC over 8-24 hours

- Dose should be titrated based on iron stores and urinary iron excretion.  Begin at lower end of dosing range for younger children.

Potential hazards of parenteral administration: 
  • Pain, pruritis, erythema and induration at site of injection
  • Following too rapid IV injection >15 mg/kg/hr), generalized erythema, urticaria, hypotension, shock and tachycardia
  • Long-term therapy for chronic iron storage disease may cause allergic type reactions (pruritis, rash, tachycardia, fever, anaphylaxis), or other effects (blurred vision, diarrhea, cataracts, abdominal discomfort, leg cramps, or hearing loss, growth retardation)
  • May cause a reddish colour to the urine (not hematuria)
Notes: 
  • For chronic iron overload, SC is the preferred route for most patients; IV may be preferred in patients with massive iron stores and significant organ damage
  • Contraindicated in patients with severe renal failure or anuria
  • Local reactions in SC infusion site may be minimized by diluting the deferoxamine in 5-10 mL SWI and adding 1 mg hydrocortisone to each mL of deferoxamine solution.
References: 

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