Related Experiment Video
Updated: Aug 24, 2025

Dynamic Light Scattering Analysis for the Determination of the Particle Size of Iron-Carbohydrate Complexes
Published on: July 7, 2023
Decreased Clinical Toxicity and Two-Phase Elimination Kinetics Observed After Intravenous Iron Sucrose Overdose
Jonathan Meadows1, Jakub Furmaga2, Jeffrey Brent3
1Franciscan Health Emergency Medicine, Olympia Fields, Illinois.
Intravenous iron sucrose overdose is less toxic than oral iron overdose, even with high serum iron levels. Supportive care alone may be sufficient, unlike with oral iron poisoning.
Area of Science:
- Emergency Medicine
- Clinical Toxicology
- Pharmacology
Background:
- Management of oral iron overdoses is established, but data on intravenous iron sucrose overdoses are limited.
- Deferoxamine is indicated for oral iron overdose with toxicity signs and serum iron ≥ 500 microg/dL.
- Signs of iron sucrose overdose differ from oral iron overdose symptoms.
Observation:
- A patient with a 1000 mg intravenous iron sucrose overdose (5x prescribed dose) presented well-appearing.
- Serum iron concentration was 1799 microg/dL, significantly above the threshold for deferoxamine.
- The patient had normal bicarbonate and anion gap with an unremarkable physical exam.
Findings:
- Despite high serum iron, the patient showed no severe toxicity and received only supportive care.
- Deferoxamine was not administered due to the lack of clinical toxicity signs.
- Serum iron normalized within 14 hours, and the patient was discharged the next day.
Implications:
- Intravenous iron sucrose overdose appears to have lower toxicity than oral iron salt overdose.
- Supportive care alone may be adequate for intravenous iron sucrose overdose, contrasting with oral overdose management.
- The distinct elimination kinetics of iron sucrose may explain the discrepancy between high serum iron levels and low clinical toxicity.
More Related Videos
Related Concept Videos
Enhanced Elimination of Poison
Antidotes serve a crucial role in counteracting the effects of poison by inhibiting enzymes responsible for producing harmful drug metabolites. In some cases, these toxic metabolites can be neutralized by endogenous cosubstrates, which are maintained at specific concentrations to prevent interaction with cellular macromolecules and subsequent cell death.
Renal excretion is the...
Prevention of Further Absorption of Poison
Nonlinear Pharmacokinetics: Drug Elimination for IV Bolus Injection
Following the administration of a single intravenous (IV) bolus injection, we can determine the concentration of the drug in the plasma at any given time. This calculation is achieved using a specific equation that integrates the values of Vmax and KM.
We can also...
Renal Failure: Dose Adjustments
Reduced renal clearance and elimination rate are common outcomes of renal impairment. These alterations lead to a prolonged elimination half-life and an altered apparent volume of distribution for drugs. As a result, dosage adjustments are typically necessary to maintain optimal drug levels in the body.
However, dosage adjustments...
Phase II Reactions: Miscellaneous Conjugation Reactions
A key example involves the conjugation of cyanide ions, which impair cellular respiration and alter hemoglobin into non-oxygen-carrying cyanmethemoglobin. To neutralize this threat, a sulfur atom from thiosulphate is transferred to the cyanide ion, catalyzed by the enzyme rhodanese, resulting in an inactive compound called thiocyanate. The production of...
Drug Metabolism: Phase II Reactions

