Drug-induced nonautoimmune hemolytic anemia
| Drug-induced nonautoimmune hemolytic anemia | |
|---|---|
| Synonyms | |
| Pronounce | N/A |
| Specialty | N/A |
| Symptoms | Fatigue (medical), pallor, jaundice, dark urine, tachycardia |
| Complications | Acute kidney injury, heart failure |
| Onset | |
| Duration | |
| Types | N/A |
| Causes | Drug-induced hemolytic anemia |
| Risks | |
| Diagnosis | Complete blood count, reticulocyte count, Coombs test |
| Differential diagnosis | Autoimmune hemolytic anemia, hereditary spherocytosis, G6PD deficiency |
| Prevention | Avoidance of triggering drugs |
| Treatment | Discontinuation of the offending drug, supportive care |
| Medication | |
| Prognosis | Generally good with removal of the offending drug |
| Frequency | Rare |
| Deaths | N/A |
Drug-induced nonautoimmune hemolytic anemia is a form of hemolytic anemia. Non-immune drug induced hemolysis can occur via oxidative mechanisms. This is particularly likely to occur when there is an enzyme deficiency in the antioxidant defense system of the red blood cells. An example is where antimalarial oxidant drugs like primaquine damage red blood cells in Glucose-6-phosphate dehydrogenase deficiency in which the red blood cells are more susceptible to oxidative stress due to reduced NADPH production consequent to the enzyme deficiency
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