Laboratory Considerations for Prozac (Fluoxetine) Overdose
In a Prozac (fluoxetine) overdose, comprehensive laboratory testing should include complete blood count, comprehensive metabolic panel, ECG, and drug levels, with special attention to cardiac monitoring due to potential QT prolongation and arrhythmias. 1
Initial Laboratory Assessment
Essential Laboratory Tests
Complete Blood Count (CBC)
- To assess for potential hematologic abnormalities
Comprehensive Metabolic Panel (CMP)
- Liver function tests (AST, ALT, bilirubin)
- Renal function (BUN, creatinine)
- Electrolytes (particularly sodium, potassium)
- Glucose levels
Electrocardiogram (ECG)
- Critical for detecting QT interval prolongation
- Monitoring for ventricular tachycardia, including torsades de pointes
- Assessment of other cardiac abnormalities 1
Fluoxetine and Norfluoxetine Levels
- When available, to confirm ingestion and assess severity
- Therapeutic range: 90-300 ng/mL (fluoxetine) and 72-216 ng/mL (norfluoxetine) 2
Additional Tests to Consider
Arterial Blood Gas (ABG)
- If respiratory depression is present or suspected
Toxicology Screen
- To identify co-ingested substances, particularly:
- Tricyclic antidepressants
- Benzodiazepines
- Alcohol
- Other serotonergic medications 1
- To identify co-ingested substances, particularly:
Monitoring Parameters
Cardiac Monitoring
- Continuous ECG monitoring for at least 6 hours post-ingestion
- Vital signs including blood pressure and heart rate
- QT interval assessment at regular intervals 1
Neurological Assessment
- Glasgow Coma Scale (GCS) for quantitative consciousness evaluation
- Monitoring for seizure activity
- Assessment for serotonin syndrome (neuromuscular abnormalities, autonomic hyperactivity, altered mental status) 1
Special Considerations
Co-ingestion Scenarios
- Tricyclic Antidepressants (TCAs): Additional cardiac monitoring and sodium bicarbonate may be needed 3
- Benzodiazepines: Increased risk of respiratory depression; avoid flumazenil 2
- Other Serotonergic Medications: Increased risk of serotonin syndrome 2
High-Risk Patients
- Elderly patients: More susceptible to adverse effects; may require lower thresholds for intervention
- Patients with cardiac disease: Higher risk of arrhythmias
- Patients with hepatic impairment: Impaired drug metabolism 1
Clinical Correlation
Laboratory findings should be interpreted in the context of clinical presentation. Common symptoms of fluoxetine overdose include:
- Tachycardia (24-30% of cases)
- Drowsiness/somnolence (20-30% of cases)
- Tremor (7-8% of cases)
- Nausea/vomiting (6-8% of cases) 4, 5
More severe manifestations may include seizures, coma, and cardiac arrhythmias 1.
Timing of Laboratory Tests
- Initial assessment: Immediately upon presentation
- Follow-up testing: 4-6 hours after initial assessment
- Extended monitoring: For symptomatic patients or those with abnormal initial results 1
Common Pitfalls to Avoid
- Failing to obtain an ECG - Even in seemingly mild cases, cardiac abnormalities can develop
- Overlooking co-ingestions - Particularly important with TCAs, which can significantly worsen prognosis
- Premature discharge - Patients should be observed for at least 6 hours, even if initially asymptomatic
- Administering flumazenil - Contraindicated in mixed overdoses involving TCAs or fluoxetine due to risk of seizures 2, 3
Remember that while fluoxetine overdose is generally considered relatively benign compared to TCAs, fatal outcomes have occurred with doses as low as 520 mg, though causality is not always established 1. Thorough laboratory assessment and monitoring are essential components of proper management.