Fluoxetine is a selective serotonin reuptake inhibitor (SSRI) widely prescribed for the treatment of depression, anxiety, and related conditions. It increases serotonin availability in the synaptic cleft by blocking its reabsorption into neurons, thereby improving communication between nerve cells. Compared to earlier antidepressants (tricyclics, MAOIs), fluoxetine is better tolerated and safer in overdose, which contributed to its global adoption. It was the first SSRI to be marketed (launched as Prozac in 1987) and remains one of the most studied and prescribed antidepressants worldwide.
Fluoxetine is distinguished by its long half-life (2–4 days for the parent drug, up to 16 days for its active metabolite norfluoxetine). This results in a smoother effect, less withdrawal risk if a dose is missed, and easier tapering, though it also means that side effects or drug interactions can persist longer after stopping. Available as capsules, tablets, liquid formulations, and dispersible preparations, it allows flexible prescribing for adults, adolescents, and sometimes children. Treatment response is gradual, typically requiring 2–6 weeks before mood benefits are noticeable, though anxiety symptoms may improve earlier. As with all SSRIs, full benefit often requires months of therapy and consistent adherence alongside psychological or lifestyle interventions.
Fluoxetine is licensed for a broad range of psychiatric and non-psychiatric conditions:
Typical adult starting dose is 20 mg daily, taken in the morning. Dose may be increased in 10–20 mg increments up to 60 mg/day (sometimes 80 mg in OCD). Because of its long half-life, fluoxetine can be dosed every other day in sensitive patients or at the end of therapy tapering. For adolescents, lower starting doses (10 mg) are often used. Dose adjustments take several weeks to show full effect, so clinicians avoid rapid changes. Adherence and regular review are critical.
Most side effects are mild to moderate and improve over time, but some persist. Monitoring is essential, especially early in treatment.
Patients should be educated to report new or worsening mood symptoms, self-harm thoughts, or sudden changes in behaviour. Emergency medical help is required for serotonin syndrome symptoms.
Patients should be encouraged to engage in concurrent non-drug therapies (CBT, exercise, sleep hygiene) for optimal recovery. Regular follow-up appointments are vital to monitor progress and adjust therapy.
Fluoxetine has important interactions because of CYP2D6 inhibition and serotonin effects.
Patients must always inform healthcare providers of all prescription, OTC, and herbal products. Dose adjustments or monitoring may be needed depending on combination therapy.
Overdose: Fluoxetine overdose is rarely fatal alone but can cause agitation, seizures, fast heart rate, nausea, vomiting, drowsiness, or coma. Emergency care is required. Treatment is supportive, sometimes with activated charcoal if recent ingestion. Serotonin syndrome is a risk when combined with other serotonergic agents.
Missed dose: If a dose is missed, take it as soon as remembered. If nearly time for the next dose, skip and resume the usual schedule. Do not double dose. Because of fluoxetine’s long half-life, a missed dose is less likely to cause sudden withdrawal than with shorter-acting SSRIs.
Discontinuation: When stopping therapy, taper gradually under medical advice, though withdrawal symptoms are often mild compared to other SSRIs.
Because fluoxetine therapy is often long-term, encourage patients to use pill organisers or reminders for adherence, but update promptly if dose is adjusted.
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