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Fluoxetine

Original SSRI (1987).

Aliases (2)
Prozac · Sarafem
TYPICAL DOSE
10-20mg AM x 1-2 weeks → 20mg AM target
Daily
ROUTE
CYCLE
STORAGE

Overview

What is Fluoxetine?

Fluoxetine (Prozac) is the prototype SSRI, FDA-approved in 1987 for major depression. Indications now include OCD, bulimia, panic disorder, and PMDD. Long half-life (active metabolite norfluoxetine ~7-15 days).

Key Benefits

Effective for depression, OCD, bulimia, PMDD, and panic disorder. Long half-life buffers missed doses and reduces discontinuation syndrome. Safe in overdose vs older antidepressants.

Mechanism of Action

Selectively inhibits the serotonin transporter (SERT), increasing synaptic serotonin. Mild 5-HT2C antagonism contributes to slight noradrenergic and dopaminergic disinhibition. Active metabolite extends pharmacology.

Pharmacokinetics

·
PeakHalf-life
Approximate curve — visual aid only, not data-precise PK

What to Expect

  • Week 1
    Tolerability and dose-response.
  • Week 2-4
    Early effect window.
  • Week 4-8
    Peak benefit assessment.
  • Week 8+
    Cycle decision point.

Side Effects & Safety

  • Common (>10%): Nausea, headache, insomnia, sexual dysfunction (40-70%), anxiety/jitteriness early.
  • Less common (1-10%): Weight loss early, weight gain long-term, tremor, sweating, anorgasmia.
  • Rare-serious (<1%): Serotonin syndrome, hyponatremia, suicidal ideation <25 yo (FDA black box), QT prolongation at high doses.
  • Specific watch periods: First 4 weeks for activation/suicidal ideation; long half-life means drug interactions persist 5+ weeks after stopping.

References

PMID 29477251

pubmed.ncbi.nlm.nih.gov · 2018

Cipriani 2018 network MA.

View Study

PMID 18316756

pubmed.ncbi.nlm.nih.gov

SSRI sexual dysfunction.

View Study

PMID 19996044

pubmed.ncbi.nlm.nih.gov

Fluoxetine + tamoxifen breast cancer outcomes.

View Study

PMID 15327508

pubmed.ncbi.nlm.nih.gov

Pediatric MDD efficacy (TADS trial).

View Study

PMID 1540999

pubmed.ncbi.nlm.nih.gov

Bulimia 60mg pivotal trial.

View Study
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