citalopram

Brand: Celexa

⚠ BBW Beers Criteria Prototype: fluoxetine
Drug Class: SSRI
Drug Family: antidepressant
Subclass: selective serotonin reuptake inhibitor
Organ Systems: cns

Mechanism of Action

Selectively inhibits the serotonin transporter with high selectivity and minimal effects on norepinephrine or dopamine transporters, CYP enzymes, or muscarinic receptors, making it one of the most selective SSRIs available.

SERT (serotonin transporter)

Indications

  • major depressive disorder
  • off-label: panic disorder
  • off-label: OCD
  • off-label: generalized anxiety disorder

Contraindications

  • concurrent MAOI use
  • concurrent pimozide use
  • congenital long QT syndrome
  • doses >40 mg/day (QT risk)

Adverse Effects

Common

  • nausea
  • somnolence
  • dry mouth
  • increased sweating
  • tremor
  • sexual dysfunction

Serious

  • QT prolongation and torsades de pointes (dose-dependent)
  • serotonin syndrome
  • hyponatremia (SIADH)
  • suicidal ideation

Pharmacokinetics (ADME)

Absorption well absorbed orally; bioavailability ~80%; food has no effect
Distribution protein binding ~80%; Vd ~12 L/kg
Metabolism primarily via CYP2C19 and CYP3A4; mild CYP2D6 inhibitor; active metabolite didesmethylcitalopram
Excretion primarily renal with some fecal; dose reduction required if CrCl <20 mL/min and in hepatic impairment
Half-life 35 hours
Onset 1-4 weeks for antidepressant effect
Peak 4 hours
Duration 24 hours
Protein Binding 80%
Vd 12 L/kg

Drug Interactions

Drug / Agent Mechanism Severity
MAOIs serotonin syndrome contraindicated
pimozide additive QT prolongation contraindicated
omeprazole (CYP2C19 inhibitors) increases citalopram exposure and QT risk moderate
linezolid serotonin syndrome risk major

Nursing Considerations

  1. Maximum dose is 40 mg/day due to QT prolongation risk; 20 mg/day maximum for patients >60 years, those with hepatic impairment, or CYP2C19 poor metabolizers.
  2. Obtain baseline ECG in patients with known cardiac disease, hypokalemia, or hypomagnesemia before initiating; monitor ECG if dose increases.
  3. Monitor serum sodium in elderly patients; citalopram can cause SIADH — suspect if patient develops confusion, headache, or neurological changes.
  4. Educate patients that full antidepressant effect may take 4-6 weeks; partial response at 2 weeks is prognostically favorable.

Clinical Pearls

  • Citalopram has the most dose-dependent QT prolongation of all SSRIs; FDA issued a safety communication in 2011 limiting the maximum dose to 40 mg/day.
  • Its high selectivity and minimal drug interaction profile make it preferred in medically complex patients requiring polypharmacy.

Safety Profile

Pregnancy use-with-caution
Lactation use-with-caution
Renal Adjustment Required
Hepatic Adjustment Required
TDM Not required

Concordance Terms

Cross-referenced clinical concepts — click any term to see all content where it appears.