Clinical Overview
Citalopram is a selective serotonin reuptake inhibitor (SSRI) indicated for major depressive disorder. It has high selectivity for the serotonin transporter with minimal effects on other neurotransmitter systems, but requires dose limitations due to QT prolongation risk at higher doses.
Primary Clinical Applications
Citalopram is indicated for major depressive disorder in adults. It was one of the most widely prescribed antidepressants due to its efficacy and tolerability, though dose restrictions implemented in 2011 have limited its use compared to other SSRIs with fewer cardiac concerns.
Mechanism and Pharmacological Profile
Citalopram selectively inhibits serotonin reuptake with high specificity and minimal activity at other receptors. However, it blocks cardiac potassium channels in a dose-dependent manner, leading to QT interval prolongation and FDA-mandated maximum dose restrictions.
Clinical Considerations
The FDA has established maximum dose limits: 40 mg daily for most adults, and 20 mg daily for patients over 60 years, those with hepatic impairment, or CYP2C19 poor metabolizers. These restrictions have made other SSRIs more favorable choices for patients requiring higher doses.
Prescribing Information
Dosing & Administration
Major Depressive Disorder – Adults:
- Initial: 20 mg once daily
- Range: 20-40 mg daily
- Maximum: 40 mg daily (general population)
Dose Restrictions:
- Patients >60 years: Maximum 20 mg daily
- Hepatic impairment: Maximum 20 mg daily
- CYP2C19 poor metabolizers: Maximum 20 mg daily
Administration:
- Take once daily, morning or evening
- With or without food
- Same time each day for consistency
Indications
- Treatment of major depressive disorder in adults
Contraindications
- Hypersensitivity to citalopram
- Use with MAOIs (within 14 days)
- Use with pimozide
- Congenital long QT syndrome
- Use with linezolid or IV methylene blue
Warnings & Precautions
- Boxed Warning: Increased risk of suicidal thoughts and behavior in patients under 25 years
- QT prolongation: Dose-dependent risk – maximum dose restrictions apply
- Serotonin syndrome: Risk with concurrent serotonergic drugs
- Activation of mania: Monitor in patients with bipolar disorder
- Discontinuation syndrome: Taper gradually when stopping
- Hyponatremia: Particularly in elderly patients
Drug Interactions
- MAOIs: Contraindicated – minimum 14-day washout
- Pimozide: Contraindicated – QT prolongation risk
- QT-prolonging drugs: Use caution, monitor ECG
- CYP2C19 inhibitors: May increase citalopram levels
- Anticoagulants: Increased bleeding risk
Adverse Reactions
Common (≥5%):
- Nausea, dry mouth, somnolence, insomnia
- Sweating increased, tremor, diarrhea
- Sexual dysfunction, fatigue
Serious:
- QT prolongation, serotonin syndrome, abnormal bleeding
Special Populations
- Elderly (>60 years): Maximum 20 mg daily due to QT risk
- Hepatic Impairment: Maximum 20 mg daily
- CYP2C19 poor metabolizers: Maximum 20 mg daily
- Pregnancy: Category C – use only if benefits outweigh risks
- Cardiac monitoring: Consider ECG in patients with cardiac risk factors