Clinical Overview
Escitalopram is a selective serotonin reuptake inhibitor (SSRI) indicated for major depressive disorder and generalized anxiety disorder. It is the S-enantiomer of citalopram and demonstrates high selectivity for the serotonin transporter with minimal effects on other neurotransmitter systems.
Primary Clinical Applications
Escitalopram is effective for major depressive disorder in adults and adolescents (12+ years) and generalized anxiety disorder in adults. It is often considered first-line treatment due to its favorable efficacy and tolerability profile, with lower drug interaction potential compared to many other antidepressants.
Mechanism and Clinical Benefits
Escitalopram selectively inhibits the serotonin transporter (SERT) with high affinity and selectivity. It has minimal affinity for other receptors, resulting in fewer side effects. The medication demonstrates linear pharmacokinetics and reaches steady-state levels within one week of dosing.
Clinical Advantages
Escitalopram has a favorable side effect profile with relatively low rates of sexual dysfunction, weight gain, and drug interactions compared to other antidepressants. It can be taken with or without food and has predictable dosing across most patient populations.
Prescribing Information
Dosing & Administration
Major Depressive Disorder – Adults:
- Initial: 10 mg once daily
- Range: 10-20 mg once daily
- Maximum: 20 mg once daily
Major Depressive Disorder – Adolescents (12-17 years):
- Initial: 10 mg once daily
- Range: 10-20 mg once daily
- Maximum: 20 mg once daily
Generalized Anxiety Disorder – Adults:
- Initial: 10 mg once daily
- Range: 10-20 mg once daily
- Maximum: 20 mg once daily
Elderly (≥65 years):
- Recommended dose: 10 mg once daily
Administration:
- Take once daily, morning or evening
- With or without food
- Same time each day for consistency
Indications
- Major depressive disorder (adults and adolescents ≥12 years)
- Generalized anxiety disorder (adults)
Contraindications
- Hypersensitivity to escitalopram or citalopram
- Use with MAOIs (within 14 days)
- Use with pimozide
- Use with linezolid or IV methylene blue
Warnings & Precautions
- Boxed Warning: Increased risk of suicidal thoughts and behavior in patients under 25 years
- Serotonin syndrome: Risk with concurrent serotonergic drugs
- QT prolongation: Dose-dependent risk, monitor in predisposed patients
- 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
- Serotonergic drugs: Increased serotonin syndrome risk
- Anticoagulants: Increased bleeding risk
- CYP2C19 inhibitors: May increase escitalopram levels
Adverse Reactions
Common (≥5%):
- Nausea, insomnia, ejaculation disorder, somnolence
- Sweating increased, fatigue, decreased appetite
Less Common:
- Sexual dysfunction, weight changes, dizziness
Special Populations
- Hepatic Impairment: 10 mg once daily (maximum dose)
- Renal Impairment: No dose adjustment needed for mild-moderate impairment
- Elderly: 10 mg once daily recommended
- Pregnancy: Category C – use only if benefits outweigh risks
- QT Risk: Maximum 20 mg daily due to dose-dependent QT prolongation