Most Common Side Effects of Lexapro (Escitalopram)
The most common side effects of Lexapro in adults are nausea (15-18%), insomnia (9-12%), ejaculation disorder (9-14% in males), diarrhea (8%), fatigue (5-8%), and increased sweating, with nausea being the single most frequently reported adverse effect and the most common reason for treatment discontinuation. 1
Gastrointestinal Side Effects
The gastrointestinal system is most commonly affected by escitalopram:
- Nausea occurs in 15% of patients with depression and 18% of patients with generalized anxiety disorder, making it the most prevalent side effect across all indications 1
- Diarrhea affects 8% of patients with depression and 8% with anxiety disorders 1
- Constipation occurs in 3-5% of patients 1
- Dry mouth, indigestion, and abdominal pain each affect 2-3% of patients 1
- The American Academy of Family Physicians notes that escitalopram may be better tolerated than sertraline with lower gastrointestinal side effects 2
Clinical Pearl: Taking escitalopram with food may help reduce nausea, and these gastrointestinal symptoms typically emerge within the first 1-2 weeks of treatment 2
Psychiatric and Sleep-Related Effects
- Insomnia affects 9% of depression patients and 12% of anxiety disorder patients, making it one of the most common reasons for discontinuation 1
- Somnolence (daytime sleepiness) occurs in 6% of depression patients and 13% of anxiety patients 1
- Decreased appetite affects 3% of patients 1
- Vivid dreams and increased sweating are commonly reported 3
Important consideration: The dose-dependent nature of insomnia is notable—14% of patients on 20 mg/day experience insomnia compared to 7% on 10 mg/day 1
Sexual Dysfunction
Sexual side effects are particularly common and often underreported:
- Ejaculation disorder (primarily ejaculatory delay) occurs in 9% of males with depression and 14% of males with generalized anxiety disorder 1
- Decreased libido affects 3-7% of patients 1
- Impotence occurs in 3% of males 1
- Anorgasmia affects 2-6% of females 1
The FDA label explicitly acknowledges that these rates likely underestimate actual incidence due to patient and physician reluctance to discuss sexual problems 1
Neurological Effects
- Dizziness affects 5% of patients 1
- Headache is common (35% in some studies), though often mild 4
- Fatigue occurs in 5-8% of patients 1
- Tremor, nervousness, and bruxism have been reported 3
Dose-Dependent Effects
The 20 mg/day dose shows substantially higher rates of common side effects compared to 10 mg/day:
- Insomnia: 14% vs 7% 1
- Diarrhea: 14% vs 6% 1
- Dry mouth: 9% vs 4% 1
- Somnolence: 9% vs 4% 1
- Increased sweating: 8% vs 3% 1
The overall incidence of adverse events at 20 mg/day (86%) is notably higher than at 10 mg/day (66%) or placebo (61%) 1
Discontinuation Rates
- 6% of depression patients discontinued escitalopram due to adverse events compared to 2% on placebo 1
- 8% of generalized anxiety disorder patients discontinued treatment due to adverse events compared to 4% on placebo 1
- Nausea (2%) and ejaculation disorder (2% of males) were the specific adverse events leading to discontinuation in at least 1% of patients at twice the placebo rate 1
Serious Adverse Events to Monitor
While less common, clinicians must remain vigilant for:
- Increased suicidal thinking and behavior in patients up to age 24 years (pooled absolute risk 1% vs 0.2% with placebo) 3
- Behavioral activation (motor restlessness, insomnia, impulsiveness, aggression), particularly in younger patients early in treatment 3
- QT prolongation, though less commonly reported with escitalopram than citalopram 5, 3
- Serotonin syndrome when combined with other serotonergic medications 2
Comparative Tolerability
- Escitalopram demonstrates better overall tolerability than sertraline, with lower gastrointestinal side effects 2, 3
- Escitalopram has fewer effects on CYP450 enzymes, resulting in lower drug interaction potential compared to other SSRIs 2, 3
- Only nausea occurred in more than 10% of escitalopram-treated patients in pooled analyses 6
Pediatric Considerations
In pediatric patients (ages 6-17), the adverse event profile is generally similar to adults, with additional commonly reported effects including back pain, urinary tract infection, vomiting, and nasal congestion 1