The following Lexapro side effects have been established in clinical trials:
Autonomic Nervous System Disorders
Central & Peripheral Nervous System Disorders
Gastrointestinal Disorders
Respiratory System Disorders
Urogenital
Side Effects Associated with Discontinuation of Treatment
Among the 715 depressed patients who received Lexapro in placebo-controlled trials, 6% discontinued treatment due to an adverse event, as compared to 2% of 592 patients receiving placebo. In two fixed dose studies, the rate of discontinuation for adverse events in patients receiving 10 mg/day Lexapro was not significantly different from the rate of discontinuation for adverse events in patients receiving placebo. The rate of discontinuation for adverse events in patients assigned to a fixed dose of 20 mg/day Lexapro was 10% which was significantly different from the rate of discontinuation for adverse events in patients receiving 10 mg/day Lexapro (4%) and placebo (3%). Adverse events that were associated with the discontinuation of at least 1% of patients treated with Lexapro, and for which the rate was at least twice the placebo rate, were nausea (2%) and ejaculation disorder (2% of male patients).
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