The RR was 1.03 (95% CI 0.84–1.26; 5 studies; 773 patients), indicating a slightly higher risk of discontinuation of study medication in the escitalopram group than in the placebo group, but this difference did not reach statistical significance as the 95% CI included the null value of 1.0.
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Cardiovascular adverse reactions associated with escitalopram in patients with underlying cardiovascular diseases: a systematic review and meta-analysis.
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