“Strong” = several concordant meta-analyses or systematic reviews. “Moderate” = one synthesis, or several controlled trials. “Limited” = early trials only. The rating is about the quality of the studies, not about how useful the supplement is.
Lavender essential oil in capsules, studied in the form of a specific preparation, Silexan. In anxious adults, 80 to 160 mg per day reduce anxiety better than placebo, and sleep improves with it, with no measured sedation or dependence.
No trial in this file finds more adverse effects than with placebo, and a network meta-analysis of 100 trials on anxiolytics even finds fewer. No measured sedation: driving is not impaired, up to 320 mg in a single dose and at 80 mg per day in repeated doses, and in recreational drug users, no abuse potential up to 640 mg in a single dose. No measured interaction with the main enzymes that eliminate drugs (cytochromes P450) in 16 volunteers, nor with the combined contraceptive pill (ethinylestradiol and levonorgestrel) in 24 women. If you are undergoing treatment for anxiety or depression, talk to your doctor: the trials compare Silexan to these treatments, none test switching from one to the other. The limitations: all studies involve anxious or depressed individuals, and only the Silexan preparation. For lavender oil inhalation or massage, the 2019 meta-analysis rates the quality of the studies as low. And 80 mg per day, the most tested dose, would be the lower limit of effectiveness.
80 mg per day of Silexan (lavender essential oil in capsules) in most trials; 160 mg per day performed better on all criteria in an analysis of 925 adults.
In a double-blind trial, Silexan performed as well as lorazepam, a benzodiazepine, against generalized anxiety; and in another, stopped overnight, it caused no withdrawal symptoms.
This network meta-analysis, including 100 trials and 28,637 participants, compared the efficacy and acceptability of various anxiolytics. Silexan, the only herbal medicinal product included, proved very effective in reducing anxiety and showed an acceptability comparable to that of placebo. It was also one of the few treatments to result in fewer adverse effects than placebo, offering a well-tolerated treatment option.
Müller TJ, Künzi A, Heitlinger E, Krämer B, von Känel R, Hättenschwiler J, Hilpert M, Imboden C, Holsboer-Trachsler E, Hatzinger M, Kasper S, Bandelow B, Seifritz E. — European archives of psychiatry and clinical neuroscience (2026) — View the source study
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