ATC code: N06AX25
Pharmacotherapeutic group: Other antidepressants, St. John's wort
Dry extract of St. John's wort inhibits synaptosomal reuptake of the neurotransmitters noradrenaline, serotonin and dopamine. Subchronic administration produces down-regulation of beta-adrenergic receptors; this alters the behaviour of laboratory animals in certain antidepressant models (e.g. the forced swim test) in a manner comparable to synthetic antidepressants.
The activity is attributed to naphthodianthrones such as hypericin and pseudohypericin, phloroglucinol derivatives such as hyperforin, and flavonoids.
Clinical efficacy and safety
In controlled, double-blind and open-label trials versus placebo, symptoms of psychovegetative disorder, mood lability, low mood, nervous restlessness and anxiety showed significant improvement compared with placebo. Compared with various synthetic antidepressants such as amitriptyline, imipramine or maprotiline, as well as benzodiazepines such as bromazepam, St. John's wort extract demonstrated comparable efficacy with a substantially lower incidence of adverse reactions.
⚠️ Warnings
Intense UV exposure should be avoided during treatment.
As sufficient data are not available, the product is not recommended for use in children and adolescents under 18 years of age.
Excipients with known effect:
Each hard capsule contains 17.8 mg of lactose. Patients with rare hereditary problems of galactose intolerance, total lactase deficiency or glucose-galactose malabsorption should not take this medicine.
This medicinal product contains less than 1 mmol sodium (23 mg) per capsule, that is to say essentially "sodium-free".