Ashwagandha
An adaptogenic herb (Withania somnifera) used in Ayurvedic medicine to support stress resilience, energy, and cognitive function.
A flowering plant root used as a natural sleep aid and mild anxiolytic in traditional European herbalism.
Updated February 20, 2026This content is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare provider before starting, stopping, or changing any supplement or medication regimen.
• Sleep quality/insomnia: Research suggests valerian may modestly improve subjective sleep quality and reduce sleep onset latency, particularly after continuous use for 2–4 weeks; effects are small and study results are mixed (moderate evidence from multiple systematic reviews/meta-analyses with heterogeneity). • Anxiety and stress: Some studies show small reductions in mild anxiety or situational stress, but findings are inconsistent and generally weaker than for sleep (emerging-to-moderate evidence from small RCTs and reviews). • Menopause-related symptoms: Limited RCTs suggest valerian may reduce hot-flash frequency/intensity and improve associated sleep disturbance in peri/postmenopausal women (emerging evidence). • Restless legs syndrome (RLS): A small randomized trial reported improvement in RLS symptoms and sleep quality (emerging evidence). • Gastrointestinal spasm/functional discomfort: Traditionally used as an antispasmodic; modern clinical evidence is limited (traditional-to-emerging evidence).
Common (usually mild, often similar to placebo in trials): headache, dizziness/lightheadedness, gastrointestinal upset (nausea, abdominal discomfort), dry mouth, daytime drowsiness or “hangover,” vivid dreams. Dose-related: next-day sedation, impaired attention/reaction time—more likely with higher doses or co-use of other sedatives/alcohol. Less common/rare: pruritus or allergic reactions; paradoxical agitation; rare case reports of liver injury, often involving multi-herb products (causality uncertain). Safety notes: Avoid driving or operating machinery after dosing until individual response is known; sedation risk increases with alcohol, benzodiazepines, opioids, antihistamines, and hypnotics.
Commonly used ranges in studies (not prescriptive; optimal dose varies): • Standardized extract for insomnia: 300–600 mg of valerian root extract (often standardized to ~0.3–0.8% valerenic acids) taken 30–120 minutes before bedtime; some trials used single doses up to ~900 mg. • For anxiety/stress: 120–200 mg extract taken 2–3 times daily in small trials. • Traditional preparations: 2–3 g dried root as tea (steeped 10–15 minutes) or 2–4 mL tincture up to 3 times daily. • Onset: Some benefits appear after single doses, but several trials suggest more consistent effects after daily use for 2–4 weeks.
• Pregnancy and breastfeeding: Insufficient safety data—generally avoided. • Children: Limited data; avoid in very young children and use only with clinician guidance in older children/adolescents. • Liver disease or history of hepatotoxicity: Use cautiously or avoid; consider monitoring if prolonged use. • Concomitant use of CNS depressants (e.g., alcohol, benzodiazepines, opioids, sedative-hypnotics, first-generation antihistamines): Risk of excessive sedation/respiratory depression. • Sleep apnea or respiratory compromise: Use with caution due to sedative effects. • Surgery/anesthesia: Discontinue 1–2 weeks before elective procedures and inform the anesthesiologist, due to potential interactions with anesthetics and withdrawal-like symptoms reported anecdotally with abrupt cessation after heavy use.
| Substance | Type | Severity | Description |
|---|---|---|---|
| Alcohol (ethanol) | synergistic | severe | Additive CNS depression; increases drowsiness, psychomotor impairment, and risk of respiratory depression. |
| Diazepam (benzodiazepine) | synergistic | severe | Valerian’s GABAergic activity may enhance benzodiazepine sedation/anxiolysis, leading to excessive sedation. |
| Zolpidem | synergistic | severe | Additive hypnotic effects and risk of next-day impairment when combined. |
| Oxycodone (opioid) | synergistic | severe | Combined CNS/respiratory depression risk due to overlapping sedative effects. |
| Diphenhydramine | synergistic | moderate | Additive sedation and anticholinergic effects increase cognitive and motor impairment. |
| Propofol (general anesthetic) | synergistic | severe | May potentiate anesthetic/sedative effects; risk of hemodynamic instability or delayed emergence. |
| Kava (Piper methysticum) | synergistic | moderate | Additive sedation; both have been associated (rarely) with liver injury—avoid combining or use only with medical supervision. |
| Melatonin | synergistic | moderate | Combined hypnotic effects may increase next-day drowsiness and psychomotor slowing. |
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Health Disclaimer
This content is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare provider before starting, stopping, or changing any supplement or medication regimen.