Herbs & Botanicals

Evidence overview

Ashwagandha

Ashwagandha (Withania somnifera) is one of the most-researched adaptogenic herbs in modern supplement science, with a clinical literature concentrated heavily on anxiety, stress, and sleep, plus secondary research streams in strength, testosterone, and cognitive function. It carries a provisional recommendation for anxiety in the World Federation of Societies of Biological Psychiatry / Canadian Network for Mood and Anxiety Treatments clinician guidelines, one of several herbal products graded there.

Or browse all supplements

It carries a provisional recommendation for anxiety in the World Federation of Societies of Biological Psychiatry / Canadian Network for Mood and Anxiety Treatments clinician guidelines, one of several herbal products graded there.

Most studied for

Cognitive performance

277 studies

PubMed coverage

835 studies

Across all indexed goals

Safety profile

Moderate

Based on 137 safety studies

Mechanism class

Adaptogenic herb from the nightshade family used in Ayurvedic medicine for centuries. Constituents include...

Study coverage

Study coverage by goal

PubMed counts for Ashwagandha grouped by the goal each study targets.

Ashwagandha835 studies on PubMed
Your report covers:Cognitive Performance & Neuroprotection · Mood, Stress & Neurological Well-being · Dosage & Protocol · Safety (137 studies)

Evidence

What the evidence covers

What's been studied. Conclusions live in the full report.

Ashwagandha (Withania somnifera) is one of the most-researched adaptogenic herbs in the supplement literature, with clinical research concentrated on anxiety and stress (the dominant use), sleep quality, athletic performance and strength, testosterone and male reproductive health, and cognitive function. The herb has been used in Ayurvedic medicine for centuries; modern supplement research uses standardized root or root-and-leaf extracts, most commonly KSM-66 and Sensoril (two branded extracts that dominate the trial literature). Active constituents include withanolides, steroidal lactones whose mechanisms are still being characterized in modern pharmacology.

The outcome dimensions covered most heavily are anxiety and stress (the supplement's primary established use, anchored by a 2022 WFSBP/CANMAT clinician-guidelines document), sleep quality (a rapidly growing literature with multiple recent meta-analyses), strength and athletic performance, testosterone and male fertility markers (smaller and more contested), and general cognitive function. Cortisol modulation is a consistently-measured biomarker across many of these outcomes; the supplement has well-documented short-term effects on serum cortisol, which is the mechanistic basis often cited across indications.

Demographically, the literature concentrates on healthy adults under stress (the dominant trial population), with substantial subsamples in clinical anxiety, athletic populations, and males with fertility concerns. Specific extract differences (KSM-66 vs. Sensoril vs. generic standardized) is a methodologically important question that the field is still working through; head-to-head comparisons are thinner than the market implies. Trial duration is typically 6-12 weeks, which is shorter than would be ideal for establishing long-term safety and durability of effects.

What the studies found for the goal you choose is in our full report.

Safety

Safety summary

Common adverse events, drug interactions, and special populations.

Ashwagandha is generally well-tolerated in short-to-medium-term trials (typically up to 12 weeks). The most-common adverse effects are mild gastrointestinal discomfort, drowsiness, and headache. Concerns have been raised in the recent literature about possible liver-injury cases, with rare severe cases reported mainly in people with pre-existing liver disease; several national regulators (including in Germany and Australia) have issued cautionary statements about ashwagandha-associated hepatotoxicity, though the absolute risk appears low and the mechanism remains unclear. Drug interactions include theoretical additivity with sedatives and a possible reduced effect of immunosuppressants, plus possible interactions with thyroid hormone, diabetes and blood-pressure medicines, and the herb is generally contraindicated in pregnancy (possible abortifacient effects reported in traditional and preclinical sources). People with autoimmune or thyroid conditions should consult a clinician before use; NIH advises avoiding it during pregnancy and breastfeeding.

This summary is informational and not medical advice. Consult a clinician before starting or changing any supplement, especially if you take prescription medications.

Our full report covers the doses used in studies, drug interactions and contraindications, and what those studies found for the goal you choose.

Foundations

Foundation of the evidence base

A few studies the field anchors on. Not the full picture, just the starting points.

  • Expert-society clinician guidelines (WFSBP/CANMAT Taskforce)World Journal of Biological Psychiatry, 2022

    Expert-society consensus document from the World Federation of Societies of Biological Psychiatry and Canadian Network for Mood and Anxiety Treatments that assesses ashwagandha's efficacy for anxiety disorders. The field's clearest practice-guideline-level positioning of ashwagandha, as a provisional rather than full recommendation.

    View on PubMed
  • Systematic review and meta-analysisPhytotherapy Research, 2022Pooled RCT data across anxiety and stress trials

    Widely-cited systematic review and meta-analysis on ashwagandha's effects in anxiety and stress - the supplement's primary established use. Provides a pooled evidence synthesis published after, and independent of, the WFSBP/CANMAT guideline.

    View on PubMed

Limitations

What this page doesn't answer

Where the public summary stops and the full report begins.

This page summarizes the ashwagandha literature at a general level. It does not address which extract (KSM-66, Sensoril, or generic standardized) is right for your specific goal, what dose has been shown effective in trials relevant to your goal (on Starter, matched to your age and sex), the appropriate duration of use (most evidence is from 6-12 week trials), or how ashwagandha interacts with the medications, supplements, and conditions you have. The recent regulatory caution about hepatotoxicity in some markets adds an additional layer of decision-making that benefits from personalized framing rather than population-level summary.

Label to evidence

More than Ashwagandha on the label?

Photograph the Supplement Facts panel and Veraflux reads every ingredient printed on it, including the ones a proprietary blend lists without doses, then pulls the published research on each. A free account covers 15 ingredients a month, enough for a full label.

Goal-specific evidence

Get the full Ashwagandha report

Your free monthly report adds the things this page doesn't: per-goal evidence breakdown, full citation list, and a safety section covering all adults, opening with a short plain-language summary so you can orient in seconds before drilling in. On Starter, the report is written for your age and sex too.

A free report every month. No credit card. Cancel anytime.

Get notified when new evidence appears

We'll email you when the literature on Ashwagandha materially updates. No account required.

The human-verification check couldn't load, possibly because of a browser extension. You can still submit; if it doesn't go through, try disabling your blocker for this page.