Supplement Studies  /  evidence, scored
Evidence File 029 · Ashwagandha · Method v0.14 of 4 claims researched

AshwagandhaWithania somnifera root extract · 4 claims

The cortisol reduction is real. Whether people actually feel less stressed is where the meta-analyses stop agreeing. And one country has banned it.

4Claims scored
8Sources
~600 mgStudied dose
Jul 26Reviewed

Claim 01


Lowers cortisol
5.6/10
Emerging·Replicated · but cortisol is a marker, not a feeling

Multiple meta-analyses report significant cortisol reduction. A 2025 synthesis titled around exactly this point found significant cortisol reduction. A 2024 analysis of 9 RCTs and 558 participants found lowered cortisol alongside perceived stress and anxiety scores.

The consistency across independent syntheses is real. The question the next claim raises is whether it matters.

The working

6Quantity
5Quality
7Consistency
4Directness

(6 × 0.25) + (5 × 0.35) + (7 × 0.25) + (4 × 0.15) = 5.6
Directness scores 4. Serum cortisol is a biomarker several steps removed from what a person buying this actually wants.

Claim 02


Reduces perceived stress
5.2/10
Contested·Meta-analyses disagree on the outcome that matters

The 2025 meta-analysis is explicit in its own title: significant cortisol reduction, no effect on perceived stress. That is a biomarker-outcome dissociation of exactly the kind this format exists to surface.

Other syntheses disagree. A 2024 analysis of 9 RCTs found significant reduction on the Perceived Stress Scale and the Hamilton Anxiety Scale as well as cortisol. A 2025 analysis in BJPsych Open covering 15 studies and 873 patients examined the same question.

A recurring caveat across all of them is extract variability — different trials use materially different preparations, which limits what pooling them can tell you.

The working

6Quantity
5Quality
3Consistency
8Directness

(6 × 0.25) + (5 × 0.35) + (3 × 0.25) + (8 × 0.15) = 5.2
Consistency scores 3. The 2025 synthesis found the biomarker moved and the experience did not; other syntheses found both moved.

Claim 03


Improves sleep quality
6.0/10
Moderate·12 RCTs · 1,002 adults · small effect

A meta-analysis of randomised trials comparing ashwagandha capsules to placebo found small improvements in sleep quantity and quality, particularly in adults treated for more than 8 weeks. A further analysis of 12 randomised trials across 1,002 adults compared specific doses to placebo.

No serious adverse effects were reported in these trials, though reviewers note longer-term safety data are lacking. Reported side effects include diarrhoea, headache, sedation and nausea.

The working

6Quantity
5Quality
6Consistency
8Directness

(6 × 0.25) + (5 × 0.35) + (6 × 0.25) + (8 × 0.15) = 6.0
Better supported than the stress claim and more modestly promoted, which is an unusual combination.

Claim 04


Can cause liver injury
7.3/10
Supported·LiverTox category C · regulatory action taken

LiverTox classifies ashwagandha as a probable cause of clinically apparent liver injury — likelihood score C. A case series drawn from Iceland and the US Drug-Induced Liver Injury Network documented the pattern, and further cases have been assessed for causality using the updated RUCAM instrument.

The injury pattern is typically cholestatic. A published case describes a 22-year-old with no medical history developing severe itching, jaundice and liver injury roughly 30 hours after starting ashwagandha at the manufacturer’s recommended dose, having bought it after seeing a social media advertisement. Reported cases generally resolve after stopping.

Denmark has banned it. The French food safety agency ANSES issued a formal opinion in 2024 on the risks of Withania somnifera preparations in food supplements. This is the single most under-communicated fact about the most-hyped supplement on the market.

The working

6Quantity
7Quality
8Consistency
9Directness

(6 × 0.25) + (7 × 0.35) + (8 × 0.25) + (9 × 0.15) = 7.3
Scored as support for the harm claim. Case series with formal causality assessment, an international registry classification, and two national regulators acting on it.

Dosage as studied


Most-studied regimen
~600 mg per day, extract

Trials vary widely by extract type, which the reviewers identify as a core limitation. Sleep benefits appeared mainly after 8 weeks.

Trial doses
Highly variable. Reviewers identify variability in the extracts studied as a major limitation on interpreting the whole literature.
Duration
Sleep improvements appeared particularly in adults treated for more than 8 weeks.
Regulatory status
Denmark has banned it. The French agency ANSES published a formal opinion in 2024 on risks of Withania somnifera preparations in food supplements.
Liver risk
LiverTox classifies ashwagandha as a probable cause of clinically apparent liver injury — likelihood score C.