პარასკევი, მაისი 1, 2026
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Global Ingredient Risk Index Botanical

Yohimbe

Pausinystalia yohimbe

Also known as: Yohimbine, Corynanthe yohimbe, Quebrachine, Aphrodine, Yohimex

HIGH RISK 7.0/10 How?

Evidence Strength: LIMITED

This ingredient receives a unclassified risk score due to safety concerns identified by health authorities in USA, Canada. Scientific evidence indicates yohimbine acts primarily as an alpha-2 adrenergic receptor antagonist, leading to increased…. Reported adverse effects include nausea and dizziness.

02

Safety Profile

Common Adverse Effects

  • Nausea
  • dizziness
  • headache
  • anxiety
  • increased heart rate

Serious Adverse Effects

  • Hypertension
  • arrhythmias
  • seizures
  • renal failure
  • myocardial infarction

Contraindications

  • Hypertension
  • anxiety disorders
  • cardiovascular disease
  • renal impairment
  • People taking Antidepressants
  • liver disease
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03

Interactions

Drug / Nutrient Interaction Mechanism Warning
Antidepressants increased risk of serotonin syndrome — caution advised. Antihypertensives: potential antagonism — monitor blood pressure. Stimulants: additive effects on heart rate and blood pressure — avoid combination. MAO inhibitors: increased risk of hypertensive crisis — contraindicated. Anticoagulants: potential increased bleeding risk — monitor closely. Monitor
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04

Evidence and Scientific Findings

Overview

Ingredient Overview

Yohimbe is a herbal supplement derived from the bark of the Pausinystalia yohimbe tree, native to Central Africa. It is commonly used in dietary supplements for its purported aphrodisiac effects and to improve sexual performance. Yohimbe is also marketed for weight loss and athletic performance enhancement. Its active compound, yohimbine, is an alkaloid that has been studied for its pharmacological effects on the body.
Classification

Biological and Chemical Classification

Chemical Class
Alkaloid
Biological Class
Plant extract
Natural Source
Pausinystalia yohimbe bark
Scientific Name
Pausinystalia yohimbe
Chemical Formula
C21H26N2O3
CAS Number
146-48-5
Mechanism

Mechanism of Action

Yohimbine acts primarily as an alpha-2 adrenergic receptor antagonist, leading to increased norepinephrine release and enhanced sympathetic nervous system activity. This results in vasodilation and increased blood flow, particularly in the genital area, which may account for its aphrodisiac effects. It also inhibits monoamine oxidase, potentially affecting mood and energy levels. Additionally, yohimbine has been shown to increase lipolysis, contributing to its use in weight loss supplements.
Clinical Evidence

Clinical Evidence of Effectiveness

Indication Evidence Level Summary
General Moderate Clinical evidence on yohimbe's efficacy is mixed, with some studies showing benefits for erectile dysfunction and sexual performance, while others indicate limited effects. Research on its use for weight loss and athletic performance is less robust, with few high-quality trials available. The variability in yohimbe extract composition and yohimbine content complicates the interpretation of results. Overall, the evidence is limited by small sample sizes and methodological weaknesses.
Evidence levels: Strong Moderate Limited Experimental
Pharmacokinetics

Pharmacokinetics

Absorption
Yohimbine is rapidly absorbed after oral administration, with peak plasma concentrations typically reached within 30 to 60 minutes. Its bioavailability is variable, influenced by factors such as food intake and individual metabolism. The half-life of yohimbine is approximately 0.5 to 2 hours.
Distribution
Yohimbine is widely distributed throughout the body, with a volume of distribution indicating extensive tissue uptake. It is known to cross the blood-brain barrier, which may contribute to its central nervous system effects. Yohimbine exhibits moderate protein binding.
Metabolism
Yohimbine is metabolized primarily in the liver by cytochrome P450 enzymes, particularly CYP2D6. The major metabolites include 11-hydroxy-yohimbine and 10-hydroxy-yohimbine, which are excreted in the urine. Genetic polymorphisms in CYP2D6 can affect yohimbine metabolism and clearance.
Excretion
Yohimbine and its metabolites are primarily excreted via the kidneys, with urinary excretion accounting for the majority of elimination. Biliary excretion is minimal. The elimination of yohimbine is rapid, consistent with its short half-life.
Dosage

Recommended Dosage

Condition / Use Typical Dose
Erectile Dysfunction 5-10 mg three times daily. Weight Loss: 10-20 mg per day. Athletic Performance: 0.2 mg/kg body weight.

Dosage ranges are based on clinical studies and commonly used supplement formulations. Individual requirements may vary.

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05

SETI — Scientific Evidence Transparency Index

SETI Score 51/100
Risk Level High risk
Scientific Confidence Low
Evidence Strength Limited
Key Benefit Yohimbe is a herbal supplement derived from the bark of the Pausinystalia yohimbe tree, native to Central Africa.
Key Safety Concern Yohimbe poses significant safety concerns due to its potent pharmacological effects and narrow therapeutic window. It is contraindicated in individuals with cardiovascular conditions, anxiety disorders, and renal impairment. The variability in yohimbine content among supplements raises additional safety issues. Regulatory agencies have issued warnings about its use, particularly in vulnerable populations such as pregnant women and children.
Evidence Reviewed 6 PubMed studies
Scientific Confidence Low
Based on study quality, consistency, and recency

Executive Summary — Ingredient Assessment

SETI Score 51/100
Risk Level High risk
Evidence Strength Limited
Main Benefit Yohimbe is a herbal supplement derived from the bark of the Pausinystalia yohimbe tree, native to Central Africa.
Main Safety Concern Yohimbe poses significant safety concerns due to its potent pharmacological effects and narrow therapeutic window. It is contraindicated in individuals with cardiovascular conditions, anxiety disorders, and renal impairment. The variability in yohimbine content among supplements raises additional safety issues. Regulatory agencies have issued warnings about its use, particularly in vulnerable populations such as pregnant women and children.
Ingredient Yohimbe
Scientific name Pausinystalia yohimbe
Scientific Evidence Overview
  • 6 studies reviewed
  • 0 high-quality studies (meta-analysis or RCT)
  • Main clinical benefit observed: Yohimbe is a herbal supplement derived from the bark of the Pausinystalia yohimbe tree, native to Central Africa.
  • Evidence consistency: High consistency across studies (100%)
Safety Signals
  • Yohimbe poses significant safety concerns due to its potent pharmacological effects and narrow therapeutic window. It is contraindicated in individuals with cardiovascular conditions, anxiety disorders, and renal impairment. The variability in yohimbine content among supplements raises additional safety issues. Regulatory agencies have issued warnings about its use, particularly in vulnerable populations such as pregnant women and children.
Evidence Strength Limited
Regulatory Status
  • USA/FDA — Approved
Final Scientific Assessment

The available scientific evidence for Yohimbe indicates notable safety signals that warrant caution. Use should be considered carefully and monitored, particularly in sensitive populations or alongside other medications.

Ingredient Yohimbe
Evidence reviewed 6 peer-reviewed studies (last 10 years)
Scientific name Pausinystalia yohimbe
51 /100

Total SETI Score

High risk
Evidence quality 6/40
Evidence consistency 20/20
Safety signals 8/20
Study recency 8/10
Evidence transparency 9/10

Evidence Summary

  • 6 studies reviewed
  • 0 high-quality studies (meta-analysis or systematic review)
  • 0 studies identified benefits or no safety concern (GREEN)
  • 6 studies reported limited or advisory safety evidence (YELLOW)

Evidence Policy

Only peer-reviewed scientific literature indexed in PubMed or comparable databases is included in this evaluation. Commercial websites, blogs, and marketing materials are excluded. All references include direct traceable links to source documents.

Last updated: 06 მარ 2026, 12:01

Evidence Distribution

6 Other / unclassified
  1. Observational / other LOW evidence YELLOW
    Multifaced Nature of Yohimbine-A Promising Therapeutic Potential or a Risk? ↗
    Journal Int J Mol Sci
    Year 2024
    Study type Observational / other
    Evidence strength LOW evidence
    Nowacka A et al.. Multifaced Nature of Yohimbine-A Promising Therapeutic Potential or a Risk?. Int J Mol Sci. 2024. PMID:39684567.
  2. Observational / other LOW evidence YELLOW
    Non-targeted chemical analysis of consumer botanical products labeled as blue cohosh (Caulophyllum thalictroides), goldenseal (Hydrastis canadensis), or yohimbe bark (Pausinystalia yohimbe) by… ↗
    Journal Anal Bioanal Chem
    Year 2024
    Study type Observational / other
    Evidence strength LOW evidence
    Quiroz-Delfi GO et al.. Non-targeted chemical analysis of consumer botanical products labeled as blue cohosh (Caulophyllum thalictroides), goldenseal (Hydrastis canadensis), or yohimbe bark (Pausinystalia yohimbe) by NMR and MS.. Anal Bioanal Chem. 2024. PMID:37910202.
  3. Observational / other LOW evidence YELLOW
    Biomedical analysis of New Psychoactive Substances (NPS) of natural origin. ↗
    Journal J Pharm Biomed Anal
    Year 2020
    Study type Observational / other
    Evidence strength LOW evidence
    Lo Faro AF et al.. Biomedical analysis of New Psychoactive Substances (NPS) of natural origin.. J Pharm Biomed Anal. 2020. PMID:31704129.
  4. Observational / other LOW evidence YELLOW
    Alkaloids with Immunosuppressive Activity from the Bark of Pausinystalia yohimbe. ↗
    Journal J Nat Prod
    Year 2018
    Study type Observational / other
    Evidence strength LOW evidence
    Liu Y et al.. Alkaloids with Immunosuppressive Activity from the Bark of Pausinystalia yohimbe.. J Nat Prod. 2018. PMID:30059216.
  5. Observational / other LOW evidence YELLOW
    Chromatographic fingerprinting as a strategy to identify regulated plants in illegal herbal supplements. ↗
    Journal Talanta
    Year 2017
    Study type Observational / other
    Evidence strength LOW evidence
    Custers D et al.. Chromatographic fingerprinting as a strategy to identify regulated plants in illegal herbal supplements.. Talanta. 2017. PMID:28107963.
  6. Observational / other LOW evidence YELLOW
    Yohimbine. ↗
    Year 2012
    Study type Observational / other
    Evidence strength LOW evidence
    Yohimbine.. 2012. PMID:31644013.
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06

Score Transparency

Q × L × D × S × 10 = 7.0 / 10

The GIRI Score is the product of four independently computed evidence components, each normalised to 0–1, then scaled to 0–10. Every component is derived exclusively from peer-reviewed references and regulatory data — no editorial judgement is applied.

Q
Evidence Quantity 0 / 10
0%

0 of 10 approved references (score saturates at 10). More peer-reviewed studies = stronger evidence base.

Method: Q = number of approved references ÷ 10 (capped at 1.0)

L
Evidence Quality 5 / 10
50%

Limited — mostly case reports or animal studies

Method: L = mean study-level weight across approved references. Level 1 (meta-analysis / systematic review) = 1.0; Level 2 (RCT) = 0.8; Level 3 (cohort/case-control) = 0.6; Level 4 (case report) = 0.4; Level 5 (animal / in-vitro) = 0.2.

D
Evidence Direction 5 / 10
Benefit
Risk
50%

Mixed or neutral — roughly equal benefit and risk signals

Method: D = (sum of risk-scored references − sum of benefit-scored references) ÷ total evidence score, then scaled from [−1, 1] to [0, 1]. 0.0 = pure benefit; 0.5 = neutral; 1.0 = pure risk.

S
Safety Signals 8.5 / 10
85%

High volume of active regulatory or adverse-event signals

Method: S = 0.5 (neutral baseline) + sum of active signal severity deltas ÷ 10. Severity deltas: Critical = +2.0, High = +1.5, Moderate = +1.0, Low = +0.5. Capped at 1.0.

0Q × 5L × 5D × 8.5S = 7.0 / 10

Final GIRI Score for Yohimbe. Risk level thresholds: Low 0–3.0 · Moderate 3.0–5.5 · High 5.5–7.5 · Critical 7.5–10.

Full methodology & data sources

The GIRI Score is computed entirely from structured data — no editorial scoring or subjective weighting is applied at any step.

  • References: Only approved references are counted. Each reference is assigned an evidence level (L1–L5) and a direction (risk / neutral / benefit) by the reference manager or AI classifier.
  • Safety Signals: Sourced from regulatory agencies (FDA, EMA, Health Canada, TGA, and others) and pharmacovigilance databases. Only active signals count toward the score.
  • Formula version: GIRI Score v3.7.0 — Q × L × D × S × 10.
  • Limitations: The score reflects published evidence and recorded signals as of the last update date. It is not a clinical risk assessment and should not replace advice from a qualified healthcare professional.
07

Risk Level Classification

HIGH RISK 7.0/10

Based on available regulatory signals and scientific evidence, this ingredient presents a high safety concern. Its use in dietary supplements is associated with documented adverse events.

LOW
0–3.0
MODERATE
3.0–5.5
HIGH
5.5–7.5
CRITICAL
7.5–10
7.0

The score pin shows exactly where this ingredient falls on the fixed risk scale.

What drove the High classification for Yohimbe

GIRI Score 7.0 / 10

A score of 7.0 places this ingredient in the High band. Thresholds: Low 0–3.0 · Moderate 3.0–5.5 · High 5.5–7.5 · Critical 7.5–10.

Evidence Quantity (Q) 0 / 10 refs

0 approved references.

Evidence Quality (L) 50%

Limited — mostly case reports or animal studies (Level 4–5).

Evidence Direction (D) 50% toward risk

Neutral or mixed — benefit and risk signals roughly balanced.

Safety Signals (S) 2 active signals

2 active signals (highest severity: Critical). Each active signal raises S above the neutral baseline of 0.5.

Regulatory Status 1 jurisdiction with restrictions

1 jurisdiction has active restrictions or advisories. Regulatory signals are recorded as Safety Signals and raise the S component.

How are the Low / Moderate / High / Critical thresholds defined?

The four risk levels are fixed score bands. A score is assigned to exactly one level based on where it falls:

LevelScoreMeaning
LOW0.0 – 2.9Sparse or predominantly beneficial evidence. No active safety alerts.
MODERATE3.0 – 5.4Mixed signals — some risk alongside benefit. Caution at high doses or in sensitive groups.
HIGH5.5 – 7.4Multiple studies or regulatory alerts documenting adverse effects. Professional oversight recommended.
CRITICAL7.5 – 10Regulatory restrictions in one or more major jurisdictions. Serious documented harm. Avoid without specialist supervision.

Thresholds are fixed constants (GIRI_Score_Utils::LEVEL_THRESHOLDS). They do not change per ingredient and are never subject to editorial adjustment.

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