ხუთშაბათი, აპრილი 16, 2026
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Global Ingredient Risk Index Botanical

Green Tea Extract

Camellia sinensis

Also known as: Camellia sinensis extract, GTE, Green Tea Polyphenols, EGCG, Tea Catechins

MODERATE RISK 5.0/10 How?

Evidence Strength: MODERATE

This ingredient receives a unclassified risk score due to safety concerns identified by health authorities in USA. Scientific evidence indicates green Tea Extract exerts its effects primarily through its high content of…. Reported adverse effects include nausea and headache.

02

Safety Profile

Common Adverse Effects

  • Nausea
  • headache
  • dizziness
  • insomnia
  • gastrointestinal upset

Serious Adverse Effects

  • Hepatotoxicity
  • tachycardia
  • hypertension
  • allergic reactions

Contraindications

  • Liver disease
  • cardiovascular disorders
  • anxiety disorders
  • insomnia
  • People taking Warfarin
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03

Interactions

Drug / Nutrient Interaction Mechanism Warning
Warfarin may increase bleeding risk — monitor INR closely. Beta blockers: may reduce efficacy — adjust dose as needed. Antidepressants: may increase stimulant effects — use with caution. Statins: may enhance lipid-lowering effects — monitor lipid levels. Anticoagulants: increased bleeding risk — consider alternative therapies.
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04

Evidence and Scientific Findings

Overview

Ingredient Overview

Green Tea Extract is derived from the leaves of the Camellia sinensis plant. It is commonly used in dietary supplements for its antioxidant properties and potential health benefits, including weight management and cardiovascular health. The extract is rich in polyphenols, particularly catechins, which are believed to contribute to its therapeutic effects.
Classification

Biological and Chemical Classification

Chemical Class
Polyphenol
Biological Class
Antioxidant
Natural Source
Camellia sinensis leaves
Scientific Name
Camellia sinensis
Chemical Formula
C22H18O11
CAS Number
84650-60-2
Mechanism

Mechanism of Action

Green Tea Extract exerts its effects primarily through its high content of catechins, such as epigallocatechin gallate (EGCG). These compounds inhibit oxidative stress by scavenging free radicals and chelating metal ions. EGCG also modulates signaling pathways involved in inflammation and cell proliferation, and may inhibit enzymes like lipoxygenase and cyclooxygenase. Additionally, catechins can influence lipid metabolism and glucose regulation, contributing to their potential weight management benefits.
Clinical Evidence

Clinical Evidence of Effectiveness

Indication Evidence Level Summary
General Moderate Clinical studies on Green Tea Extract have shown mixed results. Some randomized controlled trials suggest benefits in weight management and cardiovascular health, particularly in reducing LDL cholesterol levels. However, the evidence is inconsistent, with some studies showing minimal or no effect. The quality of studies varies, with some lacking rigorous design or having small sample sizes, leading to moderate confidence in the overall conclusions.
Evidence levels: Strong Moderate Limited Experimental
Pharmacokinetics

Pharmacokinetics

Absorption
Green Tea Extract is moderately absorbed when taken orally, with catechins reaching peak plasma concentrations (Cmax) within 1-2 hours. The bioavailability of catechins is relatively low due to extensive first-pass metabolism. The half-life of EGCG is approximately 3-5 hours.
Distribution
Catechins from Green Tea Extract have a moderate volume of distribution and are known to bind to plasma proteins. They are capable of crossing the blood-brain barrier, although the extent of penetration is limited.
Metabolism
Green Tea catechins are metabolized primarily in the liver through phase II conjugation reactions, including glucuronidation and sulfation. Major metabolites include methylated and glucuronidated forms of catechins.
Excretion
Catechins are excreted primarily via the biliary route, with a smaller proportion eliminated in urine. The metabolites are mostly found in feces, indicating significant enterohepatic circulation.
Half-Life
3-5 hours
Dosage

Recommended Dosage

Condition / Use Typical Dose
Weight management 300-600 mg per day. Cardiovascular health: 250-500 mg per day. Antioxidant support: 200-400 mg per day.

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 50/100
Risk Level High risk
Scientific Confidence Low
Evidence Strength Limited
Key Benefit Green Tea Extract is derived from the leaves of the Camellia sinensis plant.
Key Safety Concern Green Tea Extract is generally considered safe for most adults when used at recommended dosages. However, there are reports of liver toxicity, particularly at high doses or with concentrated extracts. Caution is advised in individuals with liver disease, and it is not recommended for use during pregnancy or breastfeeding. Regulatory agencies have issued warnings about potential liver damage, urging consumers to adhere to dosage guidelines.
Evidence Reviewed 10 PubMed studies
Scientific Confidence Low
Based on study quality, consistency, and recency

Executive Summary — Ingredient Assessment

SETI Score 50/100
Risk Level High risk
Evidence Strength Limited
Main Benefit Green Tea Extract is derived from the leaves of the Camellia sinensis plant.
Main Safety Concern Green Tea Extract is generally considered safe for most adults when used at recommended dosages. However, there are reports of liver toxicity, particularly at high doses or with concentrated extracts. Caution is advised in individuals with liver disease, and it is not recommended for use during pregnancy or breastfeeding. Regulatory agencies have issued warnings about potential liver damage, urging consumers to adhere to dosage guidelines.
Ingredient Green Tea Extract
Scientific name Camellia sinensis
Scientific Evidence Overview
  • 10 studies reviewed
  • 0 high-quality studies (meta-analysis or RCT)
  • Main clinical benefit observed: Green Tea Extract is derived from the leaves of the Camellia sinensis plant.
  • Evidence consistency: High consistency across studies (100%)
Safety Signals
  • Green Tea Extract is generally considered safe for most adults when used at recommended dosages. However, there are reports of liver toxicity, particularly at high doses or with concentrated extracts. Caution is advised in individuals with liver disease, and it is not recommended for use during pregnancy or breastfeeding. Regulatory agencies have issued warnings about potential liver damage, urging consumers to adhere to dosage guidelines.
Evidence Strength Limited
Regulatory Status
  • USA/FDA — Approved
Final Scientific Assessment

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

Ingredient Green Tea Extract
Evidence reviewed 10 peer-reviewed studies (last 10 years)
Scientific name Camellia sinensis
50 /100

Total SETI Score

High risk
Evidence quality 10/40
Evidence consistency 20/20
Safety signals 0/20
Study recency 10/10
Evidence transparency 10/10

Evidence Summary

  • 10 studies reviewed
  • 0 high-quality studies (meta-analysis or systematic review)
  • 0 studies identified benefits or no safety concern (GREEN)
  • 10 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

10 Other / unclassified
  1. Observational / other LOW evidence YELLOW
    Tea Quality Alterations Arising from Plant Diseases: Molecular Pathogenesis and Noncoding Ribonucleic Acid-Driven Host-Pathogen Communication. ↗
    Journal J Agric Food Chem
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Naz M et al.. Tea Quality Alterations Arising from Plant Diseases: Molecular Pathogenesis and Noncoding Ribonucleic Acid-Driven Host-Pathogen Communication.. J Agric Food Chem. 2026. PMID:41774081.
  2. Observational / other LOW evidence YELLOW
    Mineral infusion and in-vitro bioaccessibility in Camellia sinensis and herbal tea: influence of matrix and brewing format. ↗
    Journal Front Nutr
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Apaydu0131n H. Mineral infusion and in-vitro bioaccessibility in Camellia sinensis and herbal tea: influence of matrix and brewing format.. Front Nutr. 2026. PMID:41769663.
  3. Observational / other LOW evidence YELLOW
    Unveiling the potential of apigenin and kaempferol against colon cancer: an integrated network pharmacology and docking approach. ↗
    Journal Front Bioinform
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Selvakumar A et al.. Unveiling the potential of apigenin and kaempferol against colon cancer: an integrated network pharmacology and docking approach.. Front Bioinform. 2026. PMID:41768980.
  4. Observational / other LOW evidence YELLOW
    Effects of Photoperiod on Anthocyanin Biosynthesis-Related Gene Expression and Enzymatic Activity in Purple-Leaf Tea Plants (Camellia sinensis). ↗
    Journal Int J Mol Sci
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Li W et al.. Effects of Photoperiod on Anthocyanin Biosynthesis-Related Gene Expression and Enzymatic Activity in Purple-Leaf Tea Plants (Camellia sinensis).. Int J Mol Sci. 2026. PMID:41752001.
  5. Observational / other LOW evidence YELLOW
    Oak (Quercus petraea) Leaf-Based Kombucha: A Sustainable Approach to Fermented Beverages. ↗
    Journal Foods
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Pencak T et al.. Oak (Quercus petraea) Leaf-Based Kombucha: A Sustainable Approach to Fermented Beverages.. Foods. 2026. PMID:41750899.
  6. Observational / other LOW evidence YELLOW
    Intercropping tea plants with different leguminous green manures enhances soil nutrient availability, thereby reshaping the structure and functional potential of soil microbial… ↗
    Journal Front Microbiol
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Liu Q et al.. Intercropping tea plants with different leguminous green manures enhances soil nutrient availability, thereby reshaping the structure and functional potential of soil microbial communities.. Front Microbiol. 2026. PMID:41743141.
  7. Observational / other LOW evidence YELLOW
    Integrative analysis of endogenous phytohormones and transcriptomics reveals mechanism of light-induced callus formation in tea (Camellia sinensis) cuttings. ↗
    Journal BMC Plant Biol
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Gao Y et al.. Integrative analysis of endogenous phytohormones and transcriptomics reveals mechanism of light-induced callus formation in tea (Camellia sinensis) cuttings.. BMC Plant Biol. 2026. PMID:41742034.
  8. Observational / other LOW evidence YELLOW
    Long non-coding RNA Cslnc256 regulates tea plant resistance to anthracnose by suppressing CsmiR395-mediated sulfate metabolism. ↗
    Journal Plant J
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Jiang T et al.. Long non-coding RNA Cslnc256 regulates tea plant resistance to anthracnose by suppressing CsmiR395-mediated sulfate metabolism.. Plant J. 2026. PMID:41723861.
  9. Observational / other LOW evidence YELLOW
    Fluoride detoxification in tea plants depends on aluminium and localization in the epidermis. ↗
    Journal Plant Physiol
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Zhang C et al.. Fluoride detoxification in tea plants depends on aluminium and localization in the epidermis.. Plant Physiol. 2026. PMID:41722032.
  10. Observational / other LOW evidence YELLOW
    Camellia sinensis-synthesized silver nanoparticles and meropenem combination against extensively drug-resistant Klebsiella pneumoniae. ↗
    Journal Sci Rep
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Elmasry EM et al.. Camellia sinensis-synthesized silver nanoparticles and meropenem combination against extensively drug-resistant Klebsiella pneumoniae.. Sci Rep. 2026. PMID:41720838.
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06

Score Transparency

Q × L × D × S × 10 = 5.0 / 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 6.5 / 10
65%

Multiple active safety or regulatory 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 × 6.5S = 5.0 / 10

Final GIRI Score for Green Tea Extract. 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

MODERATE RISK 5.0/10

Based on available regulatory signals and scientific evidence, this ingredient presents a moderate safety concern. Caution is advised, particularly at high doses or in sensitive populations.

LOW
0–3.0
MODERATE
3.0–5.5
HIGH
5.5–7.5
CRITICAL
7.5–10
5.0

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

What drove the Moderate classification for Green Tea Extract

GIRI Score 5.0 / 10

A score of 5.0 places this ingredient in the Moderate 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) 1 active signal

1 active signal (highest severity: High). 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.