ოთხშაბათი, აპრილი 15, 2026
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Global Ingredient Risk Index Weight Loss

Caralluma Fimbriata

Caralluma fimbriata

Also known as: Caralluma, Slimaluma, Caralluma extract, Indian Hoodia, Caralluma adscendens

LOW RISK 3.0/10 How?

Evidence Strength: LIMITED

This ingredient is classified as unclassified risk (GIRI score: 3.0/10). The classification is based on mechanistic and clinical evidence: caralluma fimbriata is believed to work by inhibiting the activity of citrate….

02

Safety Profile

Common Adverse Effects

  • Gastrointestinal discomfort
  • nausea
  • constipation
  • flatulence
  • headache

Serious Adverse Effects

  • Allergic reactions
  • severe gastrointestinal upset
  • potential hepatotoxicity

Contraindications

  • Pregnancy
  • breastfeeding
  • liver disease
  • kidney disease
  • People taking Antidiabetic drugs
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03

Interactions

Drug / Nutrient Interaction Mechanism Warning
Antidiabetic drugs potential additive effect — monitor blood glucose levels. Antihypertensive drugs: possible interaction — monitor blood pressure. CNS depressants: additive sedative effect — use with caution. Monitor
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04

Evidence and Scientific Findings

Overview

Ingredient Overview

Caralluma fimbriata is a succulent plant belonging to the Apocynaceae family, traditionally used in Indian medicine for its appetite-suppressing properties. It is commonly found in arid regions of India and is consumed as a vegetable or pickle. In dietary supplements, it is primarily used for weight loss due to its potential to reduce hunger and enhance satiety.
Classification

Biological and Chemical Classification

Chemical Class
Glycoside
Biological Class
Appetite suppressant
Natural Source
Caralluma fimbriata, aerial parts
Scientific Name
Caralluma fimbriata
Chemical Formula
Not applicable
CAS Number
Not applicable
Mechanism

Mechanism of Action

Caralluma fimbriata is believed to work by inhibiting the activity of citrate lyase, an enzyme involved in fat synthesis, thereby reducing fat accumulation. It may also influence the hypothalamus to suppress appetite by increasing serotonin levels. Additionally, it is thought to enhance energy expenditure, contributing to weight loss.
Clinical Evidence

Clinical Evidence of Effectiveness

Indication Evidence Level Summary
General Moderate Several small-scale human trials have investigated the effects of Caralluma fimbriata on weight loss. Results suggest modest reductions in body weight and waist circumference, particularly in overweight individuals. However, the studies are limited by small sample sizes and short durations, necessitating further research to confirm these findings.
Evidence levels: Strong Moderate Limited Experimental
Pharmacokinetics

Pharmacokinetics

Absorption
Oral absorption of Caralluma fimbriata is not well-characterized, but it is generally considered to have low bioavailability. The onset of action for appetite suppression is typically observed within a few hours of ingestion.
Distribution
Specific data on the distribution of Caralluma fimbriata in the body is lacking. It is presumed to have limited distribution due to its low bioavailability and potential for protein binding.
Metabolism
The metabolic pathways of Caralluma fimbriata have not been extensively studied. It is likely metabolized in the liver, but specific enzymes and metabolites remain unidentified.
Excretion
Excretion pathways for Caralluma fimbriata are not well-documented. It is presumed to be excreted primarily via the renal route, with some biliary excretion possible.
Dosage

Recommended Dosage

Condition / Use Typical Dose
Weight loss 500 mg twice daily. Appetite suppression: 1,000 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 70/100
Risk Level Moderate risk
Scientific Confidence High
Evidence Strength Moderate
Key Benefit Caralluma fimbriata is a succulent plant belonging to the Apocynaceae family, traditionally used in Indian medicine for its…
Key Safety Concern Caralluma fimbriata is generally considered safe for short-term use. However, caution is advised in pregnant or breastfeeding women due to insufficient safety data. Individuals with liver or kidney impairment should consult a healthcare provider before use. Regulatory bodies have not raised significant safety concerns, but long-term safety data is lacking.
Evidence Reviewed 10 PubMed studies
Scientific Confidence High
Based on study quality, consistency, and recency

Executive Summary — Ingredient Assessment

SETI Score 70/100
Risk Level Moderate risk
Evidence Strength Moderate
Main Benefit Caralluma fimbriata is a succulent plant belonging to the Apocynaceae family, traditionally used in Indian medicine for its…
Main Safety Concern Caralluma fimbriata is generally considered safe for short-term use. However, caution is advised in pregnant or breastfeeding women due to insufficient safety data. Individuals with liver or kidney impairment should consult a healthcare provider before use. Regulatory bodies have not raised significant safety concerns, but long-term safety data is lacking.
Ingredient Caralluma Fimbriata
Scientific name Caralluma fimbriata
Scientific Evidence Overview
  • 10 studies reviewed
  • 3 high-quality studies (meta-analysis or RCT)
  • Main clinical benefit observed: Caralluma fimbriata is a succulent plant belonging to the Apocynaceae family, traditionally used in Indian medicine for its…
  • Evidence consistency: High consistency across studies (100%)
Safety Signals
  • Caralluma fimbriata is generally considered safe for short-term use. However, caution is advised in pregnant or breastfeeding women due to insufficient safety data. Individuals with liver or kidney impairment should consult a healthcare provider before use. Regulatory bodies have not raised significant safety concerns, but long-term safety data is lacking.
Evidence Strength Moderate
Regulatory Status
  • USA/FDA — Approved
Final Scientific Assessment

Current scientific evidence suggests potential clinical benefits for Caralluma Fimbriata; however, some safety concerns have been reported in the literature. Additional large-scale randomized clinical trials are needed to confirm long-term safety and effectiveness.

Ingredient Caralluma Fimbriata
Evidence reviewed 10 peer-reviewed studies (last 10 years)
Scientific name Caralluma fimbriata
70 /100

Total SETI Score

Moderate risk
Evidence quality 30/40
Evidence consistency 20/20
Safety signals 0/20
Study recency 10/10
Evidence transparency 10/10

Evidence Summary

  • 10 studies reviewed
  • 3 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, 12:00

Evidence Distribution

2 Meta-analyses
1 Systematic reviews
3 Animal studies
4 Other / unclassified
  1. Observational / other LOW evidence YELLOW
    Potential use of titanium nano-gel to palliate redox status, DNA damage, histopathological changes, and renal-hepatic disorders induced by Candida albicans in Clarias… ↗
    Journal Vet Res Commun
    Year 2025
    Study type Observational / other
    Evidence strength LOW evidence
    Thabet RY et al.. Potential use of titanium nano-gel to palliate redox status, DNA damage, histopathological changes, and renal-hepatic disorders induced by Candida albicans in Clarias gariepinus.. Vet Res Commun. 2025. PMID:40944746.
  2. Animal study LOW evidence YELLOW
    Exploring the antiarthritic potential of Caralluma fimbriata: Phytochemical screening and preliminary observations in a rat model. ↗
    Journal J Ethnopharmacol
    Year 2025
    Study type Animal study
    Evidence strength LOW evidence
    Mali KK et al.. Exploring the antiarthritic potential of Caralluma fimbriata: Phytochemical screening and preliminary observations in a rat model.. J Ethnopharmacol. 2025. PMID:40816583.
  3. Observational / other LOW evidence YELLOW
    Cricket protein-based film containing Caralluma fimbriata extract-based nanoparticles for preservation of cheddar cheese. ↗
    Journal Ultrason Sonochem
    Year 2025
    Study type Observational / other
    Evidence strength LOW evidence
    Lone AB et al.. Cricket protein-based film containing Caralluma fimbriata extract-based nanoparticles for preservation of cheddar cheese.. Ultrason Sonochem. 2025. PMID:39616721.
  4. Animal study LOW evidence YELLOW
    Caralluma fimbriata Extract Improves Vascular Dysfunction in Obese Mice Fed a High-Fat Diet. ↗
    Journal Nutrients
    Year 2024
    Study type Animal study
    Evidence strength LOW evidence
    Thunuguntla VBSC et al.. Caralluma fimbriata Extract Improves Vascular Dysfunction in Obese Mice Fed a High-Fat Diet.. Nutrients. 2024. PMID:39770917.
  5. Animal study LOW evidence YELLOW
    Exploring the therapeutic potential of Caralluma fimbriata for antioxidant and diabetes management: a 28-day rat model study. ↗
    Journal Toxicol Res (Camb)
    Year 2024
    Study type Animal study
    Evidence strength LOW evidence
    Arif A et al.. Exploring the therapeutic potential of Caralluma fimbriata for antioxidant and diabetes management: a 28-day rat model study.. Toxicol Res (Camb). 2024. PMID:38957782.
  6. Observational / other LOW evidence YELLOW
    Delving the Role of Caralluma fimbriata: An Edible Wild Plant to Mitigate the Biomarkers of Metabolic Syndrome. ↗
    Journal Oxid Med Cell Longev
    Year 2022
    Study type Observational / other
    Evidence strength LOW evidence
    Anwar R et al.. Delving the Role of Caralluma fimbriata: An Edible Wild Plant to Mitigate the Biomarkers of Metabolic Syndrome.. Oxid Med Cell Longev. 2022. PMID:35770046.
  7. Systematic review HIGH evidence YELLOW
    Modulation of the hypothalamic-pituitary-adrenal (HPA) axis by plants and phytonutrients: a systematic review of human trials. ↗
    Journal Nutr Neurosci
    Year 2022
    Study type Systematic review
    Evidence strength HIGH evidence
    Lopresti AL et al.. Modulation of the hypothalamic-pituitary-adrenal (HPA) axis by plants and phytonutrients: a systematic review of human trials.. Nutr Neurosci. 2022. PMID:33650944.
  8. Meta-analysis HIGH evidence YELLOW
    The use of Caralluma fimbriata as an appetite suppressant and weight loss supplement: a systematic review and meta-analysis of clinical trials. ↗
    Journal BMC Complement Med Ther
    Year 2021
    Study type Meta-analysis
    Evidence strength HIGH evidence
    Jayawardena R et al.. The use of Caralluma fimbriata as an appetite suppressant and weight loss supplement: a systematic review and meta-analysis of clinical trials.. BMC Complement Med Ther. 2021. PMID:34758791.
  9. Observational / other LOW evidence YELLOW
    The effect of an orally-dosed Caralluma Fimbriata extract on appetite control and body composition in overweight adults. ↗
    Journal Sci Rep
    Year 2021
    Study type Observational / other
    Evidence strength LOW evidence
    Rao A et al.. The effect of an orally-dosed Caralluma Fimbriata extract on appetite control and body composition in overweight adults.. Sci Rep. 2021. PMID:33762661.
  10. Meta-analysis HIGH evidence YELLOW
    Effect of the herbal medicines in obesity and metabolic syndrome: A systematic review and meta-analysis of clinical trials. ↗
    Journal Phytother Res
    Year 2020
    Study type Meta-analysis
    Evidence strength HIGH evidence
    Payab M et al.. Effect of the herbal medicines in obesity and metabolic syndrome: A systematic review and meta-analysis of clinical trials.. Phytother Res. 2020. PMID:31793087.
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06

Score Transparency

Q × L × D × S × 10 = 3.0 / 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 5 / 10
50%

One or more monitoring-level safety signals active

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 × 5S = 3.0 / 10

Final GIRI Score for Caralluma Fimbriata. 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

LOW RISK 3.0/10

Based on available regulatory signals and scientific evidence, this ingredient presents a low safety concern under normal conditions of use.

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

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

What drove the Low classification for Caralluma Fimbriata

GIRI Score 3.0 / 10

A score of 3.0 places this ingredient in the Low 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) 0 active signals

No active signals — S component is at neutral baseline (0.5), contributing no extra risk weight.

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.