ორშაბათი, აპრილი 13, 2026
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Global Ingredient Risk Index Botanical

Senna

Senna alexandrina (Cassia senna)

Also known as: alexandrian senna, tinnevelly senna, cassia senna, sennosides

HIGH RISK 7.5/10 How?

This ingredient is classified as unclassified risk (GIRI score: 7.5/10).

02

Safety Profile

Known Safety Concerns

  • Chronic use: cathartic colon, laxative dependency
  • Electrolyte depletion -- hypokalemia, cardiac risk
  • Hepatotoxicity with chronic use
  • Frequently misused in weight-loss products
  • Contraindicated in IBD, intestinal obstruction
  • FDA warnings for senna-containing supplement products

Contraindications

  • Chronic use: cathartic colon, laxative dependency
  • Electrolyte depletion -- hypokalemia, cardiac risk
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03

Interactions

Information not yet available for this ingredient profile.

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04

Evidence and Scientific Findings

Overview

Ingredient Overview

Senna is an anthraquinone stimulant laxative approved for short-term constipation. Chronic use causes cathartic colon syndrome, electrolyte depletion (hypokalemia), and hepatotoxicity. Popular in weight-loss supplements and detox teas — frequently misrepresented. FDA has warned about senna in dietary supplements.

Classification

Biological and Chemical Classification

Scientific Name
Senna alexandrina (Cassia senna)
Mechanism

Mechanism of Action

Information not yet available for this ingredient profile.

Clinical Evidence

Clinical Evidence of Effectiveness

Information not yet available for this ingredient profile.

Pharmacokinetics

Pharmacokinetics

Information not yet available for this ingredient profile.

Dosage

Recommended Dosage

Information not yet available for this ingredient profile.

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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 Botanical
Key Safety Concern Chronic use: cathartic colon, laxative dependency
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 Botanical
Main Safety Concern Chronic use: cathartic colon, laxative dependency
Ingredient Senna
Scientific name Senna alexandrina (Cassia senna)
Scientific Evidence Overview
  • 10 studies reviewed
  • 0 high-quality studies (meta-analysis or RCT)
  • Main clinical benefit observed: Botanical
  • Evidence consistency: High consistency across studies (100%)
Safety Signals
  • Chronic use: cathartic colon, laxative dependency
  • Electrolyte depletion -- hypokalemia, cardiac risk
  • Hepatotoxicity with chronic use
  • Frequently misused in weight-loss products
  • Contraindicated in IBD, intestinal obstruction
Evidence Strength Limited
Final Scientific Assessment

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

Ingredient Senna
Evidence reviewed 10 peer-reviewed studies (last 10 years)
Scientific name Senna alexandrina (Cassia senna)
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: 25 მარ 2026, 22:41

Evidence Distribution

10 Other / unclassified
  1. Observational / other LOW evidence YELLOW
    Adding Senna alkaloid to laxative agents in bowel preparation for pediatric colonoscopy: a clinical trial study. ↗
    Journal Arab J Gastroenterol
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Mahdavi Mortazavi SM et al.. Adding Senna alkaloid to laxative agents in bowel preparation for pediatric colonoscopy: a clinical trial study.. Arab J Gastroenterol. 2026. PMID:41866261.
  2. Observational / other LOW evidence YELLOW
    Laxative use and acute kidney injury risk: Analysis of a Japanese hospital-based database. ↗
    Journal J Pharmacol Exp Ther
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Mitsuboshi S et al.. Laxative use and acute kidney injury risk: Analysis of a Japanese hospital-based database.. J Pharmacol Exp Ther. 2026. PMID:41806409.
  3. Observational / other LOW evidence YELLOW
    Inter-Laboratory Comparison of Photometric and LC Assay Methods for Hydroxyanthracene Glycosides Determination in Senna Herbal Drugs and Dry Extracts. ↗
    Journal Planta Med
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Peter S et al.. Inter-Laboratory Comparison of Photometric and LC Assay Methods for Hydroxyanthracene Glycosides Determination in Senna Herbal Drugs and Dry Extracts.. Planta Med. 2026. PMID:41802773.
  4. Observational / other LOW evidence YELLOW
    Towards an attract-and-kill strategy for sustainable tick control: combined effects of Metarhizium anisopliae and phytochemical attractants from Senna didymobotrya against Amblyomma variegatum… ↗
    Journal Exp Appl Acarol
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Kinyua DW et al.. Towards an attract-and-kill strategy for sustainable tick control: combined effects of Metarhizium anisopliae and phytochemical attractants from Senna didymobotrya against Amblyomma variegatum and Rhipicephalus appendiculatus.. Exp Appl Acarol. 2026. PMID:41792543.
  5. Observational / other LOW evidence YELLOW
    The anti-obesity potential of Cassiae Semen: A review based on ethnopharmacology and modern pharmacology. ↗
    Journal J Ethnopharmacol
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Ye Y. The anti-obesity potential of Cassiae Semen: A review based on ethnopharmacology and modern pharmacology.. J Ethnopharmacol. 2026. PMID:41791619.
  6. Observational / other LOW evidence YELLOW
    Phytosociological analysis and floristic composition of fabaceae species assessing human impact and edaphic variables. ↗
    Journal Sci Rep
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Majeed M et al.. Phytosociological analysis and floristic composition of fabaceae species assessing human impact and edaphic variables.. Sci Rep. 2026. PMID:41786781.
  7. Observational / other LOW evidence YELLOW
    Dataset on MatK chloroplast gene sequences of five underutilized nigerian native legume species. ↗
    Journal Data Brief
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Olaoluwa FD et al.. Dataset on MatK chloroplast gene sequences of five underutilized nigerian native legume species.. Data Brief. 2026. PMID:41783791.
  8. Observational / other LOW evidence YELLOW
    Jiawei YigongSan improves gastric motility and is associated with modulation of PI3K/Akt/mTOR signaling and autophagy in a rat model of functional dyspepsia. ↗
    Journal J Ethnopharmacol
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Wang X et al.. Jiawei YigongSan improves gastric motility and is associated with modulation of PI3K/Akt/mTOR signaling and autophagy in a rat model of functional dyspepsia.. J Ethnopharmacol. 2026. PMID:41713812.
  9. Observational / other LOW evidence YELLOW
    Improving Constipation in Critical Care Patients: A Single-Centre Prospective Cohort Closed-Loop Clinical Audit. ↗
    Journal Cureus
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Xu N et al.. Improving Constipation in Critical Care Patients: A Single-Centre Prospective Cohort Closed-Loop Clinical Audit.. Cureus. 2026. PMID:41669582.
  10. Observational / other LOW evidence YELLOW
    Preclinical evaluation of Senna alata leaf extract against Hymenolepis diminuta: a promising natural anthelmintic solution. ↗
    Journal BMC Complement Med Ther
    Year 2026
    Study type Observational / other
    Evidence strength LOW evidence
    Roy S et al.. Preclinical evaluation of Senna alata leaf extract against Hymenolepis diminuta: a promising natural anthelmintic solution.. BMC Complement Med Ther. 2026. PMID:41664129.
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06

Score Transparency

Q × L × D × S × 10 = 7.5 / 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 = 7.5 / 10

Final GIRI Score for Senna. 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 7.5/10

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
7.5

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

What drove the High classification for Senna

GIRI Score 7.5 / 10

A score of 7.5 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) 0 active signals

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

Regulatory Status No restrictions found

No major regulatory restrictions or advisories recorded across monitored jurisdictions (FDA, EMA, Health Canada, TGA, and others).

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.