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Each review contains information about the ingredient’s clinical applications, formulations, dosing & administration, adverse effects, and pharmacokinetics. Learn more about our critical appraisal research or contact us for initial guidance and more information.

Saccharomyces boulardii

Saccharomyces boulardii (S. boulardii) is a non-pathogenic yeast microbe with properties that protect it against antibiotics, the body’s internal temperatures, and the acidic environments of the gastrointestinal tract. These properties are not typically observed with bacterial probiotics. (2)(9S. boulardii was first discovered in lychee and mangosteen fruit and is now cultivated for use in supplements as lyophilized powders, capsules, or liquid beverages. (5

Not to be confused withSaccharomyces cerevisiae (7)

Main uses

  • Diarrhea
  • Gastrointestinal disorders
  • Parasitic infections

Formulations

Preparation Stability
Heat-dried
Labels typically indicate the requirement of refrigeration to prevent loss of potency (7)
Lyophilized
Stable at room temperature if kept free from moisture (7)
May have better survival against bile and stomach acid (4)

Dosing & administration

Acute diarrhea
General outcomes from A-level evidence

No data currently available.

Dosing & administration

500-750 mg w/ concurrent therapy, 8-10 days

Outcomes

↓ diarrhea severity score, Entamoeba histolytica dysentery (7)
Class of evidence


A

Antibiotic-associated diarrhea
General outcomes from A-level evidence
No data currently available.
Dosing & administration
500-1000 mg w/ concurrent therapy, + 2 weeks

Outcomes

↑ prevention of AAD (7)
Class of evidence


A

Dosing & administration
Children: 250-500 mg w/ concurrent therapy Adults: up to 1000 mg w/ concurrent therapy

Outcomes

↓ risk of AAD from 20.9% to 8.8%
↓ risk of AAD from 17.4% to 8.2% (8)
 
Class of evidence


A

Clostridium difficile
General outcomes from A-level evidence
No data currently available.
 
Dosing & administration
1000 mg w/ concurrent therapy, 4 weeks

Outcomes

↓ C. difficile recurrence post-eradication (7)

Class of evidence

A

Giardiasis
General outcomes from A-level evidence
No data currently available.
 
Dosing & administration
500 mg w/ concurrent therapy, 4 weeks

Outcomes

↓ giardia cyst count (1)

Class of evidence

B

Helicobacter pylori
General outcomes from A-level evidence
No data currently available.
 
Dosing & administration
1000 mg w/ concurrent therapy, 2 weeks

Outcomes

↓ epigastric distress, global dyspepsia symptom scores, AAD (7)

Class of evidence

A

HIV-related diarrhea
General outcomes from A-level evidence
No data currently available.
 
Dosing & administration
3000 mg, 7 days

Outcomes

↓ diarrhea frequency (7)

Class of evidence

A

Inflammatory bowel disease
General outcomes from A-level evidence
No data currently available.
 
Dosing & administration
750-1000 mg w/ concurrent therapy, 7 weeks-6 months

Outcomes

↓ ulcerative colitis, Crohn’s bowel movements, relapse in Crohn’s treatment (7)
 
Class of evidence


A

Dosing & administration
100 mg w/ concurrent therapy, 3 months

Outcomes

↓ intestinal permeability in Crohn’s (3)
Class of evidence


C

Irritable bowel syndrome
General outcomes from A-level evidence
May improve hyperandrogenemia, ovarian histomorphology, folliculogenesis, and luteinisation processes, as well as insulin resistance and chronic inflammation (58)
 
Dosing & administration
500 mg, 4 weeks
Outcomes
↓ bowel movements, global IBS symptoms (7)
Class of evidence


A

Nutrient-associated diarrhea
General outcomes from A-level evidence
No data currently available.
 
Dosing & administration
2000 mg, 8-28 days

Outcomes

↓ occurrence of diarrhea and number of days (7)
Class of evidence


A

Adverse effects

S. boulardii is generally regarded as safe, however, an increased risk of non-infectious adverse effects (e.g., biliary tract stenoses, fistulas, lienalis-steal syndrome, abdominal hemorrhage, and acute renal failure) has been found in specific groups (e.g., immunocompromised patients, transplant patients or patients with pancreatitis). Rare cases of fungemia associated with S. boulardii have also been reported. (6)(7)(10)

Pharmacokinetics

Absorption

  • S. boulardii is not absorbed, but concentrations stabilize within three days of oral ingestion. (6)(7)

Distribution

  • Survives in the intestinal tract to reach the colon, its most common target. (6)

Metabolism

  • S. boulardii is not metabolized but rather dies within the competitive environment of the gastrointestinal tract and is excreted. Levels found excreted in the stool can be 100-1000 times smaller than the ingested dose. (6)

Excretion

  • With a half-life of six hours, S. boulardii populations may clear after three to five days after discontinuation in the feces. (6)(7)
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