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Florastor is the Optimal Probiotic Choice for Patients in Healthcare Facilities
Check Icon Enhances quality of care: Helps reduce the risk of GI issues associated with antibiotic use
Check Icon Improves Healthcare Facility Budgets: Reduces the need for incontinence management, supplies and linens during antibiotic therapy
Check Icon Streamline patient care:
Florastor can be co-administered with antibiotics, unlike most bacteria-based probiotics that require staggered dosing, saving time and simplifying patient care
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Contact Aldo Mistretta (a.mistretta@biocodex.com) for more information.

Florastor® Safety Warning
Do not use Florastor or other probiotics in any ICU setting and in those individuals with open arterial and venous access required (such as a Vascath, Permcath, or AV fistula). Do not use for any individual with a central line or port or in the surroundings of any patient with a central line or port. [Central lines include short- and long-term central venous catheters (CVCs) and peripherally inserted central catheters (PICCs)]. Do not use Florastor for pre- or post- organ or bone marrow transplant patients and other patients considered severely immunocompromised or critically ill. Do not use in pre-term or neonatal infants under 2 months of age. Do not use Florastor probiotics if allergic to any components (especially yeast). Less than 1% of patients experience constipation or thirst. Very rarely, side effects such as: allergic reaction (skin rash). Fungemia or sepsis in patients with a central venous catheter, and in hospitalized, immunocompromised patients may occur.

For product questions or to report an adverse event, please call 877-356-7787.

This educational information is intended for use by qualified healthcare practitioners only and is not intended for use by consumers or to substitute for appropriate professional care.

† In Value. Reference on File.

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Florastor (S. boulardii CNCM I-745®) is manufactured and distributed exclusively by Biocodex, the worldwide leader in microbiota research.

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