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Methods Patients and study design The study protocol was conducted in accordance with the guidelines contained within the Declaration of Helsinki and was approved by the ethics committees of Yokohama City University and Kyoto Prefectural University of Medicine

At the highest tested dose (500 g/L), the proportion of Lactobacillus and Weissella significantly increases

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Food and Drug Administrations (FDA) Approved Drugs database does not include BPC-157 or any of its other names

Prophylactic Injections Coders must determine why the provider administered the injection

Lastly, each participant was given five quality of life (QOL) questionnaires (WHOQOL-BREF) to fill out at home for the duration of the study [22]