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The most common adverse events are gastrointestinal: nausea (occurring in 12-33% of subjects depending on dose), diarrhea, constipation, and decreased appetite
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Specialized toxicology research shows no embryo-fetal developmental toxicity, no genetic mutagenicity in bacterial and mammalian cell assays, and no adverse reproductive effects in animal models
Common Protocol: BPC-157: 250500 mcg daily, subcutaneous near injury or systemic TB500: 25 mg per week, split into 23 injections Cycle: 46 weeks, followed by reassessment 2
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