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What the Trials Reported About Tolerability and Safety The adverse events reported most often were gastrointestinal nausea, vomiting, diarrhea, and constipation characterized as predominantly mild to moderate, dose-dependent, and concentrated during escalation
After the 30-day treatment period, biochemical parameters were analyzed in the pancreas, liver, and serum
Moreover, growth rates of humanized E
coli for GPI with the mutant GPI s to investigate activity differences
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