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Current human safety data obtained under approved therapeutic regimens are characterized predominantly by mild-to-moderate gastrointestinal adverse events rather than generalized cytotoxic toxicity, underscoring the need to distinguish preclinical pro-apoptotic observations from clinically established safety profiles

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In Canada, prescription drugs include both active and inactive ingredients, and while a name-brand drugs active ingredients may be the same as a generics, inactive ingredients (also called excipients) may differ

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