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It evaluates seven key factors: timing of drug exposure, improvement after stopping the drug, patient risk factors, exclusion of other liver diseases, known drug hepatotoxicity, recurrence after re-exposure, and interactions with other medications (Table 6)

Any compound that potentiates this pathway carries a theoretical risk of promoting neoplastic processes (PMID: 34179015) No Chronic Toxicity Data: Long-term effects of sustained HGF/c-Met potentiation are unstudied even in animal models Uncharacterized Dose-Response: The relationship between Dihexa dose and adverse effects in any living system is poorly defined beyond acute preclinical studies No Regulatory Review: Dihexa has never undergone the systematic safety evaluation required for regulatory submission Safety Comparison Summary: Cerebrolysin has a known, well-characterized safety profile from decades of clinical use

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Are there known drug interactions

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