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Through the FDA Adverse Event Reporting System (FAERS), healthcare providers and patients can report suspected adverse events, including potential malignancies, enabling the agency to detect safety signals that may not have been apparent in pre-approval clinical trials

Neurological Protection: Preliminary research in animal models suggests potential neuroprotective effects, although human data is lacking

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LEF1, Ki67, and c-Myc were upregulated in the dorsal skin of mice after treatment