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The company stopped making the drug in 2021, after the FDA began requiring pharmacies to obtain a new license to produce it

Serious Adverse Events Seizures: There have been reports of increased seizure frequency in patients with a pre-existing seizure disorder

This points to the possibility that the peptide could influence extracellular matrix maintenance, hydration, and skin barrier strength in laboratory settings

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Pawlak, R., Lester, S