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Concerns include reports of adverse events, some requiring hospitalization, that may be related to dosing errors or doses beyond what is in the FDA-approved drug label, which means using more product in a single dose, taking doses more frequently or increasing the amount more quickly (titration schedule)

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[DOI] [PubMed] [Google Scholar] 25.Chimerel C., Emery E., Summers D.K., Keyser U., Gribble F.M., Reimann F