Table 2_Safety assessment of laronidase: real-world adverse event analysis based on the FDA adverse event reporting system (FAERS).xlsx
Objective<p>Laronidase is the first drug of enzyme replacement therapy approved for the treatment of mucopolysaccharidosis type I (MPS I). However, its adverse events (AEs) have not been investigated in real - world settings. The aim of this study was to investigate AEs associated with laronid...
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2025
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