MDA 2026 poster: Real-world safety of branded deflazacort in patients with Duchenne muscular dystrophy in the US: an analysis of the FAERS database
This poster, presented at MDA 2026, highlights real-world safety data for the branded formulation of deflazacort in patients with Duchenne muscular dystrophy (DMD) using reports from the FDA Adverse Event Reporting System (FAERS) database
- Learn about the safety profile of the branded formulation of deflazacort across nearly 18,000 patient-years of exposure
- Understand the most commonly reported adverse events and how they align with the known safety profile of corticosteroids
- Review real-world findings supporting the continued use and tolerability of the branded formulation of deflazacort in patients with DMD
Registration conditions vary by country; please consult local prescribing information and/or the Summary of Product Characteristics prior to prescribing any products.
MED-ALL-DFZ-2500002 v-2 | April 2026
This poster was developed and funded by PTC Therapeutics for MDA 2026.
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