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Phase I data and clinical experience report no serious adverse events at doses up to 10 mg per injection
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Characterization of two novel Intronic variants affecting splicing in FBN1-related disorders
Adverse Effects and Reporting Adverse events or suspected contamination issues should be reported immediately to the manufacturer (Hospira/Pfizer) and relevant regulatory authorities (FDA MedWatch, poison control, or institutional pharmacovigilance systems)
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