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U.S. Department of Health and Human Services

Safety

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Lupron Depot - Ped (leuprolide acetate for depot suspension) Injection, powder for suspension

Detailed View: Safety Labeling Changes Approved By FDA Center for Drug Evaluation and Research (CDER) – August 2010

Summary View

 

ADVERSE REACTIONS

Clinical Trials
  • In two studies of children with central precocious puberty, in 2% or more of the patients receiving the drug, the following adverse reactions were reported to have a possible or probable relationship to drug as ascribed by the treating physician...(all available treatment-related adverse reaction data from the ongoing Study)
Postmarketing
  • Convulsion
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