Five months before the Food and Drug Administration issued a health warning on puberty blockers widely used off-label to treat minors with gender confusion, undermining a Department of Health and Human Services office that claimed "early gender affirming care is crucial to overall health and well-being," an FDA leader acknowledged other health concerns.
Pediatric patients exposed to "gonadotropin-releasing hormone agonists," most with central precocious puberty (CPP) and "a handful … transgender kids using the drugs off-label," had an "increased risk of depression and suicidality, as well as increased seizure risk," Division of General Endocrinology clinical team leader Shannon Sullivan told colleagues.
FDA Knew ‘Gender Affirming’ Puberty Blockers Increase ‘Suicidality’ in 2017, Promotes Them Today
