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American Journal Of Physiology

15: 100181 Karagounis L, Hawley J

Outcome The primary outcome was to assess the incidence of new-onset adverse CVEs, which were categorised as: (1) heart failure

The FDA has expressed willingness to provide regulatory flexibility toward compounders that keep filling requests that were made prior to the shortage ending

Incorrect Dosing and Side Effects Without baseline metabolic data: Dosing may be too aggressive Side effects (nausea, fatigue) may be exacerbated False Sense of Safety The logic often goes: If its FDA-approved, it must be safe for me. But FDA approval assumes appropriate patient selection and monitoringnot universal applicability without evaluation