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Brandt-Jacobsen NH, Lav Madsen P, Johansen ML, Rasmussen JJ, Forman JL, Holm MR, et al

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2 mg subcutaneous daily for 26 weeks, n = 273 active arm): Pooled with injection-site reactions broadly defined (erythema, pruritus, pain, urticaria, hemorrhage, irritation), the total injection-site adverse event rate in the active arm was approximately 25%

By contrast, other GH-axis compounds occupy different regulatory positions: tesamorelin is FDA-approved for a narrow HIV-associated lipodystrophy indication, and sermorelin retains a special status from its prior FDA approval