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Comprehensive review of cardiovascular toxicity of drugs and related agents

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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%

Because AOD-9604 does not affect appetite, energy levels, or other subjectively perceptible parameters, this initial period may feel unchanged