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Description

The Phase II clinical trial in postoperative ileus patients established that IV ipamorelin at 0.03 mg/kg twice daily for up to 7 days was well-tolerated with no significant adverse events compared to placebo (Beck et al., 2014)

The FDA prescribing information identifies serious hypersensitivity as a contraindication to continued use

In addition, health systems and insurance providers are actively reviewing policies regarding obesity treatment

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