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[7] Because retatrutide is an IMP, the storage conditions that apply to any given supply will be specified on the IMP label and in the clinical trial protocol or named-patient supply documentation
Making this a much more cost effective and affordable option
A narrative review concluded that the practice is controversial because there are no standardized dosing protocols and nearly onethird of patients report adverse effects, ranging from mild gastrointestinal symptoms to liver dysfunction and lifethreatening allergic reactions
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