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Storage typically requires refrigeration before first use and room-temperature windows afterward, following the specific product label

Regulatory agencies, including the US Food and Drug Administration, the European Medicines Agency, and the Pharmaceuticals and Medical Devices Agency, require extensive Phase III clinical trials, immunogenicity assessments, and comprehensive Chemistry, Manufacturing, and Controls data before approving new GLP-1 therapies or label expansions

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Severe stomach pain that radiates to your back requires immediate medical attention