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The FDA noted that it had received over 1000 reports of adverse events arising from compounded GLP-1 dosing errors and unapproved ingredients and suggested that such adverse events are likely underreported due to the limited application of federal regulations to state-licensed pharmacies
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That raises the prospect, she said, that patients will stop taking the drugs and regain weight, which will lead to poor clinical outcomes. Join our commenting forum Join thought-provoking conversations, follow other Independent readers and see their replies Comments
The FDA has been vocal about its concerns in this category
Keep separate vials for separate peptides if needed
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