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In 2024, the FDA updated Ozempics label to warn of a risk of pulmonary aspiration in patients who undergo procedures or surgeries requiring deep sedation or anesthesia

The FDA has not reviewed, approved, or stamped that specific compounded preparation for safety, effectiveness, or quality

This proactive approach aims not only to address current concerns but also to prevent future legal challenges by refining their product offerings

Instead, it is a response to rapid changes the body is undergoing

Keeping a symptom diary noting the frequency, severity, and any associated symptoms can provide valuable information for clinical assessment