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Specifically, the FDA considered claims that compounded products are generic versions or contain the same active ingredient as FDA-approved GLP-1 drugs are false or misleading

This increases the risk that: Products may be contaminated or mislabeled Adverse events may not be monitored or reported Patients may be misled about efficacy 4

It's important to note that menstrual outcomes were not primary endpoints in major GLP-1 clinical trials, and much of the current understanding comes from post-marketing surveillance and patient reports

Can I Take Humanin with a GLP-1 Medication

Q: Is a prescription required for POLYBION INJECTION