retatrutide approval fda 2025 Letter regarding ilanamuhlsteinrd Everyone is asking me
Description
The FDA has distinguished between mass-marketed compounded products and patient-specific compounding performed under Section 503A of the FD&C Act, which may remain permissible in narrow circumstances where a patient's medical needs cannot be met by an FDA-approved drug
While they use the same active ingredient, equivalence to FDA-approved finished products should not be assumed

Severe nausea, vomiting, and diarrhea can cause dangerous dehydration, and overdosing can trigger complications like pancreatitis or gallbladder problems

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