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The agency also issued warning letters to a variety of drug and supplement makers, among them a Florida company that the FDA says supplied compounders with adulterated raw ingredients shipped by multiple companies listed on the agencys import alerts, a Delaware company selling children's supplements made with undeclared ibutamoren mesylate, a non-FDA-approved ingredient that can cause serious side effects, and a compounding pharmacy in Texas for current good manufacturing practice violations
Patients experiencing new or worsening mood symptoms should report them to their healthcare provider and through the FDA MedWatch program
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