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Drug Imports Alerts Database FDA Import Alerts notify field staff and the public when the agency has enough evidence to detain products without physical examination (DWPE) due to suspected violations of FDA laws, including violations of current good manufacturing practices for finished pharmaceuticals or unapproved new drugs
Individuals who used GLP-1RAs for 0.5, 1, and 1.5 years had IRRs close to 1.0, with no significant decrease in MACE risk at three years, although these estimates varied across specific treatment strategies defined by prior duration and subsequent exposure patterns
Therapeutic Goods Administration (TGA), 2 December 2020
Consistent documentation provides objective evidence of medication efficacy, helps identify patterns between lifestyle factors and outcomes, and enables early recognition of adverse effects requiring intervention
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