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Mandatory adverse event reporting: 503B facilities are required to report adverse events to the FDA, creating a safety surveillance system that parallels (though doesn't replicate) the pharmacovigilance systems used for FDA-approved drugs

The main job of this page is safety and side-effect planning, especially where the topic touches side effects

Schermer and colleagues aimed to investigate whether treatment with inhaled corticosteroid (fluticasone propionate) or oral NAC are effective in primary care patients

The Multifaceted Role of Glutathione S-Transferases in Health and Disease

10.1097/md.0000000000017997 Medicine (Baltimore)