Tag: FDA adverse event reporting
The FDA monitors generic drug safety after approval through real-time reporting, manufacturing data, and patient feedback. Learn how adverse events are tracked, what gaps exist, and what’s changing in 2025 to improve detection of quality and effectiveness issues.
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Chest Pain Evaluation: When to Go to the Emergency Department
Jan, 13 2026
Vanadium: The Dietary Supplement You Didn't Know You Needed
Sep, 4 2023
Corticosteroid Injections for Joint Pain: What They Do, How Long They Last, and When to Avoid Them
Jan, 5 2026
Inactive Ingredient Differences: Why Your Generic Medication May Feel Different
Nov, 22 2025
Candidemia & Disseminated Candida Infections: Why Patient Education Matters
Oct, 21 2025