Tag: adverse event reporting

Clinical Trial Data vs Real-World Side Effects: What You Need to Know

Clinical trial data shows how a drug performs under ideal conditions, but real-world side effects reveal what actually happens when millions of people use it. Learn the key differences and why both matter for your health.

Post-Market Studies on Generic Drug Safety: What Happens After Approval

Generic drugs are safe for most people, but because they're approved without large clinical trials, hidden safety issues can emerge after they're widely used. Learn how the FDA tracks problems, why some patients react differently to generics, and what you can do to stay safe.