Everyday, millions of Americans take prescription and over-the-counter medications and supplements with the expectation of improving or maintaining their health. Unfortunately, even with government oversight and drug research, these daily doses can become “adverse drug events,” causing additional and/or more complex health problems or even death.
The Institute for Safe Medication Practices reported that adverse drug events increased sharply, hitting record numbers in the first quarter of 2008. According to the report:
- 20,745 cases of serious injuries were reported — the highest for any quarter reported in a calendar quarter since 2006
- 4,824 drug-related deaths were reported — the highest number of deaths reported since 2006
What is a serious adverse drug event?
A serious adverse drug event is one that causes death, birth defects, disability, puts someone in a hospital, or was life-threatening. The following is a list of pharmaceuticals that have been linked to serious side effects, including heart attacks, strokes, hypertension, seizures, liver problems and/or death.
Our Experience
Hance & Srinivasan are experienced at litigation involving adverse drug events.
If you or someone you love has been injured or died as result of a serious adverse drug event, please contact Hance & Srinivasan to discuss the individual nature of your situation.
At Hance & Srinivasan, we want you to be informed about all of the dangers of unsafe drugs and medications. We encourage you to visit the Food and Drug Administration (FDA) Website to recognize potential signals about serious risk associated with drugs and medications and also how to report drug injuries.
