Topic: azipro

These reports of adverse events have prompted many patients to file a Lipitor lawsuit against the drug manufacturer. The FDA sent a 12-page letter of rebuke to Pfizer in June 2010, alleging that the company had a six-year history of failing to send along adverse event reports in a timely manner. The FDA requires that these reports be submitted within 15 days of receipt. The U.S. Food and Drug Administration (FDA) is supposed to ensure the safety and quality of drugs reaching the public, acting ...