FDA issues warning against Pfizer for failure to report side effects

In response to a six week long audit of Pfizer’s New York headquarters last summer, the FDA has recently issued what has been decribed as a "stinging" 12-page letter scolding Pfizer for failing to meet regulatory deadlines for reporting serious side effects with many of its drugs, including Lipitor, Selzentry, Lyrica, Camptosar and Viagra. Go here for the full story. Go here for a copy of the letter.