FDA Drug Safety Labeling Changes
Food and Drug Administration (FDA) announces important safety label changes for prescription drugs almost every month. By implementing the label changes the FDA warns a physician of new side- effects, adverse reactions, contra-indications and precautions necessary for a drug. This information is important for safe practice of medicine.
2016 - Monthly Summary Report for Drug Label Changes
2015 - Monthly Summary Report for Drug Label Changes
2014 - Monthly Summary Report for Drug Label Changes
2013 - Monthly Summary Report for Drug Label Changes
2012 - Monthly Summary Report for Drug Label Changes
