The Nation - News from July 4, 1986
The Food and Drug Administration issued a new rule that will require makers of prescription drugs--new and old--to report adverse reactions to their products. The reporting of adverse reactions until now has been a requirement for new drugs only, primarily those that have been brought to market since 1938, the FDA said. That includes about 90% of prescription drugs sold but leaves out 4,000 products.
More to Read
Start your day right
Sign up for Essential California for news, features and recommendations from the L.A. Times and beyond in your inbox six days a week.
You may occasionally receive promotional content from the Los Angeles Times.