RFK, Jr. Discusses MMR "Safety" Trials Obtained Through FOIA

Press release from ICAN:
https://finance.yahoo.com/news/mmr-vaccine-licensing-called-following-131500482.html

The MMR vaccine is at the heart of the vaccine debate. The following are some of the key facts learned from the clinical trial reports produced by the FDA, which the agency relied upon to license the MMR:
• There were eight clinical trials that in total had less than 1,000 individuals, out of which only 342 children received the MMR vaccine 
• The safety review period only tracked ‘adverse events’ for 42 days after injection 
• More than half or a significant percent of all participants in each of the eight trials developed gastrointestinal symptoms and upper respiratory infections 
• All adverse events were generically described as ‘other viruses’ and not considered in safety profile of licensure 
• The control group received other vaccines for either rubella or measles and rubella, and none of the controls received a placebo (an inert substance such as a saline injection)