No placebo control. Adverse effects ignored as "other viruses". Total of less than 1000 participants across eight trials--and only 342 were children who received the multivalent vaccine. This is not science.

*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)