From the ICAN website:

As explained in our prior update, v-safe is a new smartphone-based CDC program that allows users to register after getting a Covid-19 vaccine and provide health check-ins.

ICAN wanted to obtain this data. So, it deployed its legal team, headed by Aaron Siri, to obtain the v-safe data.

After suing the CDC twice, and following months of legal wrangling, the CDC finally capitulated, resulting in a court order that required it to produce this data. The first batch of data, containing 144 million rows of health entries by v-safe users, has now been obtained by ICAN and you can search it using a user-friendly interface that ICAN worked around the clock to create.

This first batch of data includes the responses v-safe users provided to pre-populated ‘check-the-box’ fields. It does not include data from the fields that allowed free-text responses. It nonetheless reveals shocking information that should have caused the CDC to immediately shut down its Covid-19 vaccine program.

Among numerous alarming results, out of the approximate 10 million individuals that registered and submitted data to v-safe, 782,913 individuals, or over 7.7% of v-safe users, had a health event requiring medical attention, emergency room intervention, and/or hospitalization. Over 25% had an event that required them to miss school or work and/or prevented normal activities.

There were also 71 million reports of symptoms in the pre-populated fields from the approximately 10 million users. This is an average of over 7 symptoms reported per v-safe registrant. Reported symptoms include, for example, over 4 million reports of joint pain, a very concerning immune reaction. While around 2 million of these joint pain reports were mild, over 1.8 million of the reports were for moderate joint pain and over 400,000 were for severe joint pain. Since v-safe only included less than 4 percent of people that received a Covid-19 vaccine, tens of millions of Americans likely had an immune reaction to the Covid-19 vaccine in their joints that resulted in debilitating pain and potential long-term harm.

There were also approximately 13,000 infants under 2 years of age who were registered for v-safe. For these 13,000 children, there were over 33,000 symptoms experienced that were significant enough to report, with the most common symptoms being irritability, sleeplessness, pain, and loss of appetite. These are very concerning since babies cannot speak and hence these symptoms are how they often communicate that something is wrong.

These data also reflect a disproportionate amount of negative health impacts, including medical events, following the Moderna vaccine versus the Pfizer vaccine. There was also a disproportionate number of negative events reported by women versus men. This is consistent with what was seen in Pfizer’s initial post-authorization safety report sent to the FDA (a report which likewise had to be obtained by lawsuit) which similarly showed a disproportionate number of neurological events experienced by women following the Pfizer Covid-19 vaccine.