V-safe data release
Just a slide...
The Informed Consent Network (ICAN) teamed with Aaron Siri’s team have successfully sued for release of v-safe data to the public. You can learn more about that here. This data set is described as the following:
The [v-safe] initiative was created for the covid-19 vaccines to complement the Centers for Disease Control and Prevention’s vaccine safety monitoring system. Known as v-safe, the registry lets inoculated people report their experiences, including serious suspected side effects, directly to the CDC through smartphones, adding to the data gathered from clinical trials and other safety monitoring systems.1
Check this out. And follow the CDC’s orders peasant! GET VACCINATED YOU IDIOT! GET A SMARTPHONE YOU IDIOT! GET SAFE YOU IDIOT!
There’s only one thing I wanted to share about my observation of the ICAN v-safe Dashboard, and that is the following slide. Unfortunately, the v-safe data set, albeit it a huge list of people who entered data, is lacking in adverse events - both in types and filed input. They allow a measly 18 adverse events2 to be reported by users as opposed to the over 25,000 MedDRA PT codes (25,592 to be precise) used in the VAERS context of which over 14,000 have been reported in the context of the COVID-19 injections. I haven’t used v-safe, but I imagine the app uses a pull-down menu of adverse events leaving essentially 25,574 adverse event types unavailable for use. And just to be a bit facetious, as per Pfizer’s own list of adverse events of special interest that lists 1291 adverse events, this leaves 1,273 adverse event types unavailable for use.
This screenshot shows that ~8% of the v-safe users who checked-in due to experiencing an ‘impact’ required medical care.
That’s not a small percentage.
https://khn.org/news/article/v-safe-how-everyday-people-help-the-cdc-track-covid-vaccine-safety-with-their-phones/
ABDOMINAL PAIN, CHILLS, DIARRHEA, FATIGUE, GROIN UNDERARM SWELLING, HEADACHE, IRRITABILITY, ITCHING, JOINT PAINS, LOSS OF APPETITE, MUSCLE OR BODY ACHES, NAUSEA, PAIN, RASH OUTSIDE INJECTION SITE, REDNESS, SLEEPINESS, SWELLING, VOMITING
I didn’t see myocarditis in that list, nor facial paralysis, tremors, difficulty walking or standing, irregular heartbeat, racing heart, changes in blood pressure, blood clots, tinnitus, breakthrough infection, new onset diabetes, new onset cancer, etc. on that list....
33% of people suffered an adverse event and did a report on vsafe. This can be used to calculate the VAERS underreporting factor. 124 (I said originally 140, corrected it)
And they are still suing to get the data from the accompanying text-field, which was NOT released. I presume the text field was where they said things like, “I have myocarditis! What did you do to me!” Etc