https://pjmedia.com/news-and-politics/benbartee/2023/09/06/why-is-the-cdc-no-longer-collecting-adverse-events-reports-for-covid-19-shots-n1724876
For reasons unexplained, the CDC recently ceased its collection of adverse events reports via its “V-safe” reporting system regarding the COVID-19 mRNA injections deceptively marketed as “vaccines.”
Via Brownstone Institute (emphasis added):
The Centers for Disease Control and Prevention (CDC) V-safe website quietly stopped collecting adverse event reports with no reason or explanation…
VAERS and V-safe are mutually exclusive safety collection databases operated by the FDA and CDC, respectively. VAERS is an older way of collecting safety data where one can fill out a form online, or manually, or by calling a toll-free number, whereas V-safe is a device “app” which requires online registration. Both VAERS and V-safe collect personal information, lot numbers, dates and associated information, but V-safe was an active collection system geared towards a younger app-using demographic.
Here is what the V-safe website reads as of September 2:
Thank you for your participation.
Data collection for COVID-19 vaccines concluded on June 30, 2023.
If you have symptoms or health problems following your COVID-19 vaccination that concern you, please contact your healthcare provider.
You can also report to the Vaccine Adverse Event Reporting System (VAERS).
VAERS, as I have documented previously elsewhere, is notoriously unreliable as a gauge of the actual rate of adverse events. As few as 1% of adverse events from injections are reported to the system. There are several potential reasons for this deficiency:
It is a voluntary reporting system, so healthcare providers are not ethically or legally required to report incidents of adverse events among their patients. You can imagine, as many doctors/nurses work within large medical systems intertwined with the insurance and pharmaceutical industries, what kind of institutional disincentives might exist to discourage their use of VAERS.
There is no governmental oversight of complaints levied by patients to doctors and/or pharmaceutical companies to ensure that verbal patient reports ever make it into the system.
Like any government program, the VAERS system is a labyrinthine clusterf*** of bureaucratic rigmarole, and navigating it as a layperson is difficult — particularly for a patient or his/her family already distressed by a vaccine injury.
Studies have shown that, in fact, many healthcare providers themselves don’t know how to file a VAERS report.