Weatherman2020
Diamond Member
Deaths represented a stunning 1.3% of side effects reports.
Other than that, Mrs. Lincoln, how did you enjoy the injection?
There’s a reason the government won’t let you sue Big Pharma for damages.
While data shows that “most reported adverse events were mild and short in duration,” according to the study, which was published in the UK-based medical journal The Lancet, 6.6% of all side effects were categorized as “serious,” and resulted in “inpatient hospitalisation, prolongation of hospitalisation, permanent disability, life-threatening illness, congenital anomaly or birth defect.”
Other than that, Mrs. Lincoln, how did you enjoy the injection?
There’s a reason the government won’t let you sue Big Pharma for damages.
While data shows that “most reported adverse events were mild and short in duration,” according to the study, which was published in the UK-based medical journal The Lancet, 6.6% of all side effects were categorized as “serious,” and resulted in “inpatient hospitalisation, prolongation of hospitalisation, permanent disability, life-threatening illness, congenital anomaly or birth defect.”
Safety of mRNA vaccines administered during the initial 6 months of the US COVID-19 vaccination programme: an observational study of reports to the Vaccine Adverse Event Reporting System and v-safe
Safety data from more than 298 million doses of mRNA COVID-19 vaccine administered in the first 6 months of the US vaccination programme show that most reported adverse events were mild and short in duration.
www.thelancet.com