CDC Director Admits Agency Gave False Information on COVID-19 Vaccine Safety Monitoring

What is and has been the CDC hiding?

Many people who took the Johnson and Johnson vaccine for the prevention of Covid-19 complained of severe headaches in the aftermath. J&J denied this claim vehemently. Later, the same vaccinated people contracted the virus. The question is did the CDC do its due diligence prior to approving the J&J vaccine for public use?

Pfizer had a similar problem with its Covid-19 vaccine. Among all vaccine recipients, 66.6% reported at least one systemic reaction in the 7 days after vaccination. The frequency and severity of systemic adverse events was higher after dose 2 than dose 1. Fatigue, headache, chills, and new or worsened muscle pain were most common. The majority of systemic events were mild or moderate in severity, after both doses. Fever was more common after the second dose than after the first dose. Overall, the median onset of systemic adverse events in the vaccine group in general was 1 to 4 days after either dose and lasted a median duration of 1 day. One grade 4 fever (>40.0°C) was reported in the vaccine group. No other systemic grade 4 reactions were reported.

Moderna vaccine for Covid-19 caused level 3 and level 4 systemic reactions.

Why did the CDC and FDA approve such vaccines for emergency use, when there were severe reactions after being administered the first dose and/or the second dose; did these vaccines actually prevent the spread of Covid-19 in the U.S.? Kindly share your thoughts on this topic.