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Too Many Adverse Reactions: CA Temporarily Stops Injections Of Moderna’s COVID Vaccine

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Published on: January 19, 2021

California has apparently halted the mass injections of Moderna’s COVID-19 vaccine batch due to a “higher-than-usual number of adverse events.”  People’s bodies are not responding well to these new vaccines. And don’t forget, the vaccine manufacture has immunity when someone is injured or killed by these vaccines.

Big Pharma Will Not Be Responsible For COVID-19 Side Effects Caused By Vaccines

According to a report by RT, state epidemiologist Dr. Erica S. Pan said in a statement that “fewer than 10 individuals” suffered “a possible severe allergic reaction” and required medical attention over the past 24 hours after being injected with the specific batch of vaccine. All of the incidents appear to have occurred at a single community clinic that was administering the lot. The vaccine site was reportedly closed for several hours after the string of adverse reactions occurred, before switching to a different batch of the same vaccine.

“Out of an extreme abundance of caution and also recognizing the extremely limited supply of vaccine, we are recommending that providers use other available vaccine inventory,” the health official said.

Big Pharma, the government, and health care “authorities” want everyone to know that severe adverse reactions to vaccines are “rare.” But have no fear, the government will go ahead and review these incidents, so you can be told the propagandized “truth” and line up for this jab.

Moderna, the Centers for Disease Control and Prevention (CDC), and the US Food and Drug Administration (FDA) are reviewing the batch and all relevant medical data.

The Covid-19 jab has been linked to other cases of serious medical emergencies. In December, a physician in Boston said he suffered one of the worst allergic reactions he’s ever experienced after receiving Moderna’s vaccine, describing the episode as potentially life-threatening.

Similar cases linked to the Pfizer/BioNTech vaccine have been referred to the CDC and FDA for review. –RT

Article posted with permission from Mac Slavo

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