“A bun in the toaster oven,” a woman exclaims off-camera, handing an ultrasound image to family members who erupt into tearful emotion over the news. “Oh my God!”
The touching baby announcement video then gets down to business as text appears on the screen amidst the ongoing celebration, suggesting the best way to stay alive for this joyous birth is by becoming vaccinated against COVID-19. “Why will you get vaccinated? … Because some people you just want to meet in person.”
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The Centers for Disease Control and Prevention is pushing new COVID-19 boosters, claiming that people who don’t stay “up to date” with shots – regardless of how many they’ve already taken – “are more likely to get very sick” while those who take them annually are “much less likely to get very ill, be hospitalized, or even die” from COVID.
The Democratic nominee for president is so committed to staying up to date on jabs that Vice President Kamala Harris made COVID boosting a requirement to work on her campaign, “unless otherwise prohibited by applicable law.” They can also ask the human resources department for a “reasonable accommodation … prior to reporting to an office location.”
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A 30-year veteran of the Food and Drug Administration said at a congressional hearing this week he resigned in part because top brass sidelined his office to rush the full approval of Pfizer’s COVID-19 vaccine in August 2021, apparently to legally enable a vaccine mandate, then a booster under emergency use authorization over the objections of the agency’s outside advisers.
But former Office of Vaccines Research and Review Deputy Director Philip Krause perhaps saved his biggest embarrassment to the FDA for the end of Wednesday’s hearing on alleged Biden administration political interference in COVID vaccine review: He declined the booster.
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Kansas Attorney General Kris Kobach announced Monday that he is suing Pfizer for misleading Kansans about its COVID mRNA shots.
Kobach is accusing Pfizer of deceiving the public about the significant health risks associated with the mRNA products, and of misrepresenting the efficacy of the jabs.
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There may be a reason Pfizer chose that curious tagline in the drugmaker’s once-inescapable commercials for its COVID-19 oral antiviral – the subject of a “Saturday Night Live” parody – which cost U.S. taxpayers at least $12 billion before the feds tightened the spigot last fall and Pfizer jacked the price to $1,390 for a five-day course.
The nirmatrelvir-ritonavir combination marketed as Paxlovid does no better against so-called long COVID than a placebo taken with ritonavir, according to a new “original investigation” quietly released Friday in JAMA Internal Medicine, published by the Journal of the American Medical Association.
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The scientist who first blew the whistle on the DNA contamination in the COVID mRNA injections last year, said Monday that regulators and fact checkers have been “continually wrong” about his alarming discovery, downplaying its significance and telling flat out lies about the potential dangers.
Last April, microbiologist Kevin McKernan, published a paper establishing that simian virus 40 (SV40), a virus found in monkeys and humans, is present in Pfizer and Moderna’s mRNA COVID-19 injections. The discovery was highly significant because SV40 has been linked to cancer in humans, and since the rollout of the mRNA products, the western world has seen a dramatic increase in cancers, especially in previously healthy working aged people.
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Once she saw the data, pediatrician Dr. Renata Moon knew she had to speak out. Over her more than 20 years of practicing medicine, including more than 17 years of treating high-risk patients, Dr. Moon had never been anti-vaccine—until she saw what was happening with the COVID-19 vaccines.
In Dr. Moon’s words: “As the data rolled out on the vaccine and COVID-19, it became clear that children had basically a zero risk of death from infection by COVID [whereas] they have potential serious risk from taking the COVID-19 shots.”
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