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News & Articles By Ramon Tomey
03/08/2023
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By Ramon Tomey
FDA announces voluntary recall of contaminated eye drops that could blind people
The Food and Drug Administration (FDA) has announced the voluntary recall of contaminated eye drops that could cause bacterial infection and eventual blindness with continued use. According to a March 3 announcement by the regulator, the Phoenix-based Pharmedica is recalling two lots of its Purely Soothing 15 Percent MSM Drops due to “non-sterility” issues. It […]
03/07/2023
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By Ramon Tomey
FDA rejects Elon Musk’s bid to test Neuralink brain implants in humans
The Food and Drug Administration (FDA) has rejected Elon Musk’s application to conduct human trials of his Neuralink brain implant device over safety concerns. Seven current and former employees confirmed the FDA’s decision to Reuters. The regulator outlined dozens of issues the company must address before proceeding to human trials. These issues involved the device’s […]
11/23/2022
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By Ramon Tomey
GSK halts US sales of its blood cancer drug Blenrep
British pharmaceutical firm GSK announced that it will stop selling its blood cancer drug Blenrep in the United States. The company announced on Nov. 22 that it has begun the process to withdraw the drug’s marketing authorization in the country. It clarified, however, that trials for the drug would continue and that some patients would […]
11/17/2022
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By Ramon Tomey
FDA declares lab-grown meat from UPSIDE Foods safe for human consumption – but is it?
The Food and Drug Administration (FDA) recently declared lab-grown meat from a California-based company safe for human consumption. In a Nov. 16 press release, the regulator announced that it has granted artificial chicken products from Berkeley, California-based UPSIDE Foods the “generally recognized as safe” (GRAS) designation. Formerly known as Memphis Meats, UPSIDE Foods makes cell-cultured chicken fillets […]
11/13/2022
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By Ramon Tomey
AstraZeneca drops plan to seek US approval for its COVID-19 vaccine
Anglo-Swedish vaccine maker AstraZeneca announced that it will no longer pursue emergency approval for its Wuhan coronavirus (COVID-19) vaccine in the United States. Early on in the pandemic, the manufacturer applied for an emergency use authorization (EUA) with the U.S. Food and Drug Administration (FDA). However, the regulator refused to authorize the shot after its […]
10/26/2022
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By Ramon Tomey
Pfizer’s Paxlovid antiviral drug for COVID-19 linked to blood clots
Pfizer’s Paxlovid antiviral medication, which is meant to treat Wuhan coronavirus (COVID-19) infections, has been linked to cases of blood clots. The Food and Drug Administration (FDA) first authorized Paxlovid, a combination of the two antiviral medications nirmatrelvir and ritonavir in December 2021. But these two drugs have significant risks of their own, with ritonavir […]
10/18/2022
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By Ramon Tomey
GMO ingredients in “fake meat” Impossible Burgers linked to health issues
The globalists have promoted fake meat as a “healthy” and “environmentally friendly” alternative to the real thing. However, two ingredients in these meat analogues are reportedly linked to weight gain and kidney disease, making fake meat products far from healthy. Health freedom group Children’s Health Defense (CHD) reported on the matter, citing a study done […]
10/17/2022
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By Ramon Tomey
Dr. Paul Offit admits new COVID bivalent boosters offer NO BENEFITS
Dr. Paul Offit, one of the Food and Drug Administration‘s (FDA) vaccine advisers, admitted on video that the new Wuhan coronavirus (COVID-19) bivalent boosters have no benefits whatsoever. Vaccine safety advocate Steve Kirsch posted a video of Offit’s remarks about the boosters during the expert’s interview with CNBC. Offit, a member of the FDA’s Vaccines […]
09/27/2022
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By Ramon Tomey
FDA vaccine adviser warns young people against getting COVID bivalent booster
An adviser to the Food and Drug Administration (FDA) warned young people against getting the latest version of the Wuhan coronavirus (COVID-19) booster doses. Dr. Paul Offit, a member of the FDA’s Vaccines and Related Biological Products Advisory Committee (VRBPAC), expressed doubts over the COVID-19 bivalent booster. The regulator reportedly approved the updated version of […]
08/05/2022
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By Ramon Tomey
After years of denial, European Medicines Agency now confirms Novavax COVID shot causes cardiac inflammation
The European Union’s regulator for vaccines has confirmed that the Wuhan coronavirus (COVID-19) vaccine made by Novavax can cause cardiac inflammation. The European Medicines Agency (EMA) said on Aug. 3 that the Maryland-based drug firm’s Nuvaxovid vaccine should list myocarditis (heart muscle inflammation) and pericarditis (heart lining inflammation) as potential side effects. It has asked Novavax […]
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