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Likes: lies post the damn articleOriginally Posted by bsm2
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lies post the damn article
... the point is this a global conference with no masking and no proof of vaccination in a state that is a COVID denier because of politics.
How people can be so stupid as to not take basic precautions is a perfect incubator for COVID.
,,, why bother? Hydroxycloroquine is never going to be approved by the FDA as a COVID treatment. Time to grow up and move on.
lies post the damn article
Hydroxychloroquine is effective, and consistently so when provided early, for COVID-19: a systematic review - PubMed
BULLETIN—NIH Clinical Trial Evaluating Hydroxychloroquine and Azithromycin for COVID-19 Closes Early | NIH: National Institute of Allergy and Infectious Diseases
both of these reports from NIH/NIAID says it is effective...
more bullshit lies from the bullshitmaster
I took all the precautions needed when I got vaccinated. I'm wide open.
get your head out of you ass I posted TWO reports from the NIH/NIAID saying that it DOES WORK.
fuck off little man you are outta your league
Your Posts get more Riduilous by the day.
Try Google next time
Game Over
Facts Vs Fiction
Re: Latest on the Corona Virus
A National Institutes of Health clinical trial evaluating the safety and effectiveness of hydroxychloroquine for the treatment of adults with coronavirus disease 2019 (COVID-19) has formally concluded that the drug provides no clinical benefit to hospitalized patients.
Wow!!! You lie while calling others liars. Funny shit.
The first article states, "We hypothesized that a systematic review would show HCQ to be effective against COVID-19".
A hypothesis is not a statement of effectiveness.
The second article doesn't even make any kind of a statement about effectiveness. It say the study was closed because there weren't enough participants.
What else ya got???
[QUOTE=copier addict;1798908]Wow!!! You lie while calling others liars. Funny shit.
The first article states, "We hypothesized that a systematic review would show HCQ to be effective against COVID-19".
A hypothesis is not a statement of effectiveness.
The second article doesn't even make any kind of a statement about effectiveness. It say the study was closed because there weren't enough participants.
What else ya got???[/
I listened to 4 different stations on radio yesterday and one of them is a left wing dem station and all of them reported the same story how the study shows it is effective. The only difference is that on the dem station when they came out of the news the hosts said nothing about the story,I am sure because they would be embarased to.
WOW I feel so much more comfortable about the shot now! NOT!
FDA Finds 60 Million COVID Vaccine Doses Were Potentially Contaminated: Report
The Food and Drug Administration told Johnson & Johnson that about 60 million doses of its COVID-19 vaccine made at a Baltimore plant cannot be used, according to a new report.
The New York Times was the first to report on Friday, “The Food and Drug Administration plans to allow about 10 million doses to be distributed in the United States or sent to other countries, but with a warning that regulators cannot guarantee that Emergent BioSolutions, the company that operates the plant, followed good manufacturing practices.”
The report added, “The agency has not yet decided whether Emergent can reopen the factory, which has been closed for two months because of regulatory concerns.”
“More than 100 million doses of Johnson & Johnson and at least 70 million doses of AstraZeneca were put on hold after Emergent discovered in March that its workers had contaminated a batch of Johnson & Johnson’s vaccine with a key ingredient used to produce AstraZeneca’s. Federal officials then ordered the plant to pause production, stripped Emergent of its responsibility to produce AstraZeneca’s vaccine and instructed Johnson & Johnson to assert direct control over the manufacturing of its vaccine there.”
In a statement, the FDA said, “Before making this decision, the FDA conducted a thorough review of facility records and the results of quality testing performed by the manufacturer. Based on this review and considering the current COVID-19 public health emergency, the FDA concluded these batches are suitable for use.
“While the FDA is not yet ready to include the Emergent BioSolutions plant in the Janssen EUA as an authorized manufacturing facility, the agency continues to work through issues there with Janssen and Emergent BioSolutions management.”
Politico, meanwhile, reported, “FDA ordered Emergent to stop producing vaccines for Johnson & Johnson and AstraZeneca in March after Emergent inadvertently contaminated 15 million J&J shots with the active ingredient from the AstraZeneca vaccine.”
It added, “Tens of millions of doses of each company’s vaccine have been in limbo while federal regulators tested them to rule out contamination and determine if they are safe to use.”
Emergent BioSolutions is a Maryland-based contractor for Johnson & Johnson.
Emergent is a government-endorsed supplier of a COVID-19 vaccine.
The Hill reported, “The loss of 60 million doses is the latest setback for Emergent. The plant, which has been under scrutiny for months, was shuttered in April for a host of violations, including contamination of Johnson & Johnson’s vaccine with an ingredient for the AstraZeneca vaccine, which were both being manufactured by Emergent at the time.”
The report added, “The federal government has paid Emergent more than $271 million in taxpayer money, but the ensuing delays have meant that none of the millions of doses of the J&J vaccine produced at the plant have been distributed.”
In March, reports claimed the Biden administration knew about a contaminated coronavirus vaccine batch that forced 15 million doses to be trashed but hid the debacle from the public.
In April, the Centers for Disease Control paused the Johnson & Johnson vaccine’s rollout after reports of severe blood clots appeared in a handful of women across the United States.
Just a few dozen cases were reported among the approximately 9 million doses administered, NBC News reported in May, citing the CDC.
The CDC lifted the pause shortly afterward. The vaccine is now accompanied by a warning label that notes the extremely slim possibility of developing a serious blood clot after receiving it.
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