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Open space ... not open skies what Trump defies ... 'Sapere aude'
Men with long ring fingers are less likely to die from the coronavirus: study https://t.co/NwPpEUoSfp pic.twitter.com/6jq1D85rtD— New York Post (@nypost) May 26, 2020
Men with long ring fingers are less likely to die from the coronavirus: study https://t.co/NwPpEUoSfp pic.twitter.com/6jq1D85rtD
Thomas L. Friedman, IF I DID IT (Harper Collins, 2021) pic.twitter.com/l2HbptU2Es— Gerry Canavan (@gerrycanavan) May 31, 2020
Thomas L. Friedman, IF I DID IT (Harper Collins, 2021) pic.twitter.com/l2HbptU2Es
Best knap. pic.twitter.com/Es5rUqV6yd— Kos (@Kos_) May 31, 2020
Best knap. pic.twitter.com/Es5rUqV6yd
Governments and WHO changed Covid-19 policy based on suspect data from tiny US company Diversity is the key to economic and political evolution.
In an important moment for science and data transparency, @thelancet announces that its 96,000 observational study on hydroxychloroquine has been RETRACTED. A sad story but an important one. https://t.co/qfPRsBDmP7 pic.twitter.com/GMDgP34tyb— Jeremy Faust MD MS (@jeremyfaust) June 4, 2020
In an important moment for science and data transparency, @thelancet announces that its 96,000 observational study on hydroxychloroquine has been RETRACTED. A sad story but an important one. https://t.co/qfPRsBDmP7 pic.twitter.com/GMDgP34tyb
< wipes tears >
The price of the drug in the region is not yet known. In the United States, it could be priced up to $5,080 (4,532) per course, while Indian generic drugmakers will sell the treatment between 5,000 rupees to 6,000 rupees (59-71). The EMA endorsement, which comes just weeks after a speedy review, means physicians can prescribe the Gilead drug, to be branded Veklury, in Europe once approved by the European Commission, which usually follows CHMP recommendations.
The EMA endorsement, which comes just weeks after a speedy review, means physicians can prescribe the Gilead drug, to be branded Veklury, in Europe once approved by the European Commission, which usually follows CHMP recommendations.
Drugmaker Gilead sets its price for the Covid-19 treatment remdesivir as HHS secures doses https://t.co/Eu9napRDAq— POLITICO (@politico) June 29, 2020
Drugmaker Gilead sets its price for the Covid-19 treatment remdesivir as HHS secures doses https://t.co/Eu9napRDAq
As Gilead charges $3,120 for its COVID drug, remdesivir, remember that the drug was developed with a $70,000,000 grant from the federal government paid for by American taxpayers.Once again, Big Pharma is set to profit on the people's dime.— Robert Reich (@RBReich) June 29, 2020
As Gilead charges $3,120 for its COVID drug, remdesivir, remember that the drug was developed with a $70,000,000 grant from the federal government paid for by American taxpayers.Once again, Big Pharma is set to profit on the people's dime.
The $2,300 price of a course of remdesivir may sound high - and is compared with the basic cost of manufacturing the stuff - but is actually fairly restrained. ...
Ahead of November's presidential election, the $94 billion pharma group's restraint may help it accumulate political capital.
The U.S. has bought nearly the entire global [!] supply of the antiviral drug remdesivir, the only treatment licensed to treat COVID-19, as the nation continues to experience surging cases of coronavirus. [...] The Trump administration announced this week the U.S. struck an agreement with Gilead to secure more than 500,000 treatment courses of the drug for American hospitals [!] through September. [...] Ohid Yaqub, a senior lecturer at the University of Sussex, called it disappointing news. "It so clearly signals an unwillingness to cooperate with other countries and the chilling effect this has on international agreements about intellectual property rights," Yaqub said, according to the Associated Press [!].
"It so clearly signals an unwillingness to cooperate with other countries and the chilling effect this has on international agreements about intellectual property rights," Yaqub said, according to the Associated Press [!].
[Andrew Hill, senior visiting research fellow at Liverpool University] told The Guardian that the UK could get access to remdesivir through a compulsory license, which overrides the intellectual property rights of the company. This would allow the UK to purchase from generic companies in Bangladesh or India where Gilead's patent is not recognized.
In the developing world, where healthcare resources, infrastructure and economics are so different, we have entered into agreements with generic manufacturers to deliver treatment at a substantially lower cost.
Setting The Henry Ford Health System (HFHS) in Southeast Michigan: large six hospital integrated health system; the largest of hospitals is an 802-bed quaternary academic teaching hospital in urban Detroit, Michigan. Participants Consecutive patients hospitalized with a COVID-related admission in the health system from March 10,2020 to May 2,2020 were included. Only the first admission was included for patients with multiple admissions. All patients evaluated were 18 years of age and older and were treated as inpatients for at least 48 hours unless expired within 24 hours. Exposure Receipt of hydroxychloroquine alone, hydroxychloroquine in combination with azithromycin, azithromycin alone, or neither. Main Outcome The primary outcome was in-hospital mortality. Results Of 2,541 patients, with a median total hospitalization time of 6 days (IQR: 4-10 days), median age was 64 years (IQR:53-76 years), 51% male, 56% African American, with median time to follow-up of 28.5 days (IQR:3-53). Overall in-hospital mortality was 18.1% (95% CI:16.6%-19.7%); by treatment: hydroxychloroquine + azithromycin, 157/783 (20.1% [95% CI: 17.3%-23.0%]), hydroxychloroquine alone, 162/1202 (13.5% [95% CI: 11.6%-15.5%]), azithromycin alone, 33/147 (22.4% [95% CI: 16.0%-30.1%]), and neither drug, 108/409 (26.4% [95% CI: 22.2%-31.0%]). Primary cause of mortality was respiratory failure (88%); [...] Primary cause of mortality in the 460 patients was: 88% respiratory failure, 4% cardiac arrest (with mean QTc interval from last ECG reading 471 ms), 8% other cardiopulmonary arrest and multi-organ failure. No patient had documented torsades de pointes. ...
Participants Consecutive patients hospitalized with a COVID-related admission in the health system from March 10,2020 to May 2,2020 were included. Only the first admission was included for patients with multiple admissions. All patients evaluated were 18 years of age and older and were treated as inpatients for at least 48 hours unless expired within 24 hours.
Exposure Receipt of hydroxychloroquine alone, hydroxychloroquine in combination with azithromycin, azithromycin alone, or neither.
Main Outcome The primary outcome was in-hospital mortality.
Results Of 2,541 patients, with a median total hospitalization time of 6 days (IQR: 4-10 days), median age was 64 years (IQR:53-76 years), 51% male, 56% African American, with median time to follow-up of 28.5 days (IQR:3-53). Overall in-hospital mortality was 18.1% (95% CI:16.6%-19.7%); by treatment: hydroxychloroquine + azithromycin, 157/783 (20.1% [95% CI: 17.3%-23.0%]), hydroxychloroquine alone, 162/1202 (13.5% [95% CI: 11.6%-15.5%]), azithromycin alone, 33/147 (22.4% [95% CI: 16.0%-30.1%]), and neither drug, 108/409 (26.4% [95% CI: 22.2%-31.0%]). Primary cause of mortality was respiratory failure (88%); [...] Primary cause of mortality in the 460 patients was: 88% respiratory failure, 4% cardiac arrest (with mean QTc interval from last ECG reading 471 ms), 8% other cardiopulmonary arrest and multi-organ failure. No patient had documented torsades de pointes. ...
The Florida Department of Law Enforcement detailed the last two weeks of Carsyn's life in a public Medical Examiner's report.
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