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President Donald Trump predicted on Friday that the US would have enough coronavirus vaccines for anyone who wanted one to have one by April 2021.Trump’s timeline is a bit sped up compared to timeframes offered by several government experts, including CDC Director Robert Redfield and Dr. Anthony Fauci, director of the National Institute of Allergy and Infectious Diseases. Fauci and Redfield have suggested the a potential coronavirus vaccine would be widely available by the middle of 2021.Trump said that the US would begin distributing vaccines within 24 hours of FDA approval of a vaccine, which he has suggested could happen as soon as the end of October.“We will have manufactured at least 100 million vaccine doses before the end of the year,” Trump said. “And likely much more than that. Hundreds of millions of doses will be available every month and we expect to have enough vaccines for every American by April. Again, I will say even at that later stage, delivery will go as fast as it comes, they can deliver.”Dr. Scott Atlas, a neurosurgeon who recently joined the White House coronavirus task force, agreed with Trump’s timeline. The highest risk Americans could expect to be vaccinated by January.“The people on the prioritized lists, including high risk and first responders will have the ability to take the vaccine. At the latest, in January,” Atlas said.“There will be hundreds of millions of doses delivered for people to take it during the first quarter [of 2021] and so that by April, every single American who wants to be vaccinated will have the ability to be vaccinated. It is not a forced vaccination,” Atlas added.Redfield said it might not be until the middle of 2021 before a vaccine is widely available."I think we're probably looking at third late second quarter, third quarter 2021,” he said on Wednesday.Trump later said that Redfield was “confused” over the timing of a vaccine."I think he made a mistake when he said that,” Trump said. “That's just incorrect information. I called him and he didn't tell me that and I think he got the message maybe confused. maybe it was stated incorrectly.”Trump said on Friday that he thinks the timeline given by Redfield and Fauci can be shortened “considerably.”There are several vaccines in Phase 3 testing. Even though a vaccine could be approved by year’s end, trials will be expected to continue for over a year to monitor for possible side effects.According to the FDA, a typical Phase 3 trial would take one to three years. 2514

POWAY, Calif. (KGTV) - The Poway Unified School District sent parents an email over the weekend on their action plan after a water boil advisory was issued."My boys and I have had the discussion of the importance of safety," Mother and Senior Management Analyst of Poway Public Works Jessica Parks said of her twin high schoolers. "The rule of thumb is don't get the water in your mouth."The City of Poway issued a precautionary boil water advisory Saturday.The city says it believes the recent storm possibly compromised the potable drinking water system.As a precaution, the city is advising resident to boil tap water or use bottled water for drinking or cooking until further notice."I am really pleased with the Poway Unified School District for getting that message out there, speaking to all the parents and letting them know safety for their children is number one," Parks said.Poway Unified School District sent this email to parents: 951

Potential accuracy issues with a widely used coronavirus test could lead to false results for patients, U.S. health officials warned.The Food and Drug Administration issued the alert Monday to doctors and laboratory technicians using Thermo Fisher’s TaqPath genetic test. Regulators said issues related to laboratory equipment and software used to run the test could lead to inaccuracies. The agency advised technicians to follow updated instructions and software developed by the company to ensure accurate results.The warning comes nearly a month after Connecticut public health officials first reported that at least 90 people had received false positive results for the coronavirus. Most of those receiving the false results were residents of nursing homes or assisted living facilities.A spokeswoman for Thermo Fisher said the company was working with FDA “to make sure that laboratory personnel understand the need for strict adherence to the instructions for use.” She added that company data shows most users “follow our workflow properly and obtain accurate results.”The FDA said one possible problem was related to the incorrect use of equipment that rapidly spins samples in preparation for processing. The agency’s letter tells lab workers to follow new instructions developed by the company for this step.A second issue relates to the software used on Thermo Fisher’s testing platform. FDA said labs must upgrade the software to a new version.Dr. Albert Ko of Yale’s School of Public Health said the potential accuracy problems have “pretty serious implications” given that Thermo Fisher’s test is used widely both in the U.S. and around the world to screen for coronavirus.The FDA statement did not provide any details on how many test results may have been affected by the problem.Lab tests are the backbone of U.S. screening for coronavirus, accounting for more than half of the roughly 750,000 tests developed daily. The tests look for traces of coronavirus’ genetic material in nasal swabs taken from patients.Thermo Fisher’s test was granted emergency use by the FDA in mid-March. The test runs on a large, automated machine used in hospital, government and commercial labs to look for diseases such as HIV, hepatitis and flu.The FDA has used its emergency powers to OK more than 200 tests for coronavirus since February. No test is perfect and all are expected to give at least a small percentage of false negatives and false positives.___The Associated Press Health and Science Department receives support from the Howard Hughes Medical Institute’s Department of Science Education. The AP is solely responsible for all content. 2656

PORTLAND, Ore. (AP) — Police in Portland, Oregon, declared a riot as protesters demonstrated outside a law enforcement building early Sunday, continuing a nightly ritual in the city. Officers used crowd-control munitions including smoke to disperse the gathering outside the Penumbra Kelly building. Police said protesters had thrown "softball size" rocks, glass bottles and other objects at officers. Police also reported vandalism at the building. The actions came after what started as a peaceful protest late Saturday. Violence had erupted earlier Saturday afternoon when a small group of far-right demonstrators traded paintballs and pepper spray with counter-protesters. 684

Prescription drug ads are on every channel, and with them come the laundry list of side effects tacked on at the end of every TV spot. Now, in addition to listing those side effects, you could soon be hearing about the costs.A new proposal from the Trump administration would force manufacturers to state a drug's list price in any TV advertisement.It was a goal first laid out by Human and Health Services Secretary Alex Azar back in May."If we wanna have a real market for drugs, why not have them disclose their prices in the ads too?” asked Azar. “Consumers would have more balanced info and companies would have incentives for setting their prices…"Experts on drug pricing, like John Hopkins University's Gerard Anderson, say it’s about time."If you’re buying a TV, they'll tell you what a TV costs. If the grocery store’s having a sale, they’ll say how much oranges cost. This is something that should be and is just long overdue in the pharma industry,” Anderson says.Pharmaceutical companies have pushed back via their trade group, which said that posting prices on TV could be "misleading or confusing.” Their proposal was to, instead, tell consumers that pricing information could be found on the drug's website."The problem is that most of us would never go to their website to look up that information,” Anderson explains. “And the FDA would have to monitor closely the info on their site and that could change daily. So, it’s really not a viable option."The proposal will be open for public comment for 60 days, and even if it goes into effect after that, industry experts say they're likely to face many legal challenges from the pharmaceutical industry. 1676

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