USA. U. S. Makes COVID Antiviral Drug More Available at Test sites

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A lab technician at a Pfizer plant inspects the production process of Paxlovid tablets. (Pfizer)

The first effects of in-depth research on the long COVID have produced provocative effects. Researchers do not perceive the persistent symptoms of the mechanism.

Pfizer plans to present the new data to the Food and Drug Administration this week, bringing families with young children closer to a long-awaited vaccine.

As the summer months approach, Jha said the “first” thing other people want to do is “get stronger,” and if they have an advanced infection, they see their doctor for Paxlovid. He said meetings of all sizes can take a stand. safer thanks to the available equipment, if other people use it.

“In places in the country where recovery rates are much lower, where the infection will spread more, I’m sure we’re going to see, unfortunately, more serious illness,” he said.

“Being vaccinated and strengthened is a vital component in ensuring that such activities are particularly safer,” he added. If you get an advanced infection, you are still protected from serious diseases. “

USA. The U. S. food and drug administration ordered 20 million Paxlovid cures from drugmaker Pfizer, and the country will most likely run out of this drug this winter if the drug continues to be widely used. plus Paxlovid and other treatments, as well as other boosters.

While management has begun making plans for the possible desire to ration the federal vaccine source if Congress does not act, Jha said at this time that his message to prescribers is that they care about the source.

“I think we now use whatever is mandatory to protect Americans,” Jha said.

Listen anytime, anywhere.

If the CDC as planned, it would open a third COVID-19 vaccine for healthy children of age number one, as is already advised for everyone over the age of 12.

The growing number of COVID-19 infections and hospitalizations is subjecting more of the country to rules issued through the CDC that require the use of masks and precautions.

Tuesday’s Food and Drug Administration action now opens a third blow also for elementary-age children, at least months after their last dose.

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