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European Medicines Agency gives green light for Pfizer's anti-Covid pill "in case of emergency"

2021-12-16T17:28:30.043Z


This approval should enable countries wishing for early use to be able to treat the most fragile adults from the outset.


It is a treatment that is eagerly awaited by those most at risk of a coronavirus infection.

On Thursday, the European Medicines Agency (EMA) announced that it had approved the use, in an emergency, in the European Union, of the anti-Covid pill from Pfizer, which has not yet received an authorization complete marketing.

“The drug, which is not yet authorized in the EU, can be used to treat adults with Covid-19 who do not need supplemental oxygen and who are at increased risk of developing a severe form of disease, ”the EMA said in a statement.

Read alsoAn agreement signed to facilitate global access to Pfizer's anti-Covid pill

"The EMA has issued this opinion to support national authorities who can decide on a possible early use of the drug" as the continent faces an outbreak of the epidemic.

The pharmaceutical giant announced earlier this week that its anti-Covid pill reduced hospitalizations and deaths in people at risk by almost 90% when taken in the first days after symptoms appeared.

The latter, named Paxlovid, should remain effective against Omicron according to laboratory tests, Pfizer also announced.

The EMA recommendation is based on interim results from the main study in outpatients and unvaccinated patients with symptomatic disease who were at risk of developing a severe form of the disease.

Pending marketing authorization

These results indicate that Paxlovid "reduced the risk of hospitalization and death when treatment was given within 5 days of onset of symptoms," and treatment should be extended over five days.

Antivirals work by reducing the ability of a virus to replicate, thereby slowing down the disease.

They are eagerly awaited because they are easy to administer and can be taken at home with a glass of water.

Treatment is not recommended during pregnancy and in people who may become pregnant.

Breast-feeding should also be discontinued while taking treatment.

The most common side effects were taste disturbance, diarrhea and nausea.

Read alsoThe United States orders Pfizer 10 million treatments of its anti-Covid pill

The EMA also launched an expedited treatment review on December 13, 2021 for a possible marketing authorization application, which could take place in several weeks.

The EMA had previously issued a similar emergency use authorization for a pill from Pfizer's rival, Merck.

The pandemic has killed at least 5,328,762 people worldwide since the end of 2019, according to a report established by AFP from official sources, Thursday at 11 a.m.

The United States is the most bereaved country with 802,511 deaths, ahead of Brazil (617,271), India (476,478) and Mexico (297,187).

The WHO estimates, taking into account the excess mortality directly and indirectly linked to Covid-19, that the toll of the pandemic in the world could be two to three times higher.

Source: leparis

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