Advances in the fight against the coronavirus

[GuyGadeboisTheBack]

They are formidable, they are defended here even by: Izy, Bouzo and Végaz, the trio of gnomes (You see, Kiki, I did not include you in the top 3 ...):

Paxlovid: Pfizer's anti-Covid pill coming soon? What efficiency?

ANTI-COVID PILL. On November 16, Pfizer launched an emergency authorization request from the United States Medicines Agency (FDA) for its anti-Covid pill, Paxlovid.

[Updated November 18, 2021, 16:21 pm] This Tuesday, November 16, Pfizer announced that it had launched an emergency authorization request from the US Medicines Agency for its Paxlovid, a pill to be ingested preventing Covid-19 from replicate in the organism. The firm also said on the same day that it had signed a voluntary licensing agreement with the Medicines Patent Pool, which would allow sub-licenses to produce generic drugs and supply up to 95 countries around the world. On the other hand, it will be necessary to wait for the European Medicines Agency to give its approval for marketing in France.

On November 5, the American laboratory revealed in a press release that it had stopped clinical trials of its drug which, associated with another antiviral, reduces the risk of severe forms by 89%, according to the first results. The purpose of this suspension was to speed up the application for marketing authorization for the drug in the United States. Indeed, the pharmaceutical company had indicated that it wanted to send the provisional data resulting from the first tests as soon as possible to the Food and Drug Administration, the American drug agency. Encouraging results which are timely, after the recent PfizerGate.

https://www.linternaute.com/actualite/g ... fficacite/

[Janic]

and long live the new BP miracle!

[Christophe]

They are formidable, they are defended here even by: Izy, Bouzo and Végaz, the trio of gnomes (You see, Kiki, I did not include you in the top 3 ...):

Paxlovid: Pfizer's anti-Covid pill coming soon? What efficiency?

ANTI-COVID PILL. On November 16, Pfizer launched an emergency authorization request from the United States Medicines Agency (FDA) for its anti-Covid pill, Paxlovid.

[Updated November 18, 2021, 16:21 pm] This Tuesday, November 16, Pfizer announced that it had launched an emergency authorization request from the US Medicines Agency for its Paxlovid, a pill to be ingested preventing Covid-19 from replicate in the organism. The firm also said on the same day that it had signed a voluntary licensing agreement with the Medicines Patent Pool, which would allow sub-licenses to produce generic drugs and supply up to 95 countries around the world. On the other hand, it will be necessary to wait for the European Medicines Agency to give its approval for marketing in France.

On November 5, the American laboratory revealed in a press release that it had stopped clinical trials of its drug which, associated with another antiviral, reduces the risk of severe forms by 89%, according to the first results. The purpose of this suspension was to speed up the application for marketing authorization for the drug in the United States. Indeed, the pharmaceutical company had indicated that it wanted to send the provisional data resulting from the first tests as soon as possible to the Food and Drug Administration, the American drug agency. Encouraging results which are timely, after the recent PfizerGate.

https://www.linternaute.com/actualite/g ... fficacite/

They got their name wrong !!

PAXCOVID would have sounded better! At least for all languages ​​of Latin origin

Bunch of morons of overpaid executives!

ps: my mom taught me that when you got ripped off once by a person *, you don't have to trust her the second time ... society-and-philosophy / human-societies-everything-is-trusted-t11776.html

* physical at the time but I add moral today

[Obamot]

associated with another antiviral, reduces the risk of severe forms by 89%,

Ah, from the outset it was announced below the 95% efficiency of machinery-vaccines from the same dairy ...

It begins badly...!

[GuyGadeboisTheBack]

ps: my mom taught me that when you got ripped off once by a person *, you don't have to trust her the second time ...

[Janic]

associated with another antiviral, reduces the risk of severe forms by 89%,

everything is bogus in these statements, once again. Most of the high-risk victims either died or got away with it, not because of the vaccine, but despite the vaccine as since Pasteur! Therefore, the remaining patients have less risk of developing severe forms. Let's not confuse the immune system reacting to the wild virus and the immune system reacting to the pseudo-vaccine cobbled together by the labs. Cabbages are not carrots!

[Adrien (ex-nico239)]

They are formidable, they are defended here even by: Izy, Bouzo and Végaz, the trio of gnomes (You see, Kiki, I did not include you in the top 3 ...):

Paxlovid: Pfizer's anti-Covid pill coming soon? What efficiency?

ANTI-COVID PILL. On November 16, Pfizer launched an emergency authorization request from the United States Medicines Agency (FDA) for its anti-Covid pill, Paxlovid.

[Updated November 18, 2021, 16:21 pm] This Tuesday, November 16, Pfizer announced that it had launched an emergency authorization request from the US Medicines Agency for its Paxlovid, a pill to be ingested preventing Covid-19 from replicate in the organism. The firm also said on the same day that it had signed a voluntary licensing agreement with the Medicines Patent Pool, which would allow sub-licenses to produce generic drugs and supply up to 95 countries around the world. On the other hand, it will be necessary to wait for the European Medicines Agency to give its approval for marketing in France.

On November 5, the American laboratory revealed in a press release that it had stopped clinical trials of its drug which, associated with another antiviral, reduces the risk of severe forms by 89%, according to the first results. The purpose of this suspension was to speed up the application for marketing authorization for the drug in the United States. Indeed, the pharmaceutical company had indicated that it wanted to send the provisional data resulting from the first tests as soon as possible to the Food and Drug Administration, the American drug agency. Encouraging results which are timely, after the recent PfizerGate.

https://www.linternaute.com/actualite/g ... fficacite/

They got their name wrong !!

PAXCOVID would have sounded better! At least for all languages ​​of Latin origin

Bunch of morons of overpaid executives!

ps: my mom taught me that when you got ripped off once by a person *, you don't have to trust her the second time ... society-and-philosophy / human-societies-everything-is-trusted-t11776.html

* physical at the time but I add moral today

You have to see the bright side of things, even if it doesn't work or if it pisses you off as much as it "heals" you at least we will have a medoc and they will perhaps let go of the bunch with the vax

[Janic]

You have to see the bright side of things, even if it doesn't work or if it pisses you off as much as it "heals" you at least we will have a medoc and they will perhaps let go of the bunch with the vax

do not dream! Why abandon such a source of gains when both can increase them even more?

[Adrien (ex-nico239)]

You have to see the bright side of things, even if it doesn't work or if it pisses you off as much as it "heals" you at least we will have a medoc and they will perhaps let go of the bunch with the vax

do not dream! Why abandon such a source of gains when both can increase them even more?

I was talking about the health dictatorship

[Petrus]

The mRNA injections can only be done en masse by forcing people into it and from the government's point of view the injection justifies social control, they will not stop the injections and the pass that goes with them- same. Treatments are therefore only considered "in addition to vaccines" as it is written in the article.