天啊,搞了半天莫德納疫苗在今天以前一直都沒有被FDA正式批准啊!接種了該疫苗的人此前知道不?

TianK

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FDA全面批准莫德納新冠疫苗

最後更新 2022年2月1日
美國之音



FDA全面批准莫德納新冠疫苗

美國食品藥品管理局(FDA)星期一(1月31日)全面批准美國製藥公司莫德納(Moderna)的COVID-19疫苗,該疫苗將以Spikevax的品牌營銷。

自從2020年12月以來,莫德納疫苗已經按照FDA的緊急使用授權而在美國和世界各地廣泛使用。這是FDA全面批准的第二個COVID-19疫苗,該機構在2021年8月全面批准了輝瑞( Pfizer)的COVID-19疫苗。

FDA代理局長珍妮特·伍德科克(Janet Woodcock)在一項聲明中說,全面批准該疫苗是抗擊COVID-19大流行病的關鍵一步。她說,雖然已按照緊急使用授權接種了數億劑的莫德納疫苗,但是她了解“對有些人來說,FDA批准該疫苗有可能為接種疫苗的決定注入更多的信心”。

伍德科克說,公眾可以放心,莫德納疫苗“在安全性、有效性和生產質量方面滿足FDA有關任何在美國獲批使用的疫苗的高標準”。

70多個國家已經批准使用莫德納疫苗,包括英國、加拿大、日本和歐盟國家。

(本文參考了美聯社與路透社的報導。)
 

Omicron

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奇怪,难道你不知道正式批准的疫苗你打不到,无论是辉瑞还是莫纳德

你被打的都是紧急使用的疫苗,后果自负的
 

TianK

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奇怪,难道你不知道正式批准的疫苗你打不到,无论是辉瑞还是莫纳德

你被打的都是紧急使用的疫苗,后果自负的

輝瑞肯定是去年被正式批准了的
 

Omicron

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輝瑞肯定是去年被正式批准了的
批准你也打不到

连军队打的都是紧急使用的

原因是正式批准的打死厂家要赔偿,紧急使用的打死不赔偿,就这么简单
 

breaveheart

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去年晚些时候辉瑞得到了FDA正式授权。好像早于5-11岁打疫苗。
 

Omicron

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正式批准的原因就是为了给军队打疫苗

因为规定军队打的疫苗,必须正式批准。

实际打的还是紧急使用的疫苗

这是左左玩的移花接木的手段,美国人敢怒不敢言,美国人挺怂
 

lindamy

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FDA全面批准莫德納新冠疫苗

最後更新 2022年2月1日
美國之音



FDA全面批准莫德納新冠疫苗

美國食品藥品管理局(FDA)星期一(1月31日)全面批准美國製藥公司莫德納(Moderna)的COVID-19疫苗,該疫苗將以Spikevax的品牌營銷。

自從2020年12月以來,莫德納疫苗已經按照FDA的緊急使用授權而在美國和世界各地廣泛使用。這是FDA全面批准的第二個COVID-19疫苗,該機構在2021年8月全面批准了輝瑞( Pfizer)的COVID-19疫苗。

FDA代理局長珍妮特·伍德科克(Janet Woodcock)在一項聲明中說,全面批准該疫苗是抗擊COVID-19大流行病的關鍵一步。她說,雖然已按照緊急使用授權接種了數億劑的莫德納疫苗,但是她了解“對有些人來說,FDA批准該疫苗有可能為接種疫苗的決定注入更多的信心”。

伍德科克說,公眾可以放心,莫德納疫苗“在安全性、有效性和生產質量方面滿足FDA有關任何在美國獲批使用的疫苗的高標準”。

70多個國家已經批准使用莫德納疫苗,包括英國、加拿大、日本和歐盟國家。

(本文參考了美聯社與路透社的報導。)
你什么时候打的什么疫苗?当时全面批准了吗?
 

lindamy

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Pfizer logo
BioNTech logo


VACCINE NAME: Comirnaty (also known as tozinameran or BNT162b2)
EFFICACY: 91%
DOSE: 2 doses, 3 weeks apart
TYPE: Muscle injection
STORAGE: Freezer storage only at –13°F to 5°F (–25°C to –15°C)

On Nov. 9, 2020, New York-based Pfizer and the German company BioNTech made history by announcing that their coronavirus vaccine had an efficacy rate of over 90 percent, far surpassing expectations. It was the first time anyone had found such evidence. Just over a month later, on Dec. 11, the Food and Drug Administration granted the vaccine, known as Comirnaty, the first emergency use authorization ever given by the United States to a coronavirus vaccine. On Aug. 23, 2021, the F.D.A. granted full approval to Comirnaty, for people 16 and older, and it now has an emergency authorization for children as young as five. On Sep. 22, the F.D.A. authorized a third dose as a booster for people age 65 and older, and other populations at high risk. It expanded the authorization for adolescents 12 through 15 on Jan. 3, 2022. On Nov. 2, Pfizer predicted that the companies would make roughly 3 billion doses in 2021.

-------------------------------------------------------------------------

Moderna logo
National Institutes of Health logo


VACCINE NAME: mRNA-1273 or Spikevax
EFFICACY: Preventing Covid-19 illness: 93.2%. Preventing severe disease: 98.2%.
DOSE: 2 doses, 4 weeks apart
TYPE: Muscle injection
STORAGE: 30 days with refrigeration, 6 months at –4°F (–20°C)

On Dec. 18., 2020, the F.D.A. gave emergency use authorization for a vaccine made by the Boston-based company Moderna. The Moderna vaccine, known as Spikevax or mRNA-1273, was the second to be authorized by the F.D.A., coming a week after Comirnaty, the vaccine made by Pfizer and BioNTech. In 2021, Moderna shipped over 800 million doses worldwide. The F.D.A. gave full approval to Spikevax on Jan. 31, 2022.

 

ccc

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Pfizer logo
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VACCINE NAME: Comirnaty (also known as tozinameran or BNT162b2)
EFFICACY: 91%
DOSE: 2 doses, 3 weeks apart
TYPE: Muscle injection
STORAGE: Freezer storage only at –13°F to 5°F (–25°C to –15°C)

On Nov. 9, 2020, New York-based Pfizer and the German company BioNTech made history by announcing that their coronavirus vaccine had an efficacy rate of over 90 percent, far surpassing expectations. It was the first time anyone had found such evidence. Just over a month later, on Dec. 11, the Food and Drug Administration granted the vaccine, known as Comirnaty, the first emergency use authorization ever given by the United States to a coronavirus vaccine. On Aug. 23, 2021, the F.D.A. granted full approval to Comirnaty, for people 16 and older, and it now has an emergency authorization for children as young as five. On Sep. 22, the F.D.A. authorized a third dose as a booster for people age 65 and older, and other populations at high risk. It expanded the authorization for adolescents 12 through 15 on Jan. 3, 2022. On Nov. 2, Pfizer predicted that the companies would make roughly 3 billion doses in 2021.

-------------------------------------------------------------------------

Moderna logo
National Institutes of Health logo


VACCINE NAME: mRNA-1273 or Spikevax
EFFICACY: Preventing Covid-19 illness: 93.2%. Preventing severe disease: 98.2%.
DOSE: 2 doses, 4 weeks apart
TYPE: Muscle injection
STORAGE: 30 days with refrigeration, 6 months at –4°F (–20°C)

On Dec. 18., 2020, the F.D.A. gave emergency use authorization for a vaccine made by the Boston-based company Moderna. The Moderna vaccine, known as Spikevax or mRNA-1273, was the second to be authorized by the F.D.A., coming a week after Comirnaty, the vaccine made by Pfizer and BioNTech. In 2021, Moderna shipped over 800 million doses worldwide. The F.D.A. gave full approval to Spikevax on Jan. 31, 2022.


疫苗本身有区别没有?
 

Omicron

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疫苗本身有区别没有?
没区别。这么大的事情,你们难道一直都不知道?

辉瑞对自己的疫苗没啥信心,要规避法律风险,军队的规定估计有啥法律漏洞,被左左串通辉瑞和FDA,钻了空子。否则也没法强制军队打疫苗
 

wei_cheng

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一楼完全不懂什么是 Emergency Use Authorization (EUA) 阶段
你什么时候打的什么疫苗?当时全面批准了吗?
 

uglyducking

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Pfizer logo
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VACCINE NAME: Comirnaty (also known as tozinameran or BNT162b2)
EFFICACY: 91%
DOSE: 2 doses, 3 weeks apart
TYPE: Muscle injection
STORAGE: Freezer storage only at –13°F to 5°F (–25°C to –15°C)

On Nov. 9, 2020, New York-based Pfizer and the German company BioNTech made history by announcing that their coronavirus vaccine had an efficacy rate of over 90 percent, far surpassing expectations. It was the first time anyone had found such evidence. Just over a month later, on Dec. 11, the Food and Drug Administration granted the vaccine, known as Comirnaty, the first emergency use authorization ever given by the United States to a coronavirus vaccine. On Aug. 23, 2021, the F.D.A. granted full approval to Comirnaty, for people 16 and older, and it now has an emergency authorization for children as young as five. On Sep. 22, the F.D.A. authorized a third dose as a booster for people age 65 and older, and other populations at high risk. It expanded the authorization for adolescents 12 through 15 on Jan. 3, 2022. On Nov. 2, Pfizer predicted that the companies would make roughly 3 billion doses in 2021.

-------------------------------------------------------------------------

Moderna logo
National Institutes of Health logo


VACCINE NAME: mRNA-1273 or Spikevax
EFFICACY: Preventing Covid-19 illness: 93.2%. Preventing severe disease: 98.2%.
DOSE: 2 doses, 4 weeks apart
TYPE: Muscle injection
STORAGE: 30 days with refrigeration, 6 months at –4°F (–20°C)

On Dec. 18., 2020, the F.D.A. gave emergency use authorization for a vaccine made by the Boston-based company Moderna. The Moderna vaccine, known as Spikevax or mRNA-1273, was the second to be authorized by the F.D.A., coming a week after Comirnaty, the vaccine made by Pfizer and BioNTech. In 2021, Moderna shipped over 800 million doses worldwide. The F.D.A. gave full approval to Spikevax on Jan. 31, 2022.

FDA罔顾疫苗无用的事实居然还是approve了莫得纳和肥泽的疫苗,真是官商勾结一起残害鱼肉百姓啊:shale::kan::wall::buttrock:
 

uglyducking

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没区别。这么大的事情,你们难道一直都不知道?

辉瑞对自己的疫苗没啥信心,要规避法律风险,军队的规定估计有啥法律漏洞,被左左串通辉瑞和FDA,钻了空子。否则也没法强制军队打疫苗
打倒FDA!:buttrock:
 

TianK

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疫苗本身有区别没有?

這問題你問藥廠去,最好還問一下FDA:為啥最後批准要一直拖到今天,之前究竟有啥顧慮?是實驗數據不夠全?還是藥廠仍有些事情沒有解釋清楚?
 

Omicron

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這問題你問藥廠去,最好還問一下FDA:為啥最後批准要一直拖到今天,之前究竟有啥顧慮?是實驗數據不夠全?還是藥廠仍有些事情沒有解釋清楚?
你们对这些事情一点都不知道,奇怪?

正式批准的疫苗,重新做了临床实验,东西和紧急使用的疫苗一样。临床实验的时候是英国变种,实验结果不好,打疫苗和不打疫苗的,得新冠死亡人数一样,等于没有防止重症的作用。疫苗组最后死的比对照组还多,不少还是心肌炎,和一些奇怪的毛病,这还只是疫苗后几个星期的结果,按照规定要公布半年的结果

辉瑞不愿意公布详细数据,所以现在在打官司
 
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