智利科兴疫苗的结果出来了

老向牛逼,不管啥盘却叼得住!回国也能当个厅级干部。
 
建议每周打一针,估计10周后有效率能上90%:)


美国的疫苗效果只有1月好,2,3,4都不行。



Screenshot_20210407_184243.jpg
 
18岁以下人不打,再加上20%的美国人不愿接种。估计5,6万病例要持续一段时间了。
美国是因为开放了,不往上冲就不错了,看看加拿大,疫苗打的少,一波强劲反弹。
 
如何看待疫苗有效率,能不能比较各种疫苗的有效率?

 
老向和官方两人要是都变节了。

哎,意味着中国将投入巨资开始在北美抢mrna疫苗了,中国真要是开抢,哪个强得过?

加拿大人准备好雪上加霜吧。。。
什么叫变节,我只是在最初引用过一次100有效的说法。但是那也没错,我当时认为疫苗只要能产生抗体就是有效。 后来知道这里有效率的定义完全不是我想的那样。此后我再没有说过哪个疫苗更有效地话。全部都是对你发表的论据的非议。争论基本上都在疫苗的安全性上。我自始至终的观点都是mRNA疫苗是长期安全性不如灭火疫苗明朗或者说明确。事实也是如此。根据我所看到的报导,副作用方面灭活疫苗应该是最低的。
我觉得你们高兴的太早,离全面评价各种疫苗还远。新增病例大趋势上应该和疫苗有效率成某种比例关系,但是其他因素太多,科学上不构成充分条件。安全性问题更是没有科学的评估的基础。例如AZ的血栓问题渐渐的浮出水面。
别着急,让子弹飞一会儿。跳的太高容易让天花板撞断脖子。 :D
 
什么叫变节,我只是在最初引用过一次100有效的说法。但是那也没错,我当时认为疫苗只要能产生抗体就是有效。 后来知道这里有效率的定义完全不是我想的那样。此后我再没有说过哪个疫苗更有效地话。全部都是对你发表的论据的非议。争论基本上都在疫苗的安全性上。我自始至终的观点都是mRNA疫苗是长期安全性不如灭火疫苗明朗或者说明确。事实也是如此。根据我所看到的报导,副作用方面灭活疫苗应该是最低的。
我觉得你们高兴的太早,离全面评价各种疫苗还远。新增病例大趋势上应该和疫苗有效率成某种比例关系,但是其他因素太多,科学上不构成充分条件。安全性问题更是没有科学的评估的基础。例如AZ的血栓问题渐渐的浮出水面。
别着急,让子弹飞一会儿。跳的太高容易让天花板撞断脖子。 :D
100%有效无害,没法蹦得更高了。也就到这了。sorry
 

PFIZER-BIONTECH ANNOUNCE POSITIVE TOPLINE RESULTS OF PIVOTAL COVID-19 VACCINE STUDY IN ADOLESCENTS​

Wednesday, March 31, 2021 - 06:45am
  • In participants aged 12-15 years old, BNT162b2 demonstrated 100% efficacy and robust antibody responses, exceeding those reported in trial of vaccinated 16-25 year old participants in an earlier analysis, and was well tolerated
  • The companies plan to submit these data to the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA) as soon as possible to request expansion of the Emergency Use Authorization (EUA) and EU Conditional Marketing Authorization for BNT162b2
  • The companies also provided an update on the Phase 1/2/3 study of BNT162b2 in children aged 6 months to 11 years
NEW YORK & MAINZ, Germany--(BUSINESS WIRE)-- Pfizer Inc. (NYSE: PFE) and BioNTech SE (Nasdaq: BNTX) today announced that, in a Phase 3 trial in adolescents 12 to 15 years of age with or without prior evidence of SARS-CoV-2 infection, the Pfizer-BioNTech COVID-19 vaccine BNT162b2 demonstrated 100% efficacy and robust antibody responses, exceeding those recorded earlier in vaccinated participants aged 16 to 25 years old, and was well tolerated. These are topline results from a pivotal Phase 3 trial in 2,260 adolescents.

 

PFIZER-BIONTECH ANNOUNCE POSITIVE TOPLINE RESULTS OF PIVOTAL COVID-19 VACCINE STUDY IN ADOLESCENTS​

Wednesday, March 31, 2021 - 06:45am
  • In participants aged 12-15 years old, BNT162b2 demonstrated 100% efficacy and robust antibody responses, exceeding those reported in trial of vaccinated 16-25 year old participants in an earlier analysis, and was well tolerated
  • The companies plan to submit these data to the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA) as soon as possible to request expansion of the Emergency Use Authorization (EUA) and EU Conditional Marketing Authorization for BNT162b2
  • The companies also provided an update on the Phase 1/2/3 study of BNT162b2 in children aged 6 months to 11 years
NEW YORK & MAINZ, Germany--(BUSINESS WIRE)-- Pfizer Inc. (NYSE: PFE) and BioNTech SE (Nasdaq: BNTX) today announced that, in a Phase 3 trial in adolescents 12 to 15 years of age with or without prior evidence of SARS-CoV-2 infection, the Pfizer-BioNTech COVID-19 vaccine BNT162b2 demonstrated 100% efficacy and robust antibody responses, exceeding those recorded earlier in vaccinated participants aged 16 to 25 years old, and was well tolerated. These are topline results from a pivotal Phase 3 trial in 2,260 adolescents.

牛,太牛了!
 

PFIZER-BIONTECH ANNOUNCE POSITIVE TOPLINE RESULTS OF PIVOTAL COVID-19 VACCINE STUDY IN ADOLESCENTS​

Wednesday, March 31, 2021 - 06:45am
  • In participants aged 12-15 years old, BNT162b2 demonstrated 100% efficacy and robust antibody responses, exceeding those reported in trial of vaccinated 16-25 year old participants in an earlier analysis, and was well tolerated
  • The companies plan to submit these data to the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA) as soon as possible to request expansion of the Emergency Use Authorization (EUA) and EU Conditional Marketing Authorization for BNT162b2
  • The companies also provided an update on the Phase 1/2/3 study of BNT162b2 in children aged 6 months to 11 years
NEW YORK & MAINZ, Germany--(BUSINESS WIRE)-- Pfizer Inc. (NYSE: PFE) and BioNTech SE (Nasdaq: BNTX) today announced that, in a Phase 3 trial in adolescents 12 to 15 years of age with or without prior evidence of SARS-CoV-2 infection, the Pfizer-BioNTech COVID-19 vaccine BNT162b2 demonstrated 100% efficacy and robust antibody responses, exceeding those recorded earlier in vaccinated participants aged 16 to 25 years old, and was well tolerated. These are topline results from a pivotal Phase 3 trial in 2,260 adolescents.


什么破玩意,不信,我只信国药集团的灭活!中国药业可信度贼高。100%可信!打死也不用洋人的疫苗!
 
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