当初的一念之仁,一次脑子清楚的判断,如今回报了。

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打了两针Moderna的人,再来第三针?
 

lindamy

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打了两针Moderna的人,再来第三针?
大多数一般人用不着,65岁以上,18-64岁从事新冠高危职业,或者有严重疾病,免疫缺陷等人群。

(CNN)Vaccine advisers to the US Food and Drug Administration voted unanimously Thursday to recommend emergency use authorization of a booster dose of Moderna's Covid-19 vaccine.

The FDA's Vaccines and Related Biological Products Advisory Committee agreed use of a booster dose would be safe and effective in some people six months out from their primary series.

Moderna had asked for emergency use authorization for a half dose of its vaccine to be used as a booster for certain people.
All 19 members of the committee supported the question:

Do available data support the safety and effectiveness of Moderna Covid-19 Vaccine for use under EUA as a booster dose (50 mcg mRNA-1273) at least 6 months after completion of a primary series in the following populations:

Individuals 65 years of age and older

Individuals 18 through 64 years of age at high risk of severe Covid-19, and

Individuals 19 through 64 years of age whose frequent institutional or occupational exposure to SARS-Covid-2 puts them at high risk of serious complications of COVID-19 including severe COVID-19


Moderna urges FDA to authorize a half-size booster dose of its Covid-19 vaccine for some adults

Moderna urges FDA to authorize a half-size booster dose of its Covid-19 vaccine for some adults

Moderna's request mirrored the groups authorized to receive a booster dose of Pfizer's mRNA vaccine. Third doses of the Moderna and Pfizer Covid-19 vaccines are already authorized for some immunocompromised people.

The Vaccines and Related Biological Products Advisory Committee meeting will continue Friday, when members are expected to vote on boosters for the Johnson & Johnson vaccine, and will hear a presentation on mix-and-match vaccines.

The FDA's committee of independent advisers typically discusses and makes recommendations to the agency around vaccine authorizations and approvals, and the agency then makes the final decision about whether to OK a vaccine.

If the FDA gives emergency use authorization to Moderna boosters, vaccine advisers to the US Centers for Disease Control and Prevention will meet to discuss which groups to recommend them to. Typically, shots can be administered once the CDC director signs off on the recommendation.

CDC's Advisory Committee on Immunization Practices is already scheduled to meet to discuss boosters from 10 a.m. to 5 p.m. ET October 20-21.
 

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虽然最终决定权在CDC,至少FDA没有否决Moderna的半剂量加强针。。。

今天的表决19:0通过。

估计CDC对Moderna的决定,和辉瑞加强针的结果一样,对老年人和免疫不全的人使用加强针。否则执行起来太乱了。
 
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ottawa_tj

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打了两针Moderna的人,再来第三针?

Moderna的加强针剂量比普通针减半,打的时候要注意看一下。
 

贵圈

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哈哈。我肯定不需要了。两针已经够我受得了
 

贵圈

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哈哈,技术上,已经否定了。不符合标准

不过呢,标准,对于官僚来说,就是任人摆弄妓女

还有为官僚和妓女欢呼推背的,真够逗得。

还马甲590。

不如马甲龟公零。
 

一心无住

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打了两针Moderna的人,再来第三针?
以色列2针都不算打过疫苗了,第三针才算。以后就是第n针才算。
 

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Moderna的加强针剂量比普通针减半,打的时候要注意看一下。

不知道我们这里什么时候开始打第三针。
 

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以色列2针都不算打过疫苗了,第三针才算。以后就是第n针才算。

感冒疫苗不是每年都有么。
 

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感冒疫苗不是每年都有么。
因为新冠病毒比感冒病毒变异性还强,所以每针的间隔不是一年,是几个月。
 

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因为新冠病毒比感冒病毒变异性还强,所以每针的间隔不是一年,是几个月。

一针没打,不是也好好的么。
 

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