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U.S. CDC and ACIP Recommend Additional COVID-19 Vaccine Dose for Older Individuals and Those Who Are Immunocompromised

U.S. CDC and ACIP Recommend Additional COVID-19 Vaccine Dose for Older Individuals and Those Who Are Immunocompromised

美国疾病控制和预防中心以及疾病预防和控制咨询委员会建议对年长者和免疫功能受损者接种额外的COVID-19生物-疫苗剂。
诺瓦瓦克斯医药 ·  10/24 00:00

The U.S. Centers for Disease Control and Prevention (CDC) has endorsed the CDC Advisory Committee on Immunization Practices' (ACIP) recommendations for:

美国疾病控制和预防中心(CDC)已经支持疾病控制和预防咨询委员会(ACIP)关于以下内容的建议:

  1. A second dose of 2024-2025 COVID-19 vaccine for adults aged 65 years and older six months after the first dose.
  2. A second dose of 2024-2025 COVID-19 vaccine for people aged six months and older who are moderately or severely immunocompromised six months after the first dose.
  3. Additional doses (i.e., three or more) for people who are moderately or severely immunocompromised in consultation with a healthcare provider.
  1. 针对65岁及以上成年人,2024-2025年的新冠疫苗接种第二剂,间隔首剂六个月。
  2. 针对六个月及以上年龄的免疫功能中度或严重受损的人群,2024-2025年的新冠疫苗接种第二剂,间隔首剂六个月。
  3. 针对免疫功能中度或严重受损的人群,可以额外接种(即三剂或更多),需咨询医疗保健提供者。

Doses of the Novavax COVID-19 Vaccine, Adjuvanted (2024-2025 Formula) (NVX-CoV2705) are currently available at more than 30,000 locations, including major pharmacy retailers, regional grocers and independent pharmacies across the U.S. Doses are also available at physicians' offices and public health clinics, through Vaccines for Children, Federally Qualified Health Centers, Indian Health Services and the U.S. Department of Defense, and through agreements with Group Purchasing Organizations. The best source for finding our vaccine is us.novavaxcovidvaccine.com/vaccine-finder.

诺瓦瓦克斯医药新冠疫苗,含佐剂(2024-2025配方)(NVX-CoV2705)目前在美国的30000多个地点提供,包括主要药店、区域性食品零售商和独立药房。此外,在医生诊所和公共卫生诊所、儿童疫苗计划、联邦合格的卫生中心、印第安人卫生服务以及美国国防部,以及与集团采购组织达成协议的地方也提供接种。查找我们疫苗的最佳途径,请访问us.novavaxcovidvaccine.com/vaccine-finder。

While the recommendations focus on additional protection for older individuals and those who are immunocompromised, vaccination continues to be the best source for protection against COVID-19 for all those who are eligible.

尽管这些建议侧重于为老年人和免疫受损人群提供额外保护,但接种继续是所有符合条件的人群对抗新冠疫情的最佳途径。

AUTHORIZED USE IN THE U.S.

在美国被授权使用。

Novavax COVID-19 Vaccine, Adjuvanted (2024-2025 Formula) has not been approved or licensed by the U.S. Food and Drug Administration (FDA) but has been authorized for emergency use by the FDA, under an Emergency Use Authorization (EUA) to prevent Coronavirus Disease 2019 (COVID-19) for use in individuals 12 years of age and older. Refer to the full Fact Sheet for information about the Novavax COVID-19 Vaccine, Adjuvanted.

诺瓦瓦克斯医药新冠疫苗,含佐剂(2024-2025配方)尚未获得美国食品药品监督管理局(FDA)批准或许可,但已获得FDA紧急使用授权,在12岁及以上人群中用于预防2019冠状病毒病(COVID-19)。有关诺瓦瓦克斯医药新冠疫苗,含佐剂的详细信息,请参阅完整事实说明书。

The EUA of this product will remain in effect for the duration of the COVID-19 EUA declaration justifying emergency use of the product, unless the authorization is revoked sooner.

该产品的紧急使用授权将在COVID-19紧急使用授权声明的有效期内生效,除非授权提前被撤销。

VACCINE AUTHORIZATION (U.S.)

疫苗授权(美国)

Novavax COVID-19 Vaccine, Adjuvanted (2024-2025 Formula) is indicated for active immunization to prevent coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in individuals 12 years of age and older.

诺瓦瓦克斯医药的COVID-19疫苗(2024-2025年配方)用于主动免疫,以预防由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)引起的2019年冠状病毒病(COVID-19),适用于12岁及以上的个体。

IMPORTANT SAFETY INFORMATION

重要安全信息

Contraindications

忌用症。

  • Do not administer the Novavax COVID-19 Vaccine, Adjuvanted to individuals with a known history of a severe allergic reaction (e.g., anaphylaxis) to any component of the Novavax COVID-19 Vaccine, Adjuvanted.
  • 不要给有已知对诺瓦瓦克斯医药COVID-19疫苗(2024-2025年配方)的任何成分发生严重过敏反应(例如,过敏性休克)的个体接种。

Warnings and Precautions

警告和注意事项。

  • Management of Acute Allergic Reactions: Appropriate medical treatment must be immediately available to manage potential anaphylactic reactions following administration of the Novavax COVID-19 Vaccine, Adjuvanted.
  • Myocarditis and Pericarditis: Clinical trials data provide evidence for increased risks of myocarditis and pericarditis following administration of Novavax COVID-19 Vaccine, Adjuvanted.
  • Syncope (fainting): may occur in association with administration of injectable vaccines. Procedures should be in place to avoid injury from fainting.
  • Altered Immunocompetence: Immunocompromised persons, including individuals receiving immunosuppressant therapy, may have a diminished immune response to the Novavax COVID-19 Vaccine, Adjuvanted.
  • Limitations of Vaccine Effectiveness: The Novavax COVID-19 Vaccine, Adjuvanted may not protect all vaccine recipients.
  • 必须立即提供适当的医疗处理以处理接种诺瓦瓦克斯医药 COVID-19 疫苗后可能发生的过敏反应。
  • 心肌炎和心包炎:临床试验数据显示接种诺瓦瓦克斯医药 COVID-19 疫苗后心肌炎和心包炎风险增加。
  • 晕厥(昏倒):在接种注射疫苗时可能发生晕厥。应制定措施以避免昏倒导致的伤害。
  • 免疫能力改变:包括正在接受免疫抑制疗法的免疫功能受损者,对诺瓦瓦克斯医药 COVID-19 疫苗的免疫反应可能减弱。
  • 疫苗效果的局限性:诺瓦瓦克斯医药 COVID-19 疫苗可能无法保护所有接种者。

Adverse Reactions

副作用

Solicited adverse reactions included: Injection site pain/tenderness, fatigue/malaise, muscle pain, headache, joint pain, nausea/vomiting, injection site redness, injection site swelling and fever.

征询的不良反应包括:注射部位疼痛/疼痛、疲劳/倦怠、肌肉疼痛、头痛、关节疼痛、恶心/呕吐、注射部位红肿、注射部位肿胀和发热。

Reporting Adverse Events and Vaccine Administration Errors

报告不良事件和疫苗接种错误

The vaccination provider is responsible for mandatory reporting of certain adverse events to the Vaccine Adverse Event Reporting System (VAERS) online at , by calling 1-800-822-7967 or send an email to info@vaers.org.

疫苗供应商负责将某些不良事件强制性报告给疫苗不良事件报告系统(VAERS),您可以在线报告,网址是,也可以拨打1-800-822-7967进行电话报告,或者发送电子邮件至info@vaers.org。

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