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Novavax (Nuvaxovid) XBB.1.5 COVID-19疫苗是含佐劑Matrix-M之SARS-CoV-2 (Omicron XBB.1.5) 重組棘蛋白之蛋白質次單元疫苗,用於預防COVID-19,目前國內核准Novavax (Nuvaxovid) XBB.1.5疫苗,適用於12歲以上,每劑接種0.5 mL。 目前依我國衛生福利部傳染病防治諮詢會預防接種組(ACIP)建議,接種時程與間隔如下: 註:目前國內購得XBB.1.5疫苗有2種廠牌(Moderna及Novavax),僅需擇一疫苗接種。 疫苗接種禁忌與接種前注意事項. 接種禁忌:對於疫苗成分有嚴重過敏反應史,或先前接種本項疫苗劑次發生嚴重過敏反應者,不予接種。 注意事項:
2023年10月16日 · October 16, 2023. 4 min read. Is the Novavax COVID Vaccine Better Than mRNA Vaccines? What We Know So Far. Novavax’s protein-based vaccine is the latest FDA-authorized COVID booster...
The Novavax COVID-19 vaccine, sold under the brand names Nuvaxovid and Covovax, [1] among others, is a subunit COVID-19 vaccine developed by Novavax and the Coalition for Epidemic Preparedness Innovations (CEPI). [29] Medical uses. The Novavax COVID‑19 vaccine is indicated for active immunization to prevent COVID‑19 caused by SARS-CoV-2. [4]
疫苗概述. Novavax (Nuvaxovid) XBB.1.5 COVID-19疫苗 是含佐劑Matrix-M之SARS-CoV-2 (OmicronXBB.1.5) 重組棘蛋白之蛋白質次單元疫苗，用於預防COVID-19，目前國內核准Novavax XBB.1.5疫苗，適用於12歲以上，每劑接種0.5mL。 目前依我國衛生福利部傳染病防治諮詢會預防接種組 (ACIP)建議，接種時程與間隔如下: 註: 目前國內購得XBB.1.5疫苗有2種廠牌（Moderna及Novavax），僅需擇一疫苗接種。 接種途徑為肌肉注射. 安全性及保護效果. 本疫苗不含可複製之SARS-CoV-2病毒顆粒，不會因為接種本疫苗而罹患COVID-19。
- Who Can Take This Vaccine?
- Should Pregnant and Breastfeeding Women Be Vaccinated?
- Who Is The Vaccine Not Recommended for?
- Is It Safe?
- How Efficacious Is The Vaccine?
- What Is The Recommended Dosage?
- Can This Vaccine Be ‘Mixed and Matched’ with Other Vaccines?
- Does It Prevent Infection and Transmission?
- Does It Work Against New Variants of Sars-Cov-2 Virus?
- How Does This Vaccine Compare to Other Covid-19 Vaccines Already in use?
The vaccine is safe and effective for all individuals aged 12 and above. In line with the WHO Prioritization Roadmap and the WHO Values Framework, older adults, health workers and immunocompromised persons should be prioritised. Adolescents with moderate to severe immunocompromising conditions belong to the highest priority-use group. The Novavax v...
Emerging post-introduction pharmacovigilance data relating to the use of NVX-CoV2373 in pregnant women have not identified any pregnancy-related safety concerns and based on previous evidence from other protein-based vaccines during pregnancy, efficacy is expected to be comparable to non-pregnant women of a similar age. WHO has identified pregnant ...
The vaccine is not recommended for people younger than 12 years of age. Individuals with a history of anaphylaxis to any component of the vaccine should not take it. Persons with acute PCR-confirmed COVID-19 should not be vaccinated until after they have recovered from acute illness and the criteria for ending isolation have been met. Anyone with a...
SAGE has thoroughly assessed the data on the safety and efficacy of the vaccine and has recommended its use for people aged 12 and above. The WHO EUL process also evaluates the quality of manufacturing along with safety and efficacy. Very rare serious adverse events of myocarditis and pericarditis have been observed though cases typically occurred ...
The efficacy of Novavax (NVX-CoV2373) has been assessed in three Phase 2 and Phase 3 trials. Of the two Phase 3 trials, both found that the efficacy of the vaccine against mild, moderate, and severe disease is 90%. The efficacy of Novavax(NVX-CoV2373) in adolescents 12 to 17 years of age was evaluated in an interim analysis of the paediatric expans...
SAGE recommends the use of the Novavax (NVX-CoV2373) vaccine as 2 doses (0.5 ml) given intramuscularly. An 8-week interval is recommended between primary series doses of NVX-CoV2373. A first booster dose is recommended 4-6 months after the completion of the primary series. In accordance with the WHO Prioritization Roadmap, the highest priority-use ...
SAGE accepts two heterologous doses of WHO EUL COVID-19 vaccines as a complete primary series. However, there is limited evidence available on the use of Novavax (NVX-CoV2373) in a heterologous schedule.
As there is not currently sufficient evidence to date to evaluate the impact of the vaccine on transmission, public health and social measures must continue, including use of face masks, physical distancing, handwashing, appropriate ventilation, and other measures as appropriate in particular settings, depending on the COVID-19 epidemiology and pot...
In a Phase 3 study conducted in the USA and Mexico during a period in which multiple variants (Alpha, Beta and Delta) were in circulation, vaccine efficacy against mild, moderate, or severe COVID-19 was 90%. In view of these findings, WHO recommends the use of Novavax (NVX-CoV2373) vaccine according to the WHO Prioritization Roadmap, even if curren...
It is impossible to compare vaccine head-to-head due to the different approaches taken in designing the respective studies, but overall, all of the vaccines that have achieved WHO Emergency Use Listing are highly effective in preventing severe disease and hospitalization due to COVID-19. This webpage was updated on 28 September 2022 to reflect upda...
2023年11月28日 · GAITHERSBURG, Md., Nov. 28, 2023 /PRNewswire/ -- Novavax, Inc. (Nasdaq: NVAX), a global company advancing protein-based vaccines with its Matrix-M™ adjuvant, today announced that Nuvaxovid™ XBB.1.5 COVID-19 Vaccine (NVX-CoV2601) has been granted Emergency Use Listing (EUL) by the World Health Organization (WHO) for active immunization to prevent...
Novavax. (Nuvaxovid) COVID-19疫苗介紹. 疫苗包裝、外觀. 外包裝:多劑型,10 劑(5 mL)/ 瓶。 10 瓶1盒。 不需稀釋. 外觀:呈現無色至淡黃色,透明至微乳白色狀態. 版次:2022/7/5. 疫苗簡介-1. 疫苗成分. • 每劑0.5 mL 含有5 μg SARS-COV-2 重組棘蛋白以及佐劑Matrix-M。 適用年齡. • 18歲以上. 疫苗保護力. 依據目前臨床試驗結果資料顯示( 非omicron 變異株), 本疫苗對於年滿18歲以上之青少年及成人受試者接種完成2 劑接種7 天後預防有症狀感染之有效性約90.4%1。
