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CONVENIENT STORAGE AND ADMINISTRATION WITH NUVAXOVID.1


NUVAXOVID arrives ready to use in prefilled syringes, with no freezing or thawing needed1

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Ready to use—no dilution, mixing, or thawing required

Ships in a carton of 10 prefilled syringes, each containing 1 dose of 0.5 mL

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Store in a standard refrigerator

Store prefilled syringes between 2 to 8 °C (36 to 46 °F)

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Do not freeze. Protect from light.

Only store prefilled syringes in a standard refrigerator. Store in original carton to protect from light.

Follow the CDC-recommended dosing schedule when administering NUVAXOVID1-3

For patients aged 65+

Vaccinated with primary series of NUVAXOVID or with any other COVID-19 vaccine

  • NUVAXOVID is administered intramuscularly as a single 0.5 mL dose at least 2 months after receipt of the previous vaccine dose1
  • ACIP recommends patients should receive an additional dose 6 months after the previous dose (minimum interval of 2 months)2

Not previously vaccinated with any COVID-19 vaccine

  • NUVAXOVID is administered intramuscularly as a single 0.5 mL dose1
  • ACIP recommends patients should receive an additional dose 6 months after the previous dose (minimum interval of 2 months)2

For patients aged 12-64 with ≥1 underlying condition

Vaccinated with primary series of NUVAXOVID or with any other COVID-19 vaccine

  • NUVAXOVID is administered intramuscularly as a single 0.5 mL dose at least 2 months after receipt of the previous vaccine dose1

Not previously vaccinated with any COVID-19 vaccine

  • NUVAXOVID is administered intramuscularly as a single 0.5 mL dose

Are your high-risk patients eligible for NUVAXOVID?

NUVAXOVID is also indicated for individuals 12 through 64 years who have at least one underlying condition that puts them at high risk for severe outcomes from COVID-19.1

The NUVAXOVID pivotal trial included patients who were high risk for COVID-19 due to underlying conditions, including chronic lung disease, cardiovascular disease, chronic liver disease, severe obesity, and diabetes.1

You can access the FDA's policy position on COVID-19 vaccination to see the list of medical conditions that increase risk of severe COVID-19. For further information. consult your national and local health authorities.

 

NUVAXOVID is the only non-mRNA, protein-based COVID-19 vaccine option you can offer to eligible patients regardless of the previous COVID-19 vaccines they received.1

 

You can easily order NUVAXOVID for your practice today!

Find COVID-19 resources for you and your patients.

INDICATION

NUVAXOVID is a vaccine indicated for active immunization to prevent coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). NUVAXOVID is approved for use in individuals who are:

  • 65 years of age and older, or
  • 12 years through 64 years of age with at least one underlying condition that puts them at high risk for severe outcomes from COVID-19.

IMPORTANT SAFETY INFORMATION

CONTRAINDICATION
Do not administer NUVAXOVID to individuals with a known history of severe allergic reaction (e.g., anaphylaxis) to any component of NUVAXOVID or to individuals who had a severe allergic reaction (e.g.,anaphylaxis) following a previous dose of NUVAXOVID

MANAGEMENT OF ACUTE ALLERGIC REACTIONS
Appropriate medical treatment must be immediately available to manage potential anaphylactic reactions following administration of NUVAXOVID

MYOCARDITIS AND PERICARDITIS
Clinical trials data provide evidence for increased risks of myocarditis and pericarditis following administration of NUVAXOVID. There have been post-marketing reports of myocarditis and pericarditis following administration of NUVAXOVID

SYNCOPE
Syncope (fainting) may occur in association with administration of injectable vaccines, including NUVAXOVID. Procedures should be in place to avoid injury from fainting

ALTERED IMMUNOCOMPETENCE
Immunocompromised persons, including individuals receiving immunosuppressive therapy, may have a diminished immune response to NUVAXOVID

COMMON ADVERSE REACTIONS
The most commonly reported (> 10%) solicited adverse reactions included: injection site pain/tenderness, fatigue/malaise, muscle pain, headache, nausea/vomiting, fever, and joint pain

INDICATION

IMPORTANT SAFETY INFORMATION

References

1. NUVAXOVID. Prescribing Information. Novavax, Inc. 2. Roper LE, Godfrey M, Link-Gelles R, et al. Use of additional doses of 2024-2025 COVID-19 vaccine for adults aged ≥65 years and persons aged ≥6 months with moderate or severe immunocompromise: recommendations of the Advisory Committee on Immunization Practices—United States, 2024. MMWR Morb Mortal Wkly Rep. 2024;73(49):1118-1123. 3. Panagiotakopoulos L, Moulia DL, Godfrey M, et al. Use of COVID-19 vaccines for persons aged ≥6 months: recommendations of the Advisory Committee on Immunization Practices—United States, 2024-2025. MMWR Morb Mortal Wkly Rep. 2024 Sep 19;73(37):819-824. doi:10.15585/mmwr. mm7337e2

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